DE60007753T2 - Verfahren zum verbinden einer photochromen beschichtung an ein polymeres substrat - Google Patents
Verfahren zum verbinden einer photochromen beschichtung an ein polymeres substrat Download PDFInfo
- Publication number
- DE60007753T2 DE60007753T2 DE60007753T DE60007753T DE60007753T2 DE 60007753 T2 DE60007753 T2 DE 60007753T2 DE 60007753 T DE60007753 T DE 60007753T DE 60007753 T DE60007753 T DE 60007753T DE 60007753 T2 DE60007753 T2 DE 60007753T2
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- Prior art keywords
- photochromic
- composition
- organic
- radicals
- polymer
- Prior art date
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- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 description 1
- UZIAQVMNAXPCJQ-UHFFFAOYSA-N triethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)COC(=O)C(C)=C UZIAQVMNAXPCJQ-UHFFFAOYSA-N 0.000 description 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- UOKUUKOEIMCYAI-UHFFFAOYSA-N trimethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)COC(=O)C(C)=C UOKUUKOEIMCYAI-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- C09D4/00—Coating 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/05—Bonding or intermediate layer characterised by chemical composition, e.g. sealant or spacer
- C09K2323/053—Organic silicon compound, e.g. organosilicon
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S348/00—Television
- Y10S348/902—Photochromic
-
- 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]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/348,135 US6150430A (en) | 1999-07-06 | 1999-07-06 | Process for adhering a photochromic coating to a polymeric substrate |
| US348135 | 1999-07-06 | ||
| PCT/US2000/018575 WO2001002472A1 (en) | 1999-07-06 | 2000-07-06 | Process for adhering a photochromic coating to a polymeric substrate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60007753D1 DE60007753D1 (de) | 2004-02-19 |
| DE60007753T2 true DE60007753T2 (de) | 2004-11-11 |
Family
ID=23366785
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60007753T Expired - Lifetime DE60007753T2 (de) | 1999-07-06 | 2000-07-06 | Verfahren zum verbinden einer photochromen beschichtung an ein polymeres substrat |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6150430A (enExample) |
| EP (1) | EP1200512B1 (enExample) |
| JP (1) | JP4638639B2 (enExample) |
| AU (1) | AU754726B2 (enExample) |
| BR (1) | BR0012208B1 (enExample) |
| DE (1) | DE60007753T2 (enExample) |
| WO (1) | WO2001002472A1 (enExample) |
Families Citing this family (127)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU769249B2 (en) | 1999-07-02 | 2004-01-22 | Ppg Industries Ohio, Inc. | Poly(meth)acrylic photochromic coating |
| CZ20021370A3 (cs) * | 1999-10-28 | 2002-10-16 | Daicel Chemical Industries, Ltd. | Spouątěč elektrického typu a vyvíječ plynu |
| US6531076B2 (en) | 2000-02-04 | 2003-03-11 | Ppg Industries Ohio, Inc. | Photochromic organic resin composition |
| WO2001057106A1 (en) * | 2000-02-04 | 2001-08-09 | Ppg Industries Ohio, Inc. | Photochromic coated articles |
| FR2806076B1 (fr) * | 2000-03-08 | 2002-09-20 | Saint Gobain Vitrage | Substrat transparent revetu d'une couche polymere |
| US7077985B2 (en) | 2000-05-30 | 2006-07-18 | Vision-Ease Lens | Injection molding of lens |
| JP3922873B2 (ja) * | 2000-09-29 | 2007-05-30 | 株式会社トクヤマ | 硬化性組成物 |
