ZA200700244B - Methods for producing photosensitive microparticles aqueous compositions thereof and articles prepared therewith - Google Patents
Methods for producing photosensitive microparticles aqueous compositions thereof and articles prepared therewith Download PDFInfo
- Publication number
- ZA200700244B ZA200700244B ZA200700244A ZA200700244A ZA200700244B ZA 200700244 B ZA200700244 B ZA 200700244B ZA 200700244 A ZA200700244 A ZA 200700244A ZA 200700244 A ZA200700244 A ZA 200700244A ZA 200700244 B ZA200700244 B ZA 200700244B
- Authority
- ZA
- South Africa
- Prior art keywords
- photochromic
- photosensitive
- polymeric
- microparticles
- article
- Prior art date
Links
- 239000011859 microparticle Substances 0.000 title claims description 86
- 239000000203 mixture Substances 0.000 title claims description 86
- 238000000034 method Methods 0.000 title claims description 32
- 239000000463 material Substances 0.000 claims description 269
- 239000000178 monomer Substances 0.000 claims description 149
- 230000002209 hydrophobic effect Effects 0.000 claims description 80
- -1 masonry Substances 0.000 claims description 59
- 230000003287 optical effect Effects 0.000 claims description 31
- 229920000642 polymer Polymers 0.000 claims description 24
- 125000000524 functional group Chemical group 0.000 claims description 21
- 230000002441 reversible effect Effects 0.000 claims description 21
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 20
- 230000009477 glass transition Effects 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 15
- 239000012948 isocyanate Substances 0.000 claims description 12
- 150000002513 isocyanates Chemical class 0.000 claims description 12
- 150000004880 oxines Chemical class 0.000 claims description 12
- 239000011368 organic material Substances 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 8
- 239000006185 dispersion Substances 0.000 claims description 8
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 238000004132 cross linking Methods 0.000 claims description 6
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- 239000004417 polycarbonate Substances 0.000 claims description 5
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
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- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 3
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- 229910052684 Cerium Inorganic materials 0.000 claims description 2
- 229910052693 Europium Inorganic materials 0.000 claims description 2
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- 239000010949 copper Substances 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 claims description 2
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- 239000004332 silver Substances 0.000 claims description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 2
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- 238000000576 coating method Methods 0.000 claims 10
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- 230000001070 adhesive effect Effects 0.000 claims 7
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- 239000004416 thermosoftening plastic Substances 0.000 claims 7
- 229920001187 thermosetting polymer Polymers 0.000 claims 5
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 230000000379 polymerizing effect Effects 0.000 claims 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- 238000005299 abrasion Methods 0.000 claims 3
- 239000000919 ceramic Substances 0.000 claims 3
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- 239000004814 polyurethane Substances 0.000 claims 3
- SKESERDUDQOXKM-UHFFFAOYSA-N 2-methylprop-2-enoic acid;phenol Chemical class CC(=C)C(O)=O.CC(=C)C(O)=O.OC1=CC=CC=C1 SKESERDUDQOXKM-UHFFFAOYSA-N 0.000 claims 2
- OOXMQACSWCZQLX-UHFFFAOYSA-N 3,9-bis(ethenyl)-2,4,8,10-tetraoxaspiro[5.5]undecane Chemical compound C1OC(C=C)OCC21COC(C=C)OC2 OOXMQACSWCZQLX-UHFFFAOYSA-N 0.000 claims 2
- 229920008347 Cellulose acetate propionate Polymers 0.000 claims 2
- 229920002284 Cellulose triacetate Polymers 0.000 claims 2
- 239000004793 Polystyrene Substances 0.000 claims 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 claims 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 claims 2
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 claims 2
- QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical class C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 claims 2
- 229920002301 cellulose acetate Polymers 0.000 claims 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims 2
- 125000005702 oxyalkylene group Chemical group 0.000 claims 2
- 239000000123 paper Substances 0.000 claims 2
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical class CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 claims 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims 2
