TWI471619B - Optical fiber and its manufacturing method - Google Patents
Optical fiber and its manufacturing method Download PDFInfo
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- TWI471619B TWI471619B TW99122624A TW99122624A TWI471619B TW I471619 B TWI471619 B TW I471619B TW 99122624 A TW99122624 A TW 99122624A TW 99122624 A TW99122624 A TW 99122624A TW I471619 B TWI471619 B TW I471619B
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- Taiwan
- Prior art keywords
- optical fiber
- core portion
- polymer
- weight
- tcema
- Prior art date
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- 239000013307 optical fiber Substances 0.000 title claims description 84
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 229920000642 polymer Polymers 0.000 claims description 84
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 68
- 239000000178 monomer Substances 0.000 claims description 59
- 239000011248 coating agent Substances 0.000 claims description 52
- 238000000576 coating method Methods 0.000 claims description 52
- 239000002019 doping agent Substances 0.000 claims description 46
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 32
- JYNDMWZEMQAWTD-UHFFFAOYSA-N 2,2,2-trichloroethyl prop-2-enoate Chemical compound ClC(Cl)(Cl)COC(=O)C=C JYNDMWZEMQAWTD-UHFFFAOYSA-N 0.000 claims description 31
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 claims description 31
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 claims description 31
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 claims description 30
- 239000000470 constituent Substances 0.000 claims description 27
- -1 N-cHMI Chemical compound 0.000 claims description 23
- 238000001125 extrusion Methods 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 18
- 238000009826 distribution Methods 0.000 claims description 17
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 12
- 238000009792 diffusion process Methods 0.000 claims description 10
- 239000004417 polycarbonate Substances 0.000 claims description 8
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 claims description 8
- 229920003023 plastic Polymers 0.000 claims description 7
- 229920000515 polycarbonate Polymers 0.000 claims description 7
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- YBQZXXMEJHZYMB-UHFFFAOYSA-N 1,2-diphenylhydrazine Chemical compound C=1C=CC=CC=1NNC1=CC=CC=C1 YBQZXXMEJHZYMB-UHFFFAOYSA-N 0.000 claims description 5
- IUGNCEABJSRDPG-UHFFFAOYSA-N 2,2,2-trichloroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(Cl)(Cl)Cl IUGNCEABJSRDPG-UHFFFAOYSA-N 0.000 claims description 4
- BQTPKSBXMONSJI-UHFFFAOYSA-N 1-cyclohexylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1CCCCC1 BQTPKSBXMONSJI-UHFFFAOYSA-N 0.000 claims description 2
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- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 6
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- 238000009987 spinning Methods 0.000 description 5
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 4
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- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
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- 229910052736 halogen Inorganic materials 0.000 description 2
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- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 2