| KR100652041B1 (ko) * | 2000-12-29 | 2006-11-30 | 엘지.필립스 엘시디 주식회사 | 액정표시소자 및 그 제조방법 |
| US6773108B2 (en) * | 2001-03-21 | 2004-08-10 | Invicta Corporation | Lens with photochromic elastomer film and method of making it |
| US6998072B2 (en) * | 2001-11-01 | 2006-02-14 | Transitions Optical, Inc. | Photochromic polymerizable compositions |
| US6916537B2 (en) * | 2001-11-01 | 2005-07-12 | Transitions Optical Inc. | Articles having a photochromic polymeric coating |
| US8017720B2 (en) | 2005-12-16 | 2011-09-13 | Ppg Industries Ohio, Inc. | Sulfur-containing oligomers and high index polyurethanes prepared therefrom |
| US7452611B2 (en) * | 2001-12-27 | 2008-11-18 | Transitions Optical, Inc. | Photochromic optical article |
| US7410691B2 (en) * | 2001-12-27 | 2008-08-12 | Ppg Industries Ohio, Inc. | Photochromic optical article |
| DE10202565A1 (de) * | 2002-01-24 | 2003-08-07 | Basf Coatings Ag | Gehärtete Materialien, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US7036932B2 (en) * | 2002-10-04 | 2006-05-02 | Vision-Ease Lens | Laminated functional wafer for plastic optical elements |
| US20040071978A1 (en) * | 2002-10-15 | 2004-04-15 | Omnova Solutions Inc. | Laminate and method of production |
| US7009032B2 (en) | 2002-12-20 | 2006-03-07 | Ppg Industries Ohio, Inc. | Sulfide-containing polythiols |
| US7166357B2 (en) * | 2003-03-20 | 2007-01-23 | Transitions Optical, Inc. | Photochromic articles that activate behind ultraviolet radiation blocking transparencies and methods for preparation |
| US7320826B2 (en) * | 2003-03-20 | 2008-01-22 | Ppg Industries Ohio, Inc. | Photochromic articles with reduced temperature dependency and methods for preparation |
| US20040186241A1 (en) * | 2003-03-20 | 2004-09-23 | Gemert Barry Van | Photochromic ocular devices |
| US7262295B2 (en) | 2003-03-20 | 2007-08-28 | Transitions Optical, Inc. | Indeno-fused photochromic naphthopyrans, naphthols and photochromic articles |
| US7128415B2 (en) * | 2003-04-30 | 2006-10-31 | Polylite Taiwan Company, Ltd | Method of forming polarized or photochromic lenses by fusing polycarbonate with other plastic materials |
| US8582192B2 (en) | 2003-07-01 | 2013-11-12 | Transitions Optical, Inc. | Polarizing photochromic articles |
| US8211338B2 (en) | 2003-07-01 | 2012-07-03 | Transitions Optical, Inc | Photochromic compounds |
| WO2005006034A2 (en) | 2003-07-01 | 2005-01-20 | Transitions Optical, Inc. | Alignment facilities for optical dyes |
| US7256921B2 (en) | 2003-07-01 | 2007-08-14 | Transitions Optical, Inc. | Polarizing, photochromic devices and methods of making the same |
| US7632540B2 (en) | 2003-07-01 | 2009-12-15 | Transitions Optical, Inc. | Alignment facilities for optical dyes |
| US7342112B2 (en) | 2003-07-01 | 2008-03-11 | Ppg Industries Ohio, Inc. | Photochromic compounds |
| US8545015B2 (en) | 2003-07-01 | 2013-10-01 | Transitions Optical, Inc. | Polarizing photochromic articles |
| US8518546B2 (en) | 2003-07-01 | 2013-08-27 | Transitions Optical, Inc. | Photochromic compounds and compositions |
| US9096014B2 (en) | 2003-07-01 | 2015-08-04 | Transitions Optical, Inc. | Oriented polymeric sheets exhibiting dichroism and articles containing the same |
| US7978391B2 (en) | 2004-05-17 | 2011-07-12 | Transitions Optical, Inc. | Polarizing, photochromic devices and methods of making the same |