- 229920001223 polyethylene glycol Polymers 0.000 claims 2
- 229920000139 polyethylene terephthalate Polymers 0.000 claims 2
- 239000005020 polyethylene terephthalate Substances 0.000 claims 2
- 229920002223 polystyrene Polymers 0.000 claims 2
- 229920002578 polythiourethane polymer Polymers 0.000 claims 2
- 229920002689 polyvinyl acetate Polymers 0.000 claims 2
- 239000011118 polyvinyl acetate Substances 0.000 claims 2
- 239000004753 textile Substances 0.000 claims 2
- 239000002023 wood Substances 0.000 claims 2
- HIACAHMKXQESOV-UHFFFAOYSA-N 1,2-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=CC=C1C(C)=C HIACAHMKXQESOV-UHFFFAOYSA-N 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 229920002732 Polyanhydride Polymers 0.000 claims 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims 1
- SGPGESCZOCHFCL-UHFFFAOYSA-N Tilisolol hydrochloride Chemical compound [Cl-].C1=CC=C2C(=O)N(C)C=C(OCC(O)C[NH2+]C(C)(C)C)C2=C1 SGPGESCZOCHFCL-UHFFFAOYSA-N 0.000 claims 1
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 claims 1
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- 239000006117 anti-reflective coating Substances 0.000 claims 1
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- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
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- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims 1
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- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 claims 1
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- VFMUXPQZKOKPOF-UHFFFAOYSA-N 2,3,7,8,12,13,17,18-octaethyl-21,23-dihydroporphyrin platinum Chemical compound [Pt].CCc1c(CC)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(CC)c5CC)c(CC)c4CC)c(CC)c3CC VFMUXPQZKOKPOF-UHFFFAOYSA-N 0.000 description 3
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Classifications
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
-
- 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
- C08G18/757—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 at least two isocyanate or isothiocyanate groups linked to the cycloaliphatic ring by means of an aliphatic group
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- 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
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- 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
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- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/23—Photochromic filters
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
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- Life Sciences & Earth Sciences (AREA)
- Structural Engineering (AREA)
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- Optics & Photonics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Eyeglasses (AREA)
- Polymerisation Methods In General (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Optical Filters (AREA)
- Polyurethanes Or Polyureas (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (1)
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| US10/892,919 US8153344B2 (en) | 2004-07-16 | 2004-07-16 | Methods for producing photosensitive microparticles, aqueous compositions thereof and articles prepared therewith |
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| ZA200700244B true ZA200700244B (en) | 2008-05-28 |
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| ZA200700244A ZA200700244B (en) | 2004-07-16 | 2007-01-09 | Methods for producing photosensitive microparticles aqueous compositions thereof and articles prepared therewith |
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| US (1) | US8153344B2 (zh) |
| EP (1) | EP1778815B1 (zh) |
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| ZA (1) | ZA200700244B (zh) |
Families Citing this family (119)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8389113B2 (en) * | 2002-09-17 | 2013-03-05 | Ppg Industries Ohio, Inc. | Substrates and articles of manufacture coated with a waterborne 2K coating composition |
| US20070020463A1 (en) * | 2004-12-23 | 2007-01-25 | Trainham James A | Flexible polymer coating and coated flexible substrates |
| US7057134B2 (en) * | 2003-03-18 | 2006-06-06 | Loma Linda University Medical Center | Laser manipulation system for controllably moving a laser head for irradiation and removal of material from a surface of a structure |
| US7605194B2 (en) | 2003-06-24 | 2009-10-20 | Ppg Industries Ohio, Inc. | Aqueous dispersions of polymer-enclosed particles, related coating compositions and coated substrates |
| US20080112909A1 (en) * | 2003-06-24 | 2008-05-15 | Ppg Industries Ohio, Inc. | Compositions for providing color to animate objects and related methods |
| US20100184911A1 (en) * | 2009-01-22 | 2010-07-22 | Ppg Industries Ohio, Inc. | Aqueous dispersions of polymer-enclosed particles, related coating compositions and coated substrates |
