TWI476234B - Ｕｖ保護性組成物，製備這類組成物之方法，以其塗覆基材之方法及由其形成之多層物件 - Google Patents
Ｕｖ保護性組成物，製備這類組成物之方法，以其塗覆基材之方法及由其形成之多層物件 Download PDFInfo
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- TWI476234B TWI476234B TW097136559A TW97136559A TWI476234B TW I476234 B TWI476234 B TW I476234B TW 097136559 A TW097136559 A TW 097136559A TW 97136559 A TW97136559 A TW 97136559A TW I476234 B TWI476234 B TW I476234B
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- Prior art keywords
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- coating
- primer
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Links
- 239000000203 mixture Substances 0.000 title claims description 82
- 238000000034 method Methods 0.000 title claims description 43
- 238000000576 coating method Methods 0.000 title claims description 35
- 239000011248 coating agent Substances 0.000 title claims description 28
- 239000000758 substrate Substances 0.000 title claims description 15
- 230000001681 protective effect Effects 0.000 title description 2
- 239000007787 solid Substances 0.000 claims description 28
- 239000002904 solvent Substances 0.000 claims description 28
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 24
- 238000009472 formulation Methods 0.000 claims description 22
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 13
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 229920001169 thermoplastic Polymers 0.000 claims description 9
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 8
- 239000002318 adhesion promoter Substances 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 8
- -1 benzophenone benzophenone Phenol Chemical compound 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 5
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 5
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 4
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 claims description 4
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 238000003618 dip coating Methods 0.000 claims description 4
- 229920000058 polyacrylate Polymers 0.000 claims description 4
- 150000002923 oximes Chemical class 0.000 claims description 3
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims description 3
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 3
- 238000004528 spin coating Methods 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- JTZMHBIDDPPUKL-UHFFFAOYSA-N 4,6-diphenylbenzene-1,3-diol Chemical compound OC1=CC(O)=C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 JTZMHBIDDPPUKL-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 239000002987 primer (paints) Substances 0.000 description 49
- 239000003973 paint Substances 0.000 description 46
- 229920000515 polycarbonate Polymers 0.000 description 29
- 239000004417 polycarbonate Substances 0.000 description 29
- 239000006096 absorbing agent Substances 0.000 description 18
- TWCBCCIODCKPGX-UHFFFAOYSA-N octyl 2-[4-[4,6-bis(4-phenylphenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]propanoate Chemical compound OC1=CC(OC(C)C(=O)OCCCCCCCC)=CC=C1C1=NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)=NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)=N1 TWCBCCIODCKPGX-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 230000006750 UV protection Effects 0.000 description 14
- 238000001723 curing Methods 0.000 description 14
- 239000004615 ingredient Substances 0.000 description 12
- 230000008033 biological extinction Effects 0.000 description 11
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 230000006870 function Effects 0.000 description 7
- 239000013500 performance material Substances 0.000 description 7
- 238000010790 dilution Methods 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- 238000003556 assay Methods 0.000 description 5
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 4
- 238000011105 stabilization Methods 0.000 description 4
- 239000011550 stock solution Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 230000032798 delamination Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910052724 xenon Inorganic materials 0.000 description 3
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 230000008520 organization Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
- IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004262 Ethyl gallate Substances 0.000 description 1
- 229920001283 Polyalkylene terephthalate Polymers 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- VQNRMLCRMNVBBP-UHFFFAOYSA-N aniline;oxalic acid Chemical compound OC(=O)C(O)=O.NC1=CC=CC=C1 VQNRMLCRMNVBBP-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- VPNXDYRDSMKQQM-UHFFFAOYSA-N benzene-1,3-diol;diphenylmethanone Chemical compound OC1=CC=CC(O)=C1.C=1C=CC=CC=1C(=O)C1=CC=CC=C1 VPNXDYRDSMKQQM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 125000005447 octyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- DCNNGUNBSPGSCQ-UHFFFAOYSA-N propanedioic acid;propane-1,2-diol Chemical compound CC(O)CO.OC(=O)CC(O)=O DCNNGUNBSPGSCQ-UHFFFAOYSA-N 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/002—Priming paints
-
- 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
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/48—Stabilisers against degradation by oxygen, light or heat