| US8089678B2 (en) | 2003-07-01 | 2012-01-03 | Transitions Optical, Inc | Clear to circular polarizing photochromic devices and methods of making the same |
| US8698117B2 (en) | 2003-07-01 | 2014-04-15 | Transitions Optical, Inc. | Indeno-fused ring compounds |
| US8545984B2 (en) | 2003-07-01 | 2013-10-01 | Transitions Optical, Inc. | Photochromic compounds and compositions |
| US6984262B2 (en) * | 2003-07-16 | 2006-01-10 | Transitions Optical, Inc. | Adhesion enhancing coating composition, process for using and articles produced |
| AU2004270746B2 (en) | 2003-09-09 | 2010-12-02 | Insight Equity A.P.X., Lp | Photochromic polyurethane laminate |
| US7858001B2 (en) | 2003-09-09 | 2010-12-28 | Insight Equity A.P.X., L.P. | Photochromic lens |
| US7488510B2 (en) * | 2003-10-28 | 2009-02-10 | Signet Armorlite, Inc. | Compositions and methods for the preparation of composite photochromic polycarbonate lenses |
| US7094368B2 (en) * | 2003-12-10 | 2006-08-22 | Transitions Optical, Inc. | Pyrano-quinolines, pyrano-quinolinones, combinations thereof, photochromic compositions and articles |
| US7097303B2 (en) | 2004-01-14 | 2006-08-29 | Ppg Industries Ohio, Inc. | Polarizing devices and methods of making the same |
| US20050196626A1 (en) * | 2004-03-04 | 2005-09-08 | Knox Carol L. | Photochromic optical article |
| US20050196616A1 (en) * | 2004-03-04 | 2005-09-08 | Stewart Kevin J. | Photochromic optical article |
| US7261843B2 (en) | 2004-03-04 | 2007-08-28 | Transitions Optical, Inc. | Photochromic optical article |
| US7189456B2 (en) | 2004-03-04 | 2007-03-13 | Transitions Optical, Inc. | Photochromic optical article |
| US7144966B2 (en) * | 2004-03-04 | 2006-12-05 | Basf Corporation | Acrylic composition for use in coating applications and a method of forming the same |
| US7811480B2 (en) * | 2004-03-04 | 2010-10-12 | Transitions Optical, Inc. | Photochromic optical article |
| US8563212B2 (en) * | 2004-07-16 | 2013-10-22 | Transitions Optical, Inc. | Methods for producing photosensitive microparticles, non-aqueous dispersions thereof and articles prepared therewith |
| US8153344B2 (en) * | 2004-07-16 | 2012-04-10 | Ppg Industries Ohio, Inc. | Methods for producing photosensitive microparticles, aqueous compositions thereof and articles prepared therewith |
| US8563213B2 (en) | 2004-07-16 | 2013-10-22 | Transitions Optical, Inc. | Methods for producing photosensitive microparticles |
| US9598527B2 (en) | 2004-09-01 | 2017-03-21 | Ppg Industries Ohio, Inc. | Polyurethanes, articles and coatings prepared therefrom and methods of making the same |
| US9464169B2 (en) | 2004-09-01 | 2016-10-11 | Ppg Industries Ohio, Inc. | Polyurethanes, articles and coatings prepared therefrom and methods of making the same |
| US11008418B2 (en) | 2004-09-01 | 2021-05-18 | Ppg Industries Ohio, Inc. | Polyurethanes, articles and coatings prepared therefrom and methods of making the same |
| US20090280709A1 (en) | 2004-09-01 | 2009-11-12 | Ppg Industries Ohio, Inc. | Polyurethanes, Articles and Coatings Prepared Therefrom and Methods of Making the Same |
| US11591436B2 (en) | 2004-09-01 | 2023-02-28 | Ppg Industries Ohio, Inc. | Polyurethane article and methods of making the same |
| US20090280329A1 (en) | 2004-09-01 | 2009-11-12 | Ppg Industries Ohio, Inc. | Polyurethanes, Articles and Coatings Prepared Therefrom and Methods of Making the Same |