| US8563213B2 (en) * | 2004-07-16 | 2013-10-22 | Transitions Optical, Inc. | Methods for producing photosensitive microparticles |
| US8563212B2 (en) * | 2004-07-16 | 2013-10-22 | Transitions Optical, Inc. | Methods for producing photosensitive microparticles, non-aqueous dispersions thereof and articles prepared therewith |
| JP5272332B2 (ja) * | 2006-06-28 | 2013-08-28 | 東レ株式会社 | 蛍光体ペーストおよびディスプレイの製造方法 |
| US8349066B2 (en) | 2006-09-21 | 2013-01-08 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US20080095933A1 (en) * | 2006-10-18 | 2008-04-24 | Colton James P | Process for preparing coated optical elements |
| US20080096023A1 (en) * | 2006-10-18 | 2008-04-24 | Ppg Industries Ohio, Inc. | Process for preparing coated optical elements |
| FR2909094A1 (fr) * | 2006-11-28 | 2008-05-30 | Arkema France | Memoire optique 3d comprenant des particules multicouches comprenant un monomere photoactif porteur d'un groupement photoisomerisable. |
| US7667285B2 (en) * | 2006-12-14 | 2010-02-23 | Motorola, Inc. | Printed electronic substrate havine photochromic barrier layer |
| US20080187749A1 (en) * | 2007-01-11 | 2008-08-07 | Ppg Industries Ohio, Inc. | Optical element having light influencing property |
| US7852366B2 (en) * | 2007-06-13 | 2010-12-14 | Xerox Corporation | System and method for printing reimageable transient documents |
| US20080311493A1 (en) * | 2007-06-13 | 2008-12-18 | Xerox Corporation | Inkless reimageable printing paper and method |
| US8097093B2 (en) | 2007-09-28 | 2012-01-17 | Ppg Industries Ohio, Inc | Methods for treating a ferrous metal substrate |
| US9428410B2 (en) | 2007-09-28 | 2016-08-30 | Ppg Industries Ohio, Inc. | Methods for treating a ferrous metal substrate |
| US20090246393A1 (en) * | 2008-03-27 | 2009-10-01 | Ppg Industries Ohio, Inc. | Polycarbodiimides |
| US8507050B2 (en) * | 2008-11-12 | 2013-08-13 | Ppg Industries Ohio, Inc. | Methods for depositing ultra thin coatings exhibiting low haze and methods for the preparation of such coatings |
| KR101002659B1 (ko) * | 2008-12-23 | 2010-12-20 | 삼성모바일디스플레이주식회사 | 유기 발광 표시 장치 |
| FR2940975B1 (fr) | 2009-01-13 | 2011-02-25 | Centre Nat Rech Scient | Materiau composite photochrome |
| US8575927B2 (en) | 2009-01-16 | 2013-11-05 | Toyota Jidosha Kabushiki Kaisha | Ultrasensitive magnetic sensor with magneto-optically active material with high verdet constant |
| EP2462177B2 (de) * | 2009-08-06 | 2018-08-08 | Basf Se | Strahlungshärtbare wasserdispergierbare polyurethane und polyurethandispersionen |
| US8143348B2 (en) | 2009-09-01 | 2012-03-27 | Ppg Industries Ohio, Inc. | Waterborne coating compositions, related methods and coated substrates |
| US8900667B2 (en) | 2009-12-18 | 2014-12-02 | Ppg Industries Ohio, Inc. | One-component, ambient curable waterborne coating compositions, related methods and coated substrates |
| US8461253B2 (en) | 2010-01-15 | 2013-06-11 | Ppg Industries Ohio, Inc. | One-component, ambient curable waterborne coating compositions, related methods and coated substrates |
| KR101188678B1 (ko) * | 2010-01-26 | 2012-10-08 | 주식회사 에이앤피 테크 | 광학부재 및 그 제조방법 |
| US8323871B2 (en) * | 2010-02-24 | 2012-12-04 | International Business Machines Corporation | Antireflective hardmask composition and a method of preparing a patterned material using same |
| WO2011109386A1 (en) | 2010-03-02 | 2011-09-09 | Ppg Industries Ohio, Inc. | One-component, ambient curable waterborne coating compositions, related methods and coated substrates |
| JP5931921B2 (ja) | 2011-01-12 | 2016-06-08 | ケンブリッジ エンタープライズ リミテッド | 複合光学材料の製造 |
| US10451897B2 (en) | 2011-03-18 | 2019-10-22 | Johnson & Johnson Vision Care, Inc. | Components with multiple energization elements for biomedical devices |
| WO2012166253A2 (en) | 2011-05-31 | 2012-12-06 | Sdc Technologies, Inc. | Anti-fog polyurethane coating compositions |
| US10017861B2 (en) | 2011-08-03 | 2018-07-10 | Ppg Industries Ohio, Inc. | Zirconium pretreatment compositions containing a rare earth metal, associated methods for treating metal substrates, and related coated metal substrates |
| US9022562B2 (en) | 2011-08-05 | 2015-05-05 | Nitto Denko Corporation | Optical element for correcting color blindness |
| US8852357B2 (en) | 2011-09-30 | 2014-10-07 | Ppg Industries Ohio, Inc | Rheology modified pretreatment compositions and associated methods of use |
| US8845873B2 (en) | 2011-09-30 | 2014-09-30 | Ppg Industries Ohio, Inc. | Near neutral buoyancy texture additive for electrodepositable coating compositions and associated methods for forming textured coated substrates |
| FR2983487B1 (fr) | 2011-12-06 | 2015-02-20 | Centre Nat Rech Scient | Compositions de materiaux photocommutables. |
| US8857983B2 (en) | 2012-01-26 | 2014-10-14 | Johnson & Johnson Vision Care, Inc. | Ophthalmic lens assembly having an integrated antenna structure |