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- LVJZCPNIJXVIAT-UHFFFAOYSA-N 1-ethenyl-2,3,4,5,6-pentafluorobenzene Chemical compound FC1=C(F)C(F)=C(C=C)C(F)=C1F LVJZCPNIJXVIAT-UHFFFAOYSA-N 0.000 description 1
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- YEKDUBMGZZTUDY-UHFFFAOYSA-N 1-tert-butylpyrrole-2,5-dione Chemical compound CC(C)(C)N1C(=O)C=CC1=O YEKDUBMGZZTUDY-UHFFFAOYSA-N 0.000 description 1
- QTKPMCIBUROOGY-UHFFFAOYSA-N 2,2,2-trifluoroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)F QTKPMCIBUROOGY-UHFFFAOYSA-N 0.000 description 1
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- KQLLANJDGBFIAI-UHFFFAOYSA-N CC(C)OOCCCCC(C)O Chemical compound CC(C)OOCCCCC(C)O KQLLANJDGBFIAI-UHFFFAOYSA-N 0.000 description 1
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- 229920002647 polyamide Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- RHSWMKFUVRFEDV-UHFFFAOYSA-N tert-butyl 2-methyl-2-[[2-methyl-1-[(2-methylpropan-2-yl)oxy]-1-oxopropan-2-yl]diazenyl]propanoate Chemical compound CC(C)(C)OC(=O)C(C)(C)N=NC(C)(C)C(=O)OC(C)(C)C RHSWMKFUVRFEDV-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/045—Light guides
- G02B1/046—Light guides characterised by the core material
-
- 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
- C08F20/00—Homopolymers and copolymers 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
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
- C08F20/14—Methyl esters, e.g. methyl (meth)acrylate
-
- 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
- C08F20/00—Homopolymers and copolymers 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
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/22—Esters containing halogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
- C08L33/16—Homopolymers or copolymers of esters containing halogen atoms
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/045—Light guides
- G02B1/048—Light guides characterised by the cladding material
-
- 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
- C08F220/00—Copolymers 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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1806—C6-(meth)acrylate, e.g. (cyclo)hexyl (meth)acrylate or phenyl (meth)acrylate
-
- 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
- C08F220/00—Copolymers 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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1811—C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate
-
- 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
- C08F220/00—Copolymers 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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/22—Esters containing halogen
-
- 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
- C08F222/00—Copolymers 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
- C08F222/36—Amides or imides
- C08F222/40—Imides, e.g. cyclic imides
- C08F222/402—Alkyl substituted imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
-
- 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
- G02B6/02033—Core or cladding made from organic material, e.g. polymeric material
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009163317 | 2009-07-10 | ||
| JP2009293955 | 2009-12-25 | ||
| JP2010087570 | 2010-04-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201106031A TW201106031A (en) | 2011-02-16 |