| US11248083B2 (en) | 2004-09-01 | 2022-02-15 | Ppg Industries Ohio, Inc. | Aircraft windows |
| US11149107B2 (en) | 2004-09-01 | 2021-10-19 | Ppg Industries Ohio, Inc. | Polyurethanes, articles and coatings prepared therefrom and methods of making the same |
| KR100733920B1 (ko) * | 2004-09-17 | 2007-07-02 | 주식회사 엘지화학 | 에칭 레지스트용 잉크 조성물, 이를 이용한 에칭 레지스트패턴 형성 방법 및 미세 유로 형성 방법 |
| WO2006094313A2 (en) | 2005-03-04 | 2006-09-08 | Vision-Ease Lens | Forming method for polymeric laminated wafers comprising different film materials |
| US8647538B2 (en) | 2005-04-08 | 2014-02-11 | Transitions Optical, Inc. | Photochromic compounds having at least two photochromic moieties |
| US20060226402A1 (en) * | 2005-04-08 | 2006-10-12 | Beon-Kyu Kim | Ophthalmic devices comprising photochromic materials having extended PI-conjugated systems |
| US9139552B2 (en) | 2005-04-08 | 2015-09-22 | Transitions Optical, Inc. | Indeno-fused naphthopyrans having ethylenically unsaturated groups |
| US9052438B2 (en) * | 2005-04-08 | 2015-06-09 | Johnson & Johnson Vision Care, Inc. | Ophthalmic devices comprising photochromic materials with reactive substituents |
| US9028728B2 (en) | 2005-04-08 | 2015-05-12 | Transitions Optical, Inc. | Photochromic materials that include indeno-fused naphthopyrans |
| US8147725B2 (en) | 2005-04-08 | 2012-04-03 | Transitions Optical, Inc | Photochromic materials having extended pi-conjugated systems and compositions and articles including the same |
| US7556750B2 (en) * | 2005-04-08 | 2009-07-07 | Transitions Optical, Inc. | Photochromic materials with reactive substituents |
| US8158037B2 (en) | 2005-04-08 | 2012-04-17 | Johnson & Johnson Vision Care, Inc. | Photochromic materials having extended pi-conjugated systems and compositions and articles including the same |
| US20060228557A1 (en) * | 2005-04-08 | 2006-10-12 | Beon-Kyu Kim | Photochromic materials having extended pi-conjugated systems and compositions and articles including the same |
| US20060227287A1 (en) * | 2005-04-08 | 2006-10-12 | Frank Molock | Photochromic ophthalmic devices made with dual initiator system |
| DE102005029360B4 (de) * | 2005-06-24 | 2011-11-10 | Softal Corona & Plasma Gmbh | Zwei Verfahren zur kontinuierlichen Atmosphärendruck Plasmabehandlung von Werkstücken, insbesondere Materialplatten oder -bahnen |
| JP5021194B2 (ja) * | 2005-09-15 | 2012-09-05 | Hoya株式会社 | 硬化性組成物及びそれを用いた光学部材 |
| ES2339485T3 (es) * | 2005-12-14 | 2010-05-20 | The Procter And Gamble Company | Composiciones detergentes que contienen compuestos iniciadores de tipo azo para una capacidad de blanqueo mejorada y ventajas de eliminacion de manchas. |
| US7556751B2 (en) * | 2005-12-21 | 2009-07-07 | Transitions Optical, Inc. | Photochromic materials having electron-withdrawing substituents |
| US7527754B2 (en) * | 2005-12-21 | 2009-05-05 | Transitions Optical, Inc. | Photochromic indeno-fused naphthopyrans |
| US7687597B2 (en) | 2006-05-05 | 2010-03-30 | Ppg Industries Ohio, Inc. | Thioether functional oligomeric polythiols and articles prepared therefrom |
| US7481955B2 (en) * | 2006-05-31 | 2009-01-27 | Transitions Optical, Inc. | Photochromic materials comprising metallocenyl groups |
| US20070278461A1 (en) * | 2006-05-31 | 2007-12-06 | Transitions Optical, Inc. | Photochromic materials comprising haloalkyl groups |