| IL224797A (en) * | 2012-02-22 | 2017-03-30 | Johnson & Johnson Vision Care | An eyepiece lens with annular layers divided by a functional implant |
| US20130302620A1 (en) | 2012-05-09 | 2013-11-14 | Ppg Industries Ohio, Inc. | Basecoat with improved adhesion to bioplastic |
| US8758862B2 (en) | 2012-06-26 | 2014-06-24 | Prc Desoto International, Inc. | Coating compositions with an isocyanate-functional prepolymer derived from a tricyclodecane polyol, methods for their use, and related coated substrates |
| EP2871216A4 (en) * | 2012-07-06 | 2016-03-02 | Mitsui Chemicals Inc | POLYMER PARTICLES AND THEIR USE |
| AU2013309270B2 (en) | 2012-08-29 | 2016-03-17 | Ppg Industries Ohio, Inc. | Zirconium pretreatment compositions containing molybdenum, associated methods for treating metal substrates, and related coated metal substrates |
| CN104685099A (zh) | 2012-08-29 | 2015-06-03 | Ppg工业俄亥俄公司 | 含锂的锆预处理组合物,处理金属基材的相关方法,和相关的经涂覆的金属基材 |
| US9109131B2 (en) * | 2013-01-16 | 2015-08-18 | Xerox Corporation | Photochromic phase change ink compositions |
| US8931930B2 (en) | 2013-01-29 | 2015-01-13 | Nitto Denko Corporation | Optical element for correcting color blindness |
| US9303167B2 (en) | 2013-03-15 | 2016-04-05 | Ppg Industries Ohio, Inc. | Method for preparing and treating a steel substrate |
| US9068089B2 (en) | 2013-03-15 | 2015-06-30 | Ppg Industries Ohio, Inc. | Phenolic admix for electrodepositable coating composition containing a cyclic guanidine |
| PL3041908T3 (pl) | 2013-09-04 | 2019-04-30 | Ppg Coatings Tianjin Co Ltd | Kompozycje powłokowe utwardzalne UV i sposoby ich zastosowania |
| US9311545B2 (en) | 2013-09-18 | 2016-04-12 | Blackberry Limited | Multicolor biometric scanning user interface |
| US9418273B2 (en) | 2013-09-18 | 2016-08-16 | Blackberry Limited | Structure for multicolor biometric scanning user interface |
| US20150132592A1 (en) | 2013-11-08 | 2015-05-14 | Ppg Industries Ohio, Inc. | Curable film-forming compositions comprising catalyst associated with a carrier and methods for coating a substrate |
| US9562000B2 (en) | 2014-02-14 | 2017-02-07 | Prc-Desoto International, Inc. | Amino alcohol treatment for sol-gel conversion coatings, substrates including the same, and methods of making the substrates |
| JP6256132B2 (ja) * | 2014-03-14 | 2018-01-10 | 株式会社リコー | 撮像システム |
| WO2015140968A1 (ja) * | 2014-03-19 | 2015-09-24 | 株式会社メニコン | 含水性コンタクトレンズ用インク組成物 |
| KR101958195B1 (ko) * | 2014-04-15 | 2019-03-14 | 아그파 엔브이 | 수성 수지계 잉크젯 잉크 |
| EP4369080A3 (en) | 2014-06-25 | 2024-07-17 | Hoya Optical Labs Of America, Inc | Dye microenvironment |
| US10381687B2 (en) | 2014-08-21 | 2019-08-13 | Johnson & Johnson Vision Care, Inc. | Methods of forming biocompatible rechargable energization elements for biomedical devices |
| US10627651B2 (en) | 2014-08-21 | 2020-04-21 | Johnson & Johnson Vision Care, Inc. | Methods and apparatus to form biocompatible energization primary elements for biomedical devices with electroless sealing layers |
| US9793536B2 (en) | 2014-08-21 | 2017-10-17 | Johnson & Johnson Vision Care, Inc. | Pellet form cathode for use in a biocompatible battery |
| US9941547B2 (en) | 2014-08-21 | 2018-04-10 | Johnson & Johnson Vision Care, Inc. | Biomedical energization elements with polymer electrolytes and cavity structures |
| US9715130B2 (en) | 2014-08-21 | 2017-07-25 | Johnson & Johnson Vision Care, Inc. | Methods and apparatus to form separators for biocompatible energization elements for biomedical devices |
| US9383593B2 (en) | 2014-08-21 | 2016-07-05 | Johnson & Johnson Vision Care, Inc. | Methods to form biocompatible energization elements for biomedical devices comprising laminates and placed separators |
| US10361405B2 (en) | 2014-08-21 | 2019-07-23 | Johnson & Johnson Vision Care, Inc. | Biomedical energization elements with polymer electrolytes |
| US10361404B2 (en) | 2014-08-21 | 2019-07-23 | Johnson & Johnson Vision Care, Inc. | Anodes for use in biocompatible energization elements |
| US9599842B2 (en) | 2014-08-21 | 2017-03-21 | Johnson & Johnson Vision Care, Inc. | Device and methods for sealing and encapsulation for biocompatible energization elements |
| KR101959408B1 (ko) * | 2014-11-12 | 2019-03-18 | 삼성에스디아이 주식회사 | 표시장치 절연막 및 이를 포함하는 유기 발광 장치 |
| JP6460391B2 (ja) * | 2015-02-17 | 2019-01-30 | 国立大学法人 鹿児島大学 | フォトクロミック微粒子の製造方法、及びフォトクロミック微粒子 |
| US10017690B2 (en) * | 2015-05-28 | 2018-07-10 | Xerox Corporation | Photochromatic composition for 3D printing |
| US10113070B2 (en) | 2015-11-04 | 2018-10-30 | Ppg Industries Ohio, Inc. | Pretreatment compositions and methods of treating a substrate |
| US20170204289A1 (en) | 2016-01-15 | 2017-07-20 | Ppg Industries Ohio, Inc. | Hydroxy functional alkyl polyurea |
| EP3402853A1 (en) | 2016-01-15 | 2018-11-21 | PPG Industries Ohio, Inc. | A coating composition comprising a powder dispersed in a liquid carrier |
