KR100965682B1 - 경사 구조를 가진 광학 요소의 생산 방법 - Google Patents
경사 구조를 가진 광학 요소의 생산 방법 Download PDFInfo
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- KR100965682B1 KR100965682B1 KR1020047010728A KR20047010728A KR100965682B1 KR 100965682 B1 KR100965682 B1 KR 100965682B1 KR 1020047010728 A KR1020047010728 A KR 1020047010728A KR 20047010728 A KR20047010728 A KR 20047010728A KR 100965682 B1 KR100965682 B1 KR 100965682B1
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- nanoscale particles
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- hydrolyzable
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- XPGAWFIWCWKDDL-UHFFFAOYSA-N propan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCC[O-].CCC[O-].CCC[O-].CCC[O-] XPGAWFIWCWKDDL-UHFFFAOYSA-N 0.000 description 1
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- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
-
- 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
- G02B6/10—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type
- G02B6/12—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings of the optical waveguide type of the integrated circuit kind
- G02B6/13—Integrated optical circuits characterised by the manufacturing method
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
- C08F283/124—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes on to polysiloxanes having carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
- C08L51/085—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds on to polysiloxanes
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B3/00—Simple or compound lenses
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B3/00—Simple or compound lenses
- G02B3/0087—Simple or compound lenses with index gradient
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31507—Of polycarbonate
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Polymerisation Methods In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Holo Graphy (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10200648A DE10200648A1 (de) | 2002-01-10 | 2002-01-10 | Verfahren zur Herstellung Optischer Elemente mit Gradientenstruktur |
| DE10200648.2 | 2002-01-10 | ||
| PCT/EP2003/000193 WO2003058292A1 (de) | 2002-01-10 | 2003-01-10 | Verfahren zur herstellung optischer elemente mit gradientenstruktur |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20040072713A KR20040072713A (ko) | 2004-08-18 |
| KR100965682B1 true KR100965682B1 (ko) | 2010-06-24 |
Family
ID=7711807
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020047010728A Expired - Lifetime KR100965682B1 (ko) | 2002-01-10 | 2003-01-10 | 경사 구조를 가진 광학 요소의 생산 방법 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7390532B2 (OSRAM) |
| EP (1) | EP1463963B1 (OSRAM) |
| JP (1) | JP4419167B2 (OSRAM) |
| KR (1) | KR100965682B1 (OSRAM) |
| DE (1) | DE10200648A1 (OSRAM) |
| TW (1) | TWI268364B (OSRAM) |
| WO (1) | WO2003058292A1 (OSRAM) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005101067A1 (ja) * | 2004-04-13 | 2005-10-27 | Matsushita Electric Industrial Co., Ltd. | 集光素子および固体撮像装置 |
| US7653278B2 (en) * | 2004-05-21 | 2010-01-26 | Panasonic Corporation | Refractive index distribution type optical member, and production method for refractive index distribution type optical member |
| TWI393226B (zh) * | 2004-11-04 | 2013-04-11 | 台灣積體電路製造股份有限公司 | 基於奈米管之填充物 |
| US7400809B2 (en) | 2004-12-10 | 2008-07-15 | General Electric Company | Optical waveguide devices and method of making the same |
| DE102004061323A1 (de) | 2004-12-20 | 2006-06-22 | Epg (Engineered Nanoproducts Germany)Gmbh | Optische Komponente aus einem anorganisch-organischen Hybridmaterial zur Herstellung von Brechzahlgradientenschichten mit hoher lateraler Auflösung und Verfahren zu ihrer Herstellung |