| US20080107564A1 (en) | 2006-07-20 | 2008-05-08 | Shmuel Sternberg | Medical fluid access site with antiseptic indicator |
| US8748634B2 (en) * | 2006-10-30 | 2014-06-10 | Transitions Optical, Inc. | Photochromic materials demonstrating improved fade rates |
| US7906214B2 (en) | 2007-01-26 | 2011-03-15 | Transitions Optical, Inc. | Optical elements comprising compatiblizing coatings and methods of making the same |
| US7907346B2 (en) | 2007-03-16 | 2011-03-15 | Transitions Optical, Inc. | Photochromic materials and photochromic compositions and articles including the same |
| JP5118389B2 (ja) * | 2007-05-26 | 2013-01-16 | 中村製作所株式会社 | ワークへの凹所形成方法 |
| USRE47452E1 (en) | 2007-07-20 | 2019-06-25 | Baxter International Inc. | Antimicrobial housing and cover for a medical device |
| US9125973B2 (en) | 2007-07-20 | 2015-09-08 | Baxter International Inc. | Antimicrobial housing and cover for a medical device |
| JP2011508064A (ja) * | 2007-12-27 | 2011-03-10 | バクスター・インターナショナル・インコーポレイテッド | 照射硬化性コーティング |
| US8753561B2 (en) | 2008-06-20 | 2014-06-17 | Baxter International Inc. | Methods for processing substrates comprising metallic nanoparticles |
| US8178120B2 (en) | 2008-06-20 | 2012-05-15 | Baxter International Inc. | Methods for processing substrates having an antimicrobial coating |
| US20090326186A1 (en) * | 2008-06-27 | 2009-12-31 | Transitions Optical, Inc. | Mesogen containing compounds |
| US20100014010A1 (en) * | 2008-06-27 | 2010-01-21 | Transitions Optical, Inc. | Formulations comprising mesogen containing compounds |
| US8277826B2 (en) | 2008-06-25 | 2012-10-02 | Baxter International Inc. | Methods for making antimicrobial resins |
| US8431039B2 (en) | 2008-06-27 | 2013-04-30 | Transitions Optical, Inc. | Mesogenic stabilizers |
| US8349210B2 (en) | 2008-06-27 | 2013-01-08 | Transitions Optical, Inc. | Mesogenic stabilizers |
| US7910019B2 (en) | 2008-06-27 | 2011-03-22 | Transitions Optical, Inc. | Mesogen containing compounds |
| US8628685B2 (en) * | 2008-06-27 | 2014-01-14 | Transitions Optical, Inc | Mesogen-containing compounds |
| US8613868B2 (en) | 2008-06-27 | 2013-12-24 | Transitions Optical, Inc | Mesogenic stabilizers |
| US8623238B2 (en) | 2008-06-27 | 2014-01-07 | Transitions Optical, Inc. | Mesogenic stabilizers |
| US7910020B2 (en) * | 2008-06-27 | 2011-03-22 | Transitions Optical, Inc. | Liquid crystal compositions comprising mesogen containing compounds |
| US8084133B2 (en) * | 2008-08-06 | 2011-12-27 | Ppg Industries Ohio, Inc | Tintable film-forming compositions having high refractive indices and coated optical articles using same |
| US7911676B2 (en) * | 2008-12-16 | 2011-03-22 | Transitions Optical, Inc. | Photochromic optical articles prepared with reversible thermochromic materials |
| US20100232003A1 (en) | 2009-03-13 | 2010-09-16 | Transitions Optical, Inc. | Vision enhancing optical articles |
| US8518305B2 (en) | 2009-10-28 | 2013-08-27 | Transitions Optical, Inc. | Photochromic materials |
| US9475901B2 (en) * | 2009-12-08 | 2016-10-25 | Transitions Optical, Inc. | Photoalignment materials having improved adhesion |
| JP5278591B2 (ja) * | 2010-02-26 | 2013-09-04 | 株式会社ニコン | パターン形成方法 |
| US8277699B2 (en) | 2010-04-30 | 2012-10-02 | Transistions Optical, Inc. | Photochromic materials that include 6-amino substituted indeno-fused naphthopyrans |