| US10345620B2 (en) | 2016-02-18 | 2019-07-09 | Johnson & Johnson Vision Care, Inc. | Methods and apparatus to form biocompatible energization elements incorporating fuel cells for biomedical devices |
| AT518601A1 (de) * | 2016-05-09 | 2017-11-15 | Franz Schwarz Hubert | Anstrichmittel |
| CA3026419A1 (en) * | 2016-05-11 | 2017-11-16 | Neenah, Inc. | Security document having enhanced foil durability |
| US10421874B2 (en) | 2016-06-30 | 2019-09-24 | Ppg Industries Ohio, Inc. | Electrodepositable coating composition having improved crater control |
| CN106220780B (zh) * | 2016-08-09 | 2019-07-12 | 上海交通大学 | 一种变色龙仿生的迷彩伪装变色膜的制备方法 |
| MX2019001777A (es) | 2016-08-19 | 2019-12-11 | Strauss Levi & Co | Acabado laser de prenda de vestir. |
| RU2729485C1 (ru) | 2016-08-24 | 2020-08-07 | Ппг Индастриз Огайо, Инк. | Железосодержащая композиция очистителя |
| US10184068B2 (en) | 2016-09-28 | 2019-01-22 | Ppg Industries Ohio, Inc. | Coating compositions comprising silicone |
| US10703920B2 (en) | 2016-09-28 | 2020-07-07 | Ppg Industries Ohio, Inc. | Corrosion-resistant epoxidized vegetable oil can interior coating |
| JP6542982B2 (ja) | 2016-10-11 | 2019-07-10 | 三井化学株式会社 | 光学材料用重合性組成物およびその用途 |
| JP6810792B2 (ja) * | 2017-03-31 | 2021-01-06 | 三井化学株式会社 | 積層体の製造方法、積層体およびハードコート液 |
| US10808144B2 (en) | 2017-05-22 | 2020-10-20 | Ppg Industries Ohio, Inc. | Polyolefin silicon coating composition |
| JP2019006891A (ja) * | 2017-06-23 | 2019-01-17 | トーヨーポリマー株式会社 | 防曇コーティング組成物及びそれを用いた防曇性透明シート |
| US10392515B2 (en) | 2017-08-25 | 2019-08-27 | Ppg Industries Ohio, Inc. | Metal cans coated with shellac-containing coatings |
| US10370545B2 (en) | 2017-09-19 | 2019-08-06 | Ppg Industries Ohio, Inc. | Low VOC anionic electrodepositable coating composition |
| US10738213B2 (en) | 2017-10-17 | 2020-08-11 | Ppg Industries Ohio, Inc. | Modified silicone coating composition |
| CN111527493A (zh) | 2017-10-31 | 2020-08-11 | 利惠商业有限公司 | 在创建服饰设计时使用神经网络 |
| EP3703898A4 (en) | 2017-10-31 | 2021-05-19 | Levi Strauss & Co. | LASER PROCESSING TOOL |
| US11053191B2 (en) | 2018-01-09 | 2021-07-06 | Ppg Industries Ohio, Inc. | Hydroxy functional alkyl carbamate crosslinkers |
| WO2019145782A2 (en) | 2018-01-23 | 2019-08-01 | Clear and Dark Ltd. | Systems, methods, and apparatus for forming optical articles, and optical articles formed by the same |
| CN112262363A (zh) | 2018-02-27 | 2021-01-22 | 利惠商业有限公司 | 激光整理设计工具 |
| CN112272596B (zh) | 2018-02-27 | 2023-06-23 | 利惠商业有限公司 | 激光整理服装的按需制造 |
| US11299576B2 (en) | 2018-05-11 | 2022-04-12 | Carbon, Inc. | Sustainable chemistry systems for recyclable dental models and other additively manufactured products |
| US10947408B2 (en) | 2018-06-27 | 2021-03-16 | Prc-Desoto International, Inc. | Electrodepositable coating composition |
| US11022722B2 (en) * | 2018-07-03 | 2021-06-01 | Bausch & Lomb Incorporated | Water extractable ophthalmic devices |
| US10883223B2 (en) | 2018-08-07 | 2021-01-05 | Levi Strauss & Co. | Laser finishing design tool |
| ES2946141T3 (es) * | 2018-08-10 | 2023-07-13 | Bausch & Lomb | Dispositivos oftálmicos con alto contenido en agua |
| JP7357056B2 (ja) * | 2018-08-10 | 2023-10-05 | ボシュ・アンド・ロム・インコーポレイテッド | 眼科用デバイス |
| US20200095448A1 (en) | 2018-09-21 | 2020-03-26 | Ppg Industries Ohio, Inc. | Coating Composition Providing Increased Adhesion and/or UV Durability to a Substrate |
| WO2020113236A1 (en) | 2018-11-30 | 2020-06-04 | Levi Strauss & Co. | Shadow neutral 3-d garment rendering |
| CN109875171B (zh) * | 2019-01-30 | 2024-05-03 | 国家电网公司 | 电场感应报警安全帽 |
| CN113348223B (zh) | 2019-01-30 | 2024-08-09 | 三井化学株式会社 | 光学材料用聚合性组合物的制造方法 |
| TWI709789B (zh) * | 2019-03-28 | 2020-11-11 | 星歐光學股份有限公司 | 隱形眼鏡及隱形眼鏡產品 |
| US20200325289A1 (en) | 2019-04-15 | 2020-10-15 | Ppg Industries Ohio, Inc. | Curable film-forming compositions containing rheology modifiers comprising non-aqueous dispersions |
| US11313048B2 (en) | 2019-06-27 | 2022-04-26 | Prc-Desoto International, Inc. | Addition polymer for electrodepositable coating compositions |
| US11485874B2 (en) | 2019-06-27 | 2022-11-01 | Prc-Desoto International, Inc. | Addition polymer for electrodepositable coating compositions |
| US11274167B2 (en) | 2019-06-27 | 2022-03-15 | Prc-Desoto International, Inc. | Carbamate functional monomers and polymers and use thereof |
| CN114423896A (zh) | 2019-07-23 | 2022-04-29 | 利惠商业有限公司 | 对激光精加工服装的三维渲染预览 |
| US20220325133A1 (en) * | 2019-08-30 | 2022-10-13 | Transitions Optical, Ltd. | Photochromic Composition with Polyol and Poly(anhydride) |
| WO2021108760A1 (en) * | 2019-11-26 | 2021-06-03 | Virginia Commonwealth University | Slug-flow manufacturing of uniform and controllable microparticles for battery cathodes |
| CN115768746A (zh) | 2020-05-28 | 2023-03-07 | 株式会社德山 | 光学材料用化合物、固化性组合物、固化物和光学物品 |
| JP2023529241A (ja) | 2020-06-01 | 2023-07-07 | アイケアーズ メディカス インコーポレイテッド | 両面非球面回折多焦点レンズ、その製造、および使用 |