| TWI471619B true TWI471619B (zh) | 2015-02-01 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW99122624A TWI471619B (zh) | 2009-07-10 | 2010-07-09 | Optical fiber and its manufacturing method |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8611714B2 (enExample) |
| EP (1) | EP2453270B1 (enExample) |
| JP (1) | JP5419815B2 (enExample) |
| KR (1) | KR20120061831A (enExample) |
| CN (1) | CN102472861B (enExample) |
| CA (1) | CA2767727A1 (enExample) |
| IN (1) | IN2012DN01200A (enExample) |
| TW (1) | TWI471619B (enExample) |
| WO (1) | WO2011004785A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102132185B (zh) * | 2008-06-23 | 2013-03-06 | 三菱丽阳株式会社 | 塑料光纤缆及信号传输方法 |
| CN102326106B (zh) * | 2009-02-20 | 2013-07-31 | 积水化学工业株式会社 | Gi型光纤及其制造方法 |
| JP5419815B2 (ja) * | 2009-07-10 | 2014-02-19 | 積水化学工業株式会社 | 光ファイバー及びその製造方法 |
| JP2012140559A (ja) * | 2011-01-06 | 2012-07-26 | Sekisui Chem Co Ltd | 樹脂組成物、成形体及び光ファイバー |
| PL3064970T3 (pl) * | 2013-11-01 | 2020-06-01 | Toray Industries, Inc. | Światłowód oświetlający z tworzywa sztucznego i sposób jego wytwarzania |
| CN105849610A (zh) * | 2013-12-11 | 2016-08-10 | 英派尔科技开发有限公司 | 光波导的制备和使用 |
| US10093787B2 (en) * | 2016-08-18 | 2018-10-09 | The Hong Kong Polytechnic University | Polymeric waveguide with single dopant |
| DK3764131T3 (da) * | 2018-03-05 | 2023-09-25 | Toray Industries | Optisk plastfiber og optisk plastfiberledning |
| TWI843720B (zh) | 2018-03-13 | 2024-06-01 | 小池康 | 一體成型多重光傳送片、一體成型多重光傳送片連接器及其製造方法 |
| EP3862800B1 (en) * | 2018-11-01 | 2023-11-22 | Kuraray Co., Ltd. | Light-emitting fiber |
| JP2020173390A (ja) * | 2019-04-12 | 2020-10-22 | 日東電工株式会社 | プラスチック光ファイバー及びその製造方法 |
| CN110670169B (zh) * | 2019-09-04 | 2022-03-15 | 苏州大学 | 一种聚合物光纤的制备方法 |
| EP4150385A1 (en) * | 2020-05-13 | 2023-03-22 | Haute Ecole Arc | Optical waveguide and method of fabrication thereof |
| US20240195503A1 (en) | 2021-04-07 | 2024-06-13 | Yasuhiro Koike | Optical transmission system, optical transmission path, and photoelectric composite cable |
| US12298553B2 (en) * | 2022-03-31 | 2025-05-13 | Microsoft Technology Licensing, Llc | Graded-index polymer optical fibre and the fabrication thereof |
| US20230314695A1 (en) * | 2022-03-31 | 2023-10-05 | Microsoft Technology Licensing, Llc | Multi-core optical fibre and fabrication thereof |
| US11931977B2 (en) | 2022-03-31 | 2024-03-19 | Microsoft Technology Licensing, Llc | Multi-core polymer optical fibre and the fabrication thereof |
| CN115840297A (zh) * | 2022-11-30 | 2023-03-24 | 安徽大学 | 基于聚合物光纤产生涡旋光的方法 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4756599A (en) * | 1986-09-09 | 1988-07-12 | Central Glass Company, Limited | Optical fiber using vinylidene fluoride base ternary copolymer as cladding material |
| JPH04243203A (ja) * | 1991-01-17 | 1992-08-31 | Showa Denko Kk | プラスチック光ファイバー |
| CN1283713A (zh) * | 1999-07-05 | 2001-02-14 | 阿尔卡塔尔公司 | 指数梯度塑料光学纤维的制备方法 |
| JP2003139972A (ja) * | 2001-11-02 | 2003-05-14 | Mitsubishi Rayon Co Ltd | プラスチック光ファイバ、プラスチック光ファイバケーブル及びプラグ付きプラスチック光ファイバケーブル |
| TW200702760A (en) * | 2005-05-16 | 2007-01-16 | 3M Innovative Properties Co | Lateral emitting optical fiber and light emitting device |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62156105A (ja) * | 1985-06-20 | 1987-07-11 | Mitsubishi Rayon Co Ltd | メタクリルイミド含有重合体 |
| JPH0644085B2 (ja) | 1985-12-20 | 1994-06-08 | 住友電気工業株式会社 | プラスチツク光フアイバおよびその製法 |