| US8535577B2 (en) | 2010-04-30 | 2013-09-17 | Transitions Optical, Inc. | Photochromic materials that include 6-amino substituted indeno-fused naphthopyrans |
| US9034219B2 (en) | 2010-12-16 | 2015-05-19 | Transitions Optical, Inc. | Photochromic compounds and compositions |
| US8859097B2 (en) | 2010-12-16 | 2014-10-14 | Transitions Optical, Inc. | Photochromic compounds, compositions and articles |
| US8920928B2 (en) | 2010-12-16 | 2014-12-30 | Transitions Optical, Inc. | Photochromic compounds and compositions |
| US9042019B2 (en) | 2011-04-15 | 2015-05-26 | Qspex Technologies, Inc. | Anti-reflective lenses and methods for manufacturing the same |
| US9335443B2 (en) | 2011-04-15 | 2016-05-10 | Qspex Technologies, Inc. | Anti-reflective lenses and methods for manufacturing the same |
| US8641933B2 (en) | 2011-09-23 | 2014-02-04 | Ppg Industries Ohio, Inc | Composite crystal colloidal array with photochromic member |
| US10185057B2 (en) | 2011-11-11 | 2019-01-22 | Ppg Industries Ohio, Inc. | Coated articles having abrasion resistant, glass-like coatings |
| US20140097392A1 (en) * | 2012-10-05 | 2014-04-10 | E I Du Pont De Nemours And Company | Liquid coating compositions of polymer matrix resins with photochromic dyes and films made therefrom |
| US9568643B2 (en) | 2012-12-13 | 2017-02-14 | Ppg Industries Ohio, Inc. | Polyurethane urea-containing compositions and optical articles and methods for preparing them |
| US9081130B1 (en) | 2013-01-09 | 2015-07-14 | Insight Equity A.P.X., Lp | Photochromic polyurethane laminate |
| WO2015032034A1 (en) | 2013-09-04 | 2015-03-12 | Ppg Coatings (Tianjin) Co., Ltd. | Uv-curable coating compositions and methods for using the same |
| WO2015054037A1 (en) * | 2013-10-11 | 2015-04-16 | Transitions Optical, Inc. | Method of preparing a photochromic optical article using an organic solvent pretreatment and photochromic coating |
| JP6496803B2 (ja) * | 2014-07-11 | 2019-04-10 | ドルフ ケタール ケミカルズ (インディア)プライヴェート リミテッド | 接着促進システムおよびそのインク組成物 |
| MX368296B (es) | 2014-09-30 | 2019-09-27 | Transitions Optical Inc | Absorbentes de luz ultravioleta. |
| US10423061B2 (en) | 2015-09-03 | 2019-09-24 | Transitions Optical, Inc. | Multilayer photochromic articles |
| KR102480724B1 (ko) | 2015-10-30 | 2022-12-22 | 트랜지션즈 옵티칼 인코포레이티드 | 구배 광 반응성을 갖는 광학 제품 및 이의 제조 방법 |
| WO2017074429A1 (en) | 2015-10-30 | 2017-05-04 | Transitions Optical Ltd. | A method of making an optical article with an inkjet printing device |
| US10866455B2 (en) | 2017-10-19 | 2020-12-15 | Ppg Industries Ohio, Inc. | Display devices including photochromic-dichroic compounds and dichroic compounds |
| CN112341615B (zh) * | 2020-10-27 | 2021-07-27 | 北京航空航天大学 | 端烃基超支化聚酯以及包含其的光致聚合物材料 |
| CN121241281A (zh) | 2023-06-09 | 2025-12-30 | 全视线光学有限公司 | 光致变色镜片 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637416A (en) * | 1970-02-04 | 1972-01-25 | Mbt Corp | Method of treating synthetic plastic and elastomeric materials and articles produced thereby |
| US3971872A (en) * | 1974-09-30 | 1976-07-27 | American Optical Corporation | Process for the production of an abrasion resistant optical element |
| US4225631A (en) * | 1976-04-19 | 1980-09-30 | Itek Corporation | Abrasion resistant coatings for unsaturated polymeric substrates |
| US4101513A (en) * | 1977-02-02 | 1978-07-18 | Minnesota Mining And Manufacturing Company | Catalyst for condensation of hydrolyzable silanes and storage stable compositions thereof |