| KR102417069B1 (ko) * | 2022-03-24 | 2022-07-05 | 함병우 | 회전형 교반기를 이용한 실리콘 잉크 제조방법 |
| WO2024054786A1 (en) | 2022-09-06 | 2024-03-14 | Ppg Industries Ohio, Inc. | Precision coatings and methods of applying them |
| WO2024091839A1 (en) | 2022-10-26 | 2024-05-02 | Ppg Industries Ohio, Inc. | Coating composition for use in high efficiency applicators |
Family Cites Families (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US108935A (en) | 1870-11-01 | Improvement in steam-generators | ||
| US108936A (en) | 1870-11-01 | Improvement in steam-generators | ||
| US4046729A (en) * | 1975-06-02 | 1977-09-06 | Ppg Industries, Inc. | Water-reduced urethane coating compositions |
| FR2480764B1 (fr) * | 1980-04-18 | 1985-10-04 | Rhone Poulenc Spec Chim | Latex de polymeres magnetiques et procede de preparation |
| US4533254A (en) * | 1981-04-17 | 1985-08-06 | Biotechnology Development Corporation | Apparatus for forming emulsions |
| US4556605A (en) * | 1982-09-09 | 1985-12-03 | Kabushiki Kaisha Suwa Seikosha | Photochromic coating composition and photochromic synthetic resin ophthalmic lens |
| US4685783A (en) * | 1983-09-07 | 1987-08-11 | The Plessey Company P.L.C. | Polychromic tetracyclo-spiro-adamatylidene derivatives, and polychromic lens incorporating said compounds |
| US4546045A (en) * | 1984-12-27 | 1985-10-08 | Ppg Industries, Inc. | Method for reducing temperature rise of heat sensitive substrates |
| US4681811A (en) * | 1985-08-19 | 1987-07-21 | Ppg Industries, Inc. | Color plus clear coatings employing polyepoxides and polyacid curing agents in the clear coat |
| US4732790A (en) * | 1986-08-21 | 1988-03-22 | Ppg Industries, Inc. | Color plus clear application of thermosetting high solids coating composition of hydroxy-functional epoxies and anhydrides |
| AU616650B2 (en) | 1987-02-02 | 1991-11-07 | Toray Industries, Inc. | Spirooxazine photochromic compounds and resins |
| CA1340939C (en) * | 1987-02-02 | 2000-03-28 | Ryojiro Akashi | Photochromic compound |
| DE3706561A1 (de) * | 1987-02-28 | 1988-09-08 | Basf Ag | Lichtempfindliches aufzeichnungsmaterial mit erhoehter flexibilitaet |
| JPH07121977B2 (ja) | 1987-07-24 | 1995-12-25 | 東レ株式会社 | フォトクロミック性ポリマ−微粒子 |
| US4798746A (en) * | 1987-08-24 | 1989-01-17 | Ppg Industries, Inc. | Basecoat/clearcoat method of coating utilizing an anhydride additive in the thermoplastic polymer-containing basecoat for improved repairability |
| EP0310139A3 (en) * | 1987-10-02 | 1990-10-31 | Fuji Photo Film Co., Ltd. | Light-sensitive microcapsule and light-sensitive material employing the same |
| US4931220A (en) * | 1987-11-24 | 1990-06-05 | Ppg Industries, Inc. | Organic photochromic pigment particulates |
| US5017225A (en) * | 1987-12-02 | 1991-05-21 | Japan Capsular Products Inc. | Microencapsulated photochromic material, process for its preparation and a water-base ink composition prepared therefrom |
| JPH0621257B2 (ja) * | 1988-07-14 | 1994-03-23 | 株式会社タカ・コーポレーション | 耐光性フォトクロミックインキの製造方法 |
| FR2645160B1 (zh) * | 1989-03-31 | 1992-10-02 | Rhone Poulenc Chimie | |
| US5071904A (en) * | 1989-05-30 | 1991-12-10 | Ppg Industries, Inc. | Waterborne coating compositions for automotive applications |
| DE3924811A1 (de) * | 1989-07-27 | 1991-01-31 | Hoechst Ag | Pfropfpolymerisat mit ungesaettigten seitenketten, dieses enthaltendes lichtempfindliches gemisch sowie daraus hergestelltes aufzeichnungsmaterial |
| US5143997A (en) * | 1989-10-11 | 1992-09-01 | Daicel Chemical Industries, Ltd. | Polycarbonate-polyol composition and polycarbonate(meth) acrylate compositions and urethane(meth) acrylate compositions prepared therefrom |
| JPH0816215B2 (ja) * | 1990-06-18 | 1996-02-21 | 株式会社松井色素化学工業所 | フォトクロミック材料 |
| JPH04117483A (ja) | 1990-09-06 | 1992-04-17 | Nikon Corp | フォトクロミック・プラスチック成形物 |
| US5221288A (en) * | 1990-10-09 | 1993-06-22 | Matsui Shikiso Chemical Co., Ltd. | Thermochromic dyeing method and cellulose product dyed thereby |
| US5252450A (en) * | 1991-02-06 | 1993-10-12 | Battelle Memorial Institute | Capped photochromic silver halides for incorporation into a plastic matrix |
| US5639802A (en) * | 1991-05-20 | 1997-06-17 | Spectra Group Limited, Inc. | Cationic polymerization |
| US5246748A (en) * | 1991-12-23 | 1993-09-21 | Hoechst Celanese Corp. | Thin film optical medium of a multiple amphiphilic bilayer composite |
| CA2092225A1 (en) * | 1992-03-24 | 1993-09-25 | Yasuhiko Nakae | Polyfunctional polycarbonate polyol |
| JPH06256758A (ja) | 1993-03-10 | 1994-09-13 | Mitsubishi Petrochem Co Ltd | フォトクロミック材料 |
| JPH0726027A (ja) | 1993-07-12 | 1995-01-27 | Nikon Corp | フォトクロミック・プラスチック成形物 |
| JPH0762337A (ja) | 1993-08-23 | 1995-03-07 | Toray Ind Inc | 液晶性高分子フォトクロミック材料 |
| US5458814A (en) * | 1993-12-09 | 1995-10-17 | Transitions Optical, Inc. | Substituted naphthopyrans |