| DE102004061324A1 (de) | 2004-12-20 | 2006-06-22 | Epg (Engineered Nanoproducts Germany)Gmbh | Optische Komponente aus einem anorganisch-organischen Hybridmaterial zur Herstellung von Brechzahlgradientenschichten mit schneller Kinetik und Verfahren zu ihrer Herstellung |
| JP4470854B2 (ja) * | 2005-10-17 | 2010-06-02 | ソニー株式会社 | 通信方法および通信システム |
| DE102005050593A1 (de) * | 2005-10-21 | 2007-04-26 | Esk Ceramics Gmbh & Co. Kg | Dauerhafte siliciumnitridhaltige Hartbeschichtung |
| US20070179239A1 (en) * | 2006-01-30 | 2007-08-02 | Matsushita Electric Industrial Co., Ltd. | Dynamic optical components based on thermochromic materials |
| DE102006011949A1 (de) | 2006-03-15 | 2007-09-20 | Epg (Engineered Nanoproducts Germany) Ag | Verfahren zur Herstellung von defektfreien mikrooptischen Lichtlenkelementen grosser Breite |
| JP5188045B2 (ja) * | 2006-08-30 | 2013-04-24 | キヤノン株式会社 | ナノ酸化物粒子及びその製造方法 |
| US8322754B2 (en) | 2006-12-01 | 2012-12-04 | Tenaris Connections Limited | Nanocomposite coatings for threaded connections |
| WO2008098069A1 (en) * | 2007-02-06 | 2008-08-14 | Nanodynamics, Inc. | Directed migration of hydrophobic nanomaterials at surfaces |
| CA2682965A1 (en) * | 2007-04-05 | 2008-12-24 | Polytechnic University | Improvements in nanocomposites and their surfaces |
| DE102007017032B4 (de) * | 2007-04-11 | 2011-09-22 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Verfahren zur Herstellung von flächigen Größen- oder Abstandsvariationen in Mustern von Nanostrukturen auf Oberflächen |
| JP5115125B2 (ja) * | 2007-10-05 | 2013-01-09 | Ｔｄｋ株式会社 | ホログラム記録材料及びホログラム記録媒体 |
| DE102007053284A1 (de) * | 2007-11-08 | 2009-05-20 | Esk Ceramics Gmbh & Co. Kg | Fest haftende siliciumnitridhaltige Trennschicht |
| US20100302487A1 (en) * | 2007-12-28 | 2010-12-02 | Storer Joey W | Phase compensation film |
| US20100294989A1 (en) * | 2007-12-28 | 2010-11-25 | Shaffer Ii Edward O | Small scale functional materials |
| DE102008009332A1 (de) | 2008-02-14 | 2009-08-20 | Leibniz-Institut Für Neue Materialien Gemeinnützige Gmbh | Optische Elemente mit Gradientenstruktur |
| FR2938679B1 (fr) * | 2008-11-20 | 2011-04-29 | Univ Jean Monnet | Procede de texturation aleatoire reconfigurable d'un element photochromique et procede de securisation et/ou authentification mettant en oeuvre ce procede |
| DE102008064168A1 (de) | 2008-12-22 | 2010-06-24 | Leibniz-Institut Für Neue Materialien Gemeinnützige Gmbh | Verfahren und Zusammensetzung zur Herstellung optischer Elemente mit Gradientenstruktur |
| US20110032587A1 (en) * | 2009-03-20 | 2011-02-10 | Absolute Imaging LLC | System and Method for Autostereoscopic Imaging |
| US20110058240A1 (en) | 2009-03-20 | 2011-03-10 | Absolute Imaging LLC | System and Method for Autostereoscopic Imaging Using Holographic Optical Element |
| JP2011227466A (ja) * | 2010-04-02 | 2011-11-10 | Canon Inc | レンズ及びレンズの製造方法 |
| US8586173B2 (en) * | 2010-06-30 | 2013-11-19 | Sigma Laboratories Of Arizona, Llc | Nano-structured dielectric composite |
| SE535087C2 (sv) | 2010-08-24 | 2012-04-10 | En metod för att preparera en plan yta med en kontrollerad täthetsgradient av deponerade partiklar i nanostorlek | |
| US8368106B2 (en) * | 2010-11-04 | 2013-02-05 | Industrial Technology Research Institute | Gradient composite material and method of manufacturing the same |
| EP2649126A4 (en) * | 2010-12-09 | 2015-10-21 | Kilolambda Tech Ltd | QUICK RESPONSE PHOTOCHROME COMPOSITION AND DEVICE THEREFOR |
| KR101961115B1 (ko) * | 2012-02-07 | 2019-03-26 | 삼성전자주식회사 | 성형품, 이의 제조 방법 및 상기 성형품을 포함하는 디스플레이 장치 |
| CN102866439A (zh) * | 2012-09-21 | 2013-01-09 | 蚌埠玻璃工业设计研究院 | 一种基于高分子聚合物的cpv技术用梯度折射率透镜及其制备方法 |