| US4348462A (en) * | 1980-07-11 | 1982-09-07 | General Electric Company | Abrasion resistant ultraviolet light curable hard coating compositions |
| JPS57158235A (en) * | 1981-03-26 | 1982-09-30 | Toray Ind Inc | Plastic molding |
| IT1157915B (it) * | 1982-01-13 | 1987-02-18 | Anic Spa | Composizione a base di policarbonato con migliorate caratteristiche meccaniche e mezzi adatti alla sua preparazione |
| US4556605A (en) * | 1982-09-09 | 1985-12-03 | Kabushiki Kaisha Suwa Seikosha | Photochromic coating composition and photochromic synthetic resin ophthalmic lens |
| US4654262A (en) * | 1985-04-10 | 1987-03-31 | Itt Corporation | Polyolefin resin surface preparation |
| US4615947A (en) * | 1985-04-29 | 1986-10-07 | General Electric Company | Acrylic primer for adhering an organopolysiloxane |
| AU564689B2 (en) * | 1985-07-09 | 1987-08-20 | Kureha Kagaku Kogyo K.K. | Photochromic lens |
| JPS6210604A (ja) * | 1985-07-09 | 1987-01-19 | Kureha Chem Ind Co Ltd | 調光レンズ |
| US4673354A (en) * | 1985-10-01 | 1987-06-16 | Minnesota Mining And Manufacturing Company | Stable silanol priming solution for use in dentistry |
| JPS62164537A (ja) * | 1986-01-17 | 1987-07-21 | 東レ株式会社 | 複合体 |
| DE3789547T2 (de) * | 1987-02-13 | 1994-07-14 | Toray Industries | Entspiegelter optischer Gegenstand und Verfahren zu dessen Herstellung. |
| JPH0816211B2 (ja) * | 1989-06-02 | 1996-02-21 | 信越化学工業株式会社 | プライマー組成物 |
| US5104692A (en) * | 1990-04-20 | 1992-04-14 | Pilkington Visioncare Holdings, Inc. | Two-layer antireflective coating applied in solution |
| US5639802A (en) * | 1991-05-20 | 1997-06-17 | Spectra Group Limited, Inc. | Cationic polymerization |
| GB9220986D0 (en) * | 1992-10-06 | 1992-11-18 | Ciba Geigy Ag | Chemical composition |
| US5733483A (en) * | 1995-01-13 | 1998-03-31 | Soane Technologies, Inc. | Method for formation of on-site coated and tinted optical elements |
| JPH08216271A (ja) * | 1995-02-10 | 1996-08-27 | Kureha Chem Ind Co Ltd | 合成樹脂製調光レンズの製造方法 |
| IL118087A (en) * | 1995-05-05 | 1999-05-09 | Innotech Inc | Adhesive photochromic matrix layers for use in optical articles and their preparation |
| US6004486A (en) * | 1995-09-11 | 1999-12-21 | Corning Incorporated | Photochromic spiroxazines with asymmetric monocyclic substituent, compositions and articles containing them |
| IL119781A0 (en) * | 1996-12-08 | 1997-03-18 | Yeda Res & Dev | Photochromic spirooxazine polysiloxanes |
| JP4110306B2 (ja) * | 1998-12-04 | 2008-07-02 | Jsr株式会社 | 防汚性積層体およびその製造方法 |
-
1999
- 1999-07-06 US US09/348,135 patent/US6150430A/en not_active Expired - Lifetime
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2000
- 2000-07-06 AU AU59197/00A patent/AU754726B2/en not_active Ceased
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- 2000-07-06 EP EP00945222A patent/EP1200512B1/en not_active Expired - Lifetime
- 2000-07-06 WO PCT/US2000/018575 patent/WO2001002472A1/en not_active Ceased
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| WO2001002472A1 (en) | 2001-01-11 |
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| BR0012208B1 (pt) | 2012-06-26 |
| BR0012208A (pt) | 2002-07-23 |
| AU754726B2 (en) | 2002-11-21 |
| AU5919700A (en) | 2001-01-22 |
| DE60007753D1 (de) | 2004-02-19 |
| JP2003504438A (ja) | 2003-02-04 |
| US6150430A (en) | 2000-11-21 |
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