| JPH07258585A (ja) * | 1994-03-18 | 1995-10-09 | Nippon Paint Co Ltd | 水性塗料組成物及び色彩可変塗膜 |
| JPH07258581A (ja) * | 1994-03-18 | 1995-10-09 | Nippon Paint Co Ltd | フォトクロミック性光輝顔料及びそれを含むコーティング組成物 |
| US5468802A (en) * | 1994-07-18 | 1995-11-21 | Ppg Industries, Inc. | Low volatile organic content automotive refinish coating composition |
| US5631382A (en) * | 1994-08-08 | 1997-05-20 | Tokuyama Corporation | Fulgimide compound |
| US5645767A (en) * | 1994-11-03 | 1997-07-08 | Transitions Optical, Inc. | Photochromic indeno-fused naphthopyrans |
| US5658501A (en) * | 1995-06-14 | 1997-08-19 | Transitions Optical, Inc. | Substituted naphthopyrans |
| RU2095836C1 (ru) | 1995-07-20 | 1997-11-10 | Войсковая часть 33825 | Способ получения микрокапсул с органическим фотохромным соединением в полимерной матрице |
| US5723072A (en) * | 1996-06-17 | 1998-03-03 | Ppg Industries, Inc. | Photochromic heterocyclic fused indenonaphthopyrans |
| US5698141A (en) * | 1996-06-17 | 1997-12-16 | Ppg Industries, Inc. | Photochromic heterocyclic fused indenonaphthopyrans |
| FR2751971B1 (fr) * | 1996-07-31 | 1998-11-20 | Essilor Int | Nouvelles spirooxazines homoazaadamantane et leur utilisation dans le domaine de l'optique ophtalmique |
| CA2281495C (en) * | 1997-02-21 | 2003-10-07 | Ppg Industries Ohio, Inc. | Photochromic polyurethane coating and articles having such a coating |
| US6025026A (en) * | 1997-06-30 | 2000-02-15 | Transitions Optical, Inc. | Process for producing an adherent polymeric layer on polymeric substrates and articles produced thereby |
| US6268055B1 (en) * | 1997-12-08 | 2001-07-31 | Ppg Industries Ohio, Inc. | Photochromic epoxy resin coating composition and articles having such a coating |
| US5879592A (en) * | 1997-12-10 | 1999-03-09 | Ppg Industries, Inc. | Water soluble photochromic compounds, compositions and optical elements comprising the compounds |
| US6630597B1 (en) * | 1997-12-15 | 2003-10-07 | Transitions Optical, Inc. | Photochromic 6-aryl substituted 3H-naphtho(2,1-b)pyrans |
| ES2241262T3 (es) * | 1998-02-18 | 2005-10-16 | Ppg Industries Ohio, Inc. | Composicion de recubrimiento compuesta de multicomponentes y sustrato recubierto. |
| US5919846A (en) * | 1998-02-19 | 1999-07-06 | Milliken Research Corporation | Colorant having isocyanate substituent |
| US5952131A (en) * | 1998-04-27 | 1999-09-14 | Xerox Corporation | Core and shell matrix compositions and processes |
| DE19820302A1 (de) * | 1998-05-04 | 2000-02-24 | Basf Ag | Kern/Schale-Partikel, ihre Herstellung und Verwendung |
| DE69903042T2 (de) * | 1998-07-10 | 2003-08-07 | Transitions Optical, Inc. | Photochrome sechsgliedrige heterocyclisch kondensierte naphthopyrane |
| US6022497A (en) * | 1998-07-10 | 2000-02-08 | Ppg Industries Ohio, Inc. | Photochromic six-membered heterocyclic-fused naphthopyrans |
| US6555028B2 (en) * | 1998-09-11 | 2003-04-29 | Transitions Optical, Inc. | Polymeric matrix compatibilized naphthopyrans |
| AU761180B2 (en) * | 1998-09-11 | 2003-05-29 | Transitions Optical, Inc | Polymerizable polyalkoxylated naphthopyrans |
| US6436525B1 (en) * | 1998-12-11 | 2002-08-20 | Ppg Industries Ohio, Inc. | Polyanhydride photochromic coating composition and photochromic articles |
| US6180181B1 (en) * | 1998-12-14 | 2001-01-30 | Ppg Industries Ohio, Inc. | Methods for forming composite coatings on substrates |
| US6060001A (en) * | 1998-12-14 | 2000-05-09 | Ppg Industries Ohio, Inc. | Alkoxyacrylamide photochromic coatings compositions and photochromic articles |
| US6506488B1 (en) * | 1998-12-18 | 2003-01-14 | Ppg Industries Ohio, Inc. | Aminoplast resin photochromic coating composition and photochromic articles |
| US6432544B1 (en) * | 1998-12-18 | 2002-08-13 | Ppg Industries Ohio, Inc. | Aminoplast resin photochromic coating composition and photochromic articles |
| FR2790264A1 (fr) | 1999-02-26 | 2000-09-01 | Essilor Int | Procede de preparation d'un latex a proprietes photochromiques et ses applications, en particulier dans le domaine ophtalmique |
| AU769459C (en) | 1999-03-16 | 2004-07-22 | Zms, Llc | Precision integral articles |
| US6338808B1 (en) * | 1999-03-31 | 2002-01-15 | Fuji Photo Film Co., Ltd. | Liquid crystal composition comprising liquid crystal molecules and alignment promoter |
| US6325957B1 (en) * | 1999-06-04 | 2001-12-04 | The Governing Council Of The University Of Toronto | Method of producing three dimensional assembly of particles in ordered arrays |
| BR0012206B1 (pt) * | 1999-07-02 | 2010-08-24 | artigo fotocrâmico revestido e artigo fotocrâmico. | |
| US6150430A (en) * | 1999-07-06 | 2000-11-21 | Transitions Optical, Inc. | Process for adhering a photochromic coating to a polymeric substrate |
| EP1203118A1 (en) * | 1999-07-19 | 2002-05-08 | Nano-Tex LLC | Nanoparticle-based permanent treatments for textiles |