| US9765178B2 (en) | 2013-06-19 | 2017-09-19 | Empire Technology Development Llc | Self-writing waveguide with nanoparticles |
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| US9575250B2 (en) * | 2014-07-03 | 2017-02-21 | Empire Technology Development Llc | Direct writable and erasable waveguides in optoelectronic systems |
| JP6782295B2 (ja) * | 2015-10-05 | 2020-11-11 | シャンハイ ナーグアン インフォメーション テクノロジー コーポレイションＳｈａｎｇｈａｉ Ｎａｇｕａｎｇ Ｉｎｆｏｒｍａｔｉｏｎ Ｔｅｃｈｎｏｌｏｇｙ Ｃｏｒｐｏｒａｔｉｏｎ | 光学データ記憶用の媒体、システム、及び方法 |
| EP3375827A1 (de) * | 2017-03-17 | 2018-09-19 | TIGER Coatings GmbH & Co. KG | Laminat-tinte |
| CN108274738B (zh) * | 2018-01-24 | 2020-03-17 | 青岛理工大学 | 一种多尺度可见光波段梯度折射率透镜的制备方法 |
| EP3768438A4 (en) * | 2018-03-21 | 2022-03-23 | Bar Ilan University | THIN IN-SITU COATING OF OXIDE PARTICLES ON SURFACES AND RELATED APPLICATIONS |
| KR102338107B1 (ko) | 2018-09-14 | 2021-12-09 | 주식회사 엘지화학 | 홀로그램 매체 |
| EP3643765A1 (en) * | 2018-10-22 | 2020-04-29 | SABIC Global Technologies B.V. | Stable quantum dot compositions |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6236493B1 (en) * | 1996-04-04 | 2001-05-22 | Institut für Neue Materialien Gemeinnützige GmbH | Optical components with a graded-index structure, and method of manufacturing such components |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5360834A (en) * | 1989-08-01 | 1994-11-01 | Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. | Process for photoinitiated control of inorganic network formation in the sol-gel process |
| DE3925462A1 (de) * | 1989-08-01 | 1991-02-07 | Fraunhofer Ges Forschung | Verfahren zur photoinitiierten steuerung der anorganischen netzwerkbildung beim sol-gel-prozess |
| US5158858A (en) * | 1990-07-05 | 1992-10-27 | E. I. Du Pont De Nemours And Company | Solid imaging system using differential tension elastomeric film |
| DE4133621A1 (de) * | 1991-10-10 | 1993-04-22 | Inst Neue Mat Gemein Gmbh | Nanoskalige teilchen enthaltende kompositmaterialien, verfahren zu deren herstellung und deren verwendung fuer optische elemente |
| DE4212633A1 (de) | 1992-04-15 | 1993-10-21 | Inst Neue Mat Gemein Gmbh | Verfahren zur Herstellung oberflächenmodifizierter nanoskaliger keramischer Pulver |
| DE4232188C2 (de) * | 1992-09-25 | 1995-05-18 | Du Pont Deutschland | Wiederverwertung der Aufzeichnungsschicht von Flexodruckplatten |
| DE19524859A1 (de) * | 1995-07-07 | 1997-01-09 | Fraunhofer Ges Forschung | Metallalkoxide mit hydrolysestabiler Komplexbindung von Anionen der Hydroxamsäure |
| DE19719948A1 (de) | 1997-05-13 | 1998-11-19 | Inst Neue Mat Gemein Gmbh | Nanostrukturierte Formkörper und Schichten sowie Verfahren zu deren Herstellung |
| MY122234A (en) * | 1997-05-13 | 2006-04-29 | Inst Neue Mat Gemein Gmbh | Nanostructured moulded bodies and layers and method for producing same |
| DE19746885A1 (de) | 1997-10-23 | 1999-06-24 | Inst Neue Mat Gemein Gmbh | Nanostrukturierte Formkörper und Schichten sowie Verfahren zu deren Herstellung |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US6236493B1 (en) * | 1996-04-04 | 2001-05-22 | Institut für Neue Materialien Gemeinnützige GmbH | Optical components with a graded-index structure, and method of manufacturing such components |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20040072713A (ko) | 2004-08-18 |
| JP2005514645A (ja) | 2005-05-19 |
| US7390532B2 (en) | 2008-06-24 |
| EP1463963B1 (de) | 2014-03-12 |
| WO2003058292A1 (de) | 2003-07-17 |
| EP1463963A1 (de) | 2004-10-06 |
| JP4419167B2 (ja) | 2010-02-24 |
| TW200301827A (en) | 2003-07-16 |
| DE10200648A1 (de) | 2003-07-24 |
| TWI268364B (en) | 2006-12-11 |
| US20050059760A1 (en) | 2005-03-17 |
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