| JPH0814646B2 (ja) * | 1986-12-15 | 1996-02-14 | 旭化成工業株式会社 | 耐熱性プラスチツク光フアイバ− |
| KR0170358B1 (ko) | 1991-10-22 | 1999-05-01 | . | 굴절률 분포형 광학 수지 재료와 그 제조 방법 및 광전송체 |
| JPH11337781A (ja) * | 1998-05-29 | 1999-12-10 | Asahi Glass Co Ltd | 被覆プラスチック光ファイバおよびその製造方法 |
| JP2001116967A (ja) * | 1999-08-06 | 2001-04-27 | Shin Etsu Chem Co Ltd | 光ファイバテープ及びその製造方法 |
| GB0013767D0 (en) * | 2000-06-07 | 2000-07-26 | Univ Heriot Watt | Photo-polymers and use thereof |
| JP2003226558A (ja) * | 2002-02-05 | 2003-08-12 | Shin Etsu Chem Co Ltd | 光ファイバ被覆用電子線硬化型樹脂組成物及び光ファイバ心線 |
| KR20040088402A (ko) * | 2003-04-01 | 2004-10-16 | 후지 샤신 필름 가부시기가이샤 | 플라스틱 광섬유 제조 방법 및 장치 |
| JP2005035284A (ja) * | 2003-06-30 | 2005-02-10 | Sekisui Chem Co Ltd | 屈折率分布型光学材料の製造方法 |
| JP4243203B2 (ja) | 2004-01-21 | 2009-03-25 | 積水ハウス株式会社 | 階段の接続構造 |
| JP2006010775A (ja) * | 2004-06-22 | 2006-01-12 | Fuji Photo Film Co Ltd | プラスチック光ファイバプリフォームの製造方法 |
| JP2006208551A (ja) * | 2005-01-26 | 2006-08-10 | Fuji Photo Film Co Ltd | プラスチック光ファイバ素線の製造方法およびその製造設備 |
| KR101016082B1 (ko) * | 2005-05-09 | 2011-02-17 | 미츠비시 레이온 가부시키가이샤 | 플라스틱 광섬유 케이블 |
| JP2007163910A (ja) * | 2005-12-15 | 2007-06-28 | Fujifilm Corp | プラスチック光ファイバ素線およびその製造方法 |
| JP2008250112A (ja) * | 2007-03-30 | 2008-10-16 | Sekisui Chem Co Ltd | プラスチック製光伝送体及びポリ塩化ビニル系樹脂製光伝送体の製造方法 |
| CN102132185B (zh) * | 2008-06-23 | 2013-03-06 | 三菱丽阳株式会社 | 塑料光纤缆及信号传输方法 |
| CN102326106B (zh) * | 2009-02-20 | 2013-07-31 | 积水化学工业株式会社 | Gi型光纤及其制造方法 |
| JP5419815B2 (ja) * | 2009-07-10 | 2014-02-19 | 積水化学工業株式会社 | 光ファイバー及びその製造方法 |
-
2010
- 2010-07-05 JP JP2010152733A patent/JP5419815B2/ja active Active
- 2010-07-05 KR KR1020127003520A patent/KR20120061831A/ko not_active Ceased
- 2010-07-05 CN CN2010800309547A patent/CN102472861B/zh active Active
- 2010-07-05 WO PCT/JP2010/061378 patent/WO2011004785A1/ja not_active Ceased
- 2010-07-05 EP EP10797096.4A patent/EP2453270B1/en not_active Not-in-force
- 2010-07-05 CA CA2767727A patent/CA2767727A1/en not_active Abandoned
- 2010-07-05 US US13/383,041 patent/US8611714B2/en not_active Expired - Fee Related
- 2010-07-09 TW TW99122624A patent/TWI471619B/zh active
- 2010-07-10 IN IN1200DEN2012 patent/IN2012DN01200A/en unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4756599A (en) * | 1986-09-09 | 1988-07-12 | Central Glass Company, Limited | Optical fiber using vinylidene fluoride base ternary copolymer as cladding material |
| JPH04243203A (ja) * | 1991-01-17 | 1992-08-31 | Showa Denko Kk | プラスチック光ファイバー |
| CN1283713A (zh) * | 1999-07-05 | 2001-02-14 | 阿尔卡塔尔公司 | 指数梯度塑料光学纤维的制备方法 |
| JP2003139972A (ja) * | 2001-11-02 | 2003-05-14 | Mitsubishi Rayon Co Ltd | プラスチック光ファイバ、プラスチック光ファイバケーブル及びプラグ付きプラスチック光ファイバケーブル |
| TW200702760A (en) * | 2005-05-16 | 2007-01-16 | 3M Innovative Properties Co | Lateral emitting optical fiber and light emitting device |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2453270A4 (en) | 2015-05-13 |
| CN102472861B (zh) | 2013-06-26 |
| WO2011004785A1 (ja) | 2011-01-13 |
| EP2453270A1 (en) | 2012-05-16 |
| US20120114291A1 (en) | 2012-05-10 |
| US8611714B2 (en) | 2013-12-17 |
| IN2012DN01200A (enExample) | 2015-04-10 |
| CA2767727A1 (en) | 2011-01-13 |
| TW201106031A (en) | 2011-02-16 |
| EP2453270B1 (en) | 2016-06-22 |
| JP5419815B2 (ja) | 2014-02-19 |
| JP2011232726A (ja) | 2011-11-17 |
| KR20120061831A (ko) | 2012-06-13 |
| CN102472861A (zh) | 2012-05-23 |
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