| US6524164B1 (en) | 1999-09-14 | 2003-02-25 | Applied Materials, Inc. | Polishing pad with transparent window having reduced window leakage for a chemical mechanical polishing apparatus |
| US6348604B1 (en) * | 1999-09-17 | 2002-02-19 | Ppg Industries Ohio, Inc. | Photochromic naphthopyrans |
| US6296785B1 (en) * | 1999-09-17 | 2001-10-02 | Ppg Industries Ohio, Inc. | Indeno-fused photochromic naphthopyrans |
| US6329060B1 (en) * | 1999-11-10 | 2001-12-11 | Ppg Industries Ohio, Inc. | Solvent-free film-forming compositions for clearcoats, coated substrates and method related thereto |
| US6353102B1 (en) * | 1999-12-17 | 2002-03-05 | Ppg Industries Ohio, Inc. | Photochromic naphthopyrans |
| 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 |
| DE60106311T2 (de) * | 2000-03-02 | 2006-02-09 | Merck Patent Gmbh | Mehrschichtiger reflektierender Film oder Pigment mit von Blickwinkel abhängigen Reflektionseigenschaften |
| EP1170353B1 (en) | 2000-07-06 | 2005-11-02 | Fuji Photo Film Co., Ltd. | Liquid crystal composition comprising liquid crystal molecules and aligment promoter |
| FR2811322B1 (fr) | 2000-07-07 | 2002-10-18 | Essilor Int | Procede de preparation d'un latex de polyurethane photochromique et application a l'optique ophtalmique |
| US6599973B1 (en) * | 2000-09-27 | 2003-07-29 | E. I. Du Pont De Nemours And Company | Aqueous graft copolymer pigment dispersants |
| US6645767B1 (en) * | 2000-10-03 | 2003-11-11 | Carnegie Mellon University | Cells engineered to contain genes of interest without expressed bacterial sequences and materials and methods therefor |
| FR2816950B1 (fr) | 2000-11-17 | 2003-02-14 | Essilor Int | Procede d'obtention d'un latex photochromique |
| US6433043B1 (en) * | 2000-11-28 | 2002-08-13 | Transitions Optical, Inc. | Removable imbibition composition of photochromic compound and kinetic enhancing additive |
| WO2002057070A2 (en) | 2000-11-29 | 2002-07-25 | Zms, Llc | Photochromic articles and methods for making them |
| US6764710B2 (en) | 2001-07-18 | 2004-07-20 | Scimed Life Systems, Inc. | Light emitting markers for use with substrates |
| US6525136B1 (en) * | 2001-08-02 | 2003-02-25 | Xerox Corporation | Photochromic core and shell matrix |
| KR100482654B1 (ko) | 2001-09-18 | 2005-04-13 | 한국화학연구원 | 광변색 나노 캡슐 및 그의 제조방법 |
| US6998072B2 (en) | 2001-11-01 | 2006-02-14 | Transitions Optical, Inc. | Photochromic polymerizable compositions |
| US20030141490A1 (en) * | 2001-12-21 | 2003-07-31 | Walters Robert W. | Photochromic polymer compositions and articles thereof |
| US7452611B2 (en) | 2001-12-27 | 2008-11-18 | Transitions Optical, Inc. | Photochromic optical article |
| US6986471B1 (en) * | 2002-01-08 | 2006-01-17 | Flame Spray Industries, Inc. | Rotary plasma spray method and apparatus for applying a coating utilizing particle kinetics |
| TW594946B (en) | 2002-01-16 | 2004-06-21 | Sanken Electric Co Ltd | Manufacturing method of semiconductor device |
| US20030174560A1 (en) | 2002-02-26 | 2003-09-18 | Klaus-Hermann Dahmen | Photochromic compounds for molecular switches and optical memory |
| US7163769B2 (en) | 2002-03-11 | 2007-01-16 | Pavel Cheben | Photosensitive material and process of making same |
| US6687266B1 (en) * | 2002-11-08 | 2004-02-03 | Universal Display Corporation | Organic light emitting materials and devices |
| US20050042758A1 (en) * | 2003-08-20 | 2005-02-24 | Honeywell Corporation | Leak detection method using microencapsulated dye precursor |
| US7261843B2 (en) * | 2004-03-04 | 2007-08-28 | Transitions Optical, Inc. | Photochromic optical article |
-
2004
- 2004-07-16 US US10/892,919 patent/US8153344B2/en active Active
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2005
- 2005-04-21 WO PCT/US2005/013803 patent/WO2006019435A1/en active Application Filing
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2013
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| HK1105155A1 (en) | 2008-02-01 |
| JP2008506031A (ja) | 2008-02-28 |
| KR20070046115A (ko) | 2007-05-02 |
| BRPI0513420A (pt) | 2008-05-06 |
| CN101735795A (zh) | 2010-06-16 |
| JP5470207B2 (ja) | 2014-04-16 |
| KR20090113387A (ko) | 2009-10-30 |
| JP5372370B2 (ja) | 2013-12-18 |
| JP2011006704A (ja) | 2011-01-13 |
| US8153344B2 (en) | 2012-04-10 |
| CN101735795B (zh) | 2014-06-11 |
| CN103955116A (zh) | 2014-07-30 |
| AU2005272981A1 (en) | 2006-02-23 |
| KR100939396B1 (ko) | 2010-01-28 |
| HK1140787A1 (zh) | 2010-10-22 |
| MX2007000522A (es) | 2007-03-07 |
| WO2006019435A1 (en) | 2006-02-23 |
| JP2014065910A (ja) | 2014-04-17 |
| CA2573595A1 (en) | 2006-02-23 |
| CN101006156A (zh) | 2007-07-25 |
| EP1778815A1 (en) | 2007-05-02 |
| CN101006156B (zh) | 2011-01-19 |
| EP1778815B1 (en) | 2011-12-14 |
| ES2377215T3 (es) | 2012-03-23 |
| CN103955116B (zh) | 2017-11-17 |
| AU2005272981B2 (en) | 2009-04-30 |
| CA2573595C (en) | 2012-01-24 |
| US20060014099A1 (en) | 2006-01-19 |
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