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007050192A DE102007050192A1 (de) | 2007-10-20 | 2007-10-20 | Zusammensetzung mit UV-Schutz |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200932805A TW200932805A (en) | 2009-08-01 |
| TWI476234B true TWI476234B (zh) | 2015-03-11 |
Family
ID=40266007
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW097136559A TWI476234B (zh) | 2007-10-20 | 2008-09-24 | Ｕｖ保護性組成物，製備這類組成物之方法，以其塗覆基材之方法及由其形成之多層物件 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8722778B2 (OSRAM) |
| EP (1) | EP2203504B1 (OSRAM) |
| JP (1) | JP5357887B2 (OSRAM) |
| KR (1) | KR101568434B1 (OSRAM) |
| CN (1) | CN101827883B (OSRAM) |
| BR (1) | BRPI0817666A2 (OSRAM) |
| DE (1) | DE102007050192A1 (OSRAM) |
| ES (1) | ES2400409T3 (OSRAM) |
| MX (1) | MX2010003123A (OSRAM) |
| PL (1) | PL2203504T3 (OSRAM) |
| TW (1) | TWI476234B (OSRAM) |
| WO (1) | WO2009049904A1 (OSRAM) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009019493B4 (de) * | 2009-05-04 | 2013-02-07 | Bayer Materialscience Aktiengesellschaft | Polar lösliche UV-Absorber |
| DE102009020938A1 (de) | 2009-05-12 | 2010-11-18 | Bayer Materialscience Ag | Witterungsstabile Mehrschichtsysteme |
| US8216357B2 (en) * | 2009-09-25 | 2012-07-10 | General Electric Company | Protective coating compositions and devices |
| CN102686658B (zh) * | 2009-12-21 | 2014-08-20 | 拜耳知识产权有限责任公司 | 包括基底层、底漆层和耐刮擦层的多层体系 |
| EP2447236A1 (de) | 2010-10-12 | 2012-05-02 | Bayer MaterialScience AG | Spezielle UV-Absorber für härtbare UV-Schutz Beschichtungen |
| CA2760319C (en) | 2010-12-06 | 2018-10-16 | Valspar Corporation | Radiation curable composite coating composition useful to form protective coatings |
| WO2015091425A1 (de) * | 2013-12-19 | 2015-06-25 | Bayer Materialscience Ag | Mehrschichtaufbau aus polycarbonat und polycarbonatblends mit hoher optischer güte, hoher kratzbeständigkeit und witterungsfestigkeit |
| KR20180063212A (ko) * | 2015-09-29 | 2018-06-11 | 비전 이즈, 엘피 | Uv 및 고에너지 가시광선을 흡수하는 안과용 렌즈 |
| KR102239091B1 (ko) * | 2017-09-01 | 2021-04-09 | (주)엘지하우시스 | 투명 수지 적층체, 이를 제조하는 방법 및 이를 이용한 자동차용 외장재. |
| EP3620288A1 (de) | 2018-09-10 | 2020-03-11 | Covestro Deutschland AG | Dynamisch temperiertes folien-hinterspritzen |
| PT3883735T (pt) * | 2018-11-23 | 2023-11-15 | Basf Coatings Gmbh | Método automatizado para a moldagem por injeção de constituintes revestidos |
| WO2020104185A1 (de) * | 2018-11-23 | 2020-05-28 | Basf Coatings Gmbh | Manuelles verfahren zum spritzformen von beschichteten bauteilen |
| EP3815898A1 (de) * | 2019-10-28 | 2021-05-05 | Covestro Deutschland AG | Schichtenverbund aus polycarbonat und polycarbonatblend zur verbesserten lackierbarkeit |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW449607B (en) * | 1995-03-15 | 2001-08-11 | Ciba Sc Holding Ag | Bisphenyl-substituted triazines |
| US20070104956A1 (en) * | 2005-11-10 | 2007-05-10 | Exatec Llc | Polycarbonate system having enhanced weatherability and method of making same |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4373061A (en) | 1980-05-30 | 1983-02-08 | General Electric Company | Silicone coating for unprimed plastic substrate and coated articles |
| US4410594A (en) | 1981-04-10 | 1983-10-18 | General Electric Company | Ultraviolet radiation stabilized coated polycarbonate article |
| US5041313A (en) | 1990-05-11 | 1991-08-20 | General Electric Company | Method for making silicone hardcoat composites and primer compositions |
| US5391765A (en) | 1993-04-16 | 1995-02-21 | Bristol-Myers Squibb Company | Cholesterol lowering/antioxidant nitroxides |
| US5391795A (en) * | 1994-02-18 | 1995-02-21 | General Electric Company | Silylated agents useful for absorbing ultraviolet light |
| KR100421831B1 (ko) * | 1995-03-15 | 2004-07-01 | 시바 스페셜티 케미칼스 홀딩 인크. | 광안정화제로서유용한비페닐-치환트리아진 |
| US6255483B1 (en) | 1995-03-15 | 2001-07-03 | Ciba Specialty Chemicals Corporation | Biphenyl-substituted triazines |
| CH692739A5 (de) * | 1996-03-26 | 2002-10-15 | Ciba Sc Holding Ag | Polymerzusammensetzungen enthaltend 2-Hydroxyphenyl-1,3,5-triazine als UV-Absorber sowie neue 2-Hydroxyphenyl-1,3,5-triazine |
| DE19739781A1 (de) * | 1996-09-13 | 1998-03-19 | Ciba Geigy Ag | Hydroxyphenyltriazine |
| BE1012529A3 (fr) | 1996-09-13 | 2000-12-05 | Ciba Sc Holding Ag | Melange de triaryltriazines et son utilisation pour la stabilisation de materiaux organiques. |
| US6191199B1 (en) | 1999-05-03 | 2001-02-20 | Ciba Speciatly Chemicals Corporation | Stabilized adhesive compositions containing highly soluble, high extinction photostable hydroxyphenyl-s-triazine UV absorbers and laminated articles derived therefrom |
| CO5231248A1 (es) * | 2000-07-26 | 2002-12-27 | Ciba Sc Holding Ag | Articulos transparentes de polimero de baja consistencia |
| EP1308084A1 (en) | 2002-10-02 | 2003-05-07 | Ciba SC Holding AG | Synergistic UV absorber combination |
| CN1795182A (zh) * | 2003-05-27 | 2006-06-28 | 西巴特殊化学品控股有限公司 | 氨基芳基－1,3,5－三嗪及其作为紫外吸收剂的应用 |
| DE102005017023A1 (de) * | 2005-04-13 | 2006-10-19 | Bayer Materialscience Ag | UV-stabilisierte Polycarbonatformkörper |
| DE102006016642A1 (de) * | 2006-04-08 | 2007-10-18 | Bayer Materialscience Ag | UV-härtende Schutzschicht für thermoplastische Substrate |
-
2007
- 2007-10-20 DE DE102007050192A patent/DE102007050192A1/de not_active Withdrawn
-
2008
- 2008-09-24 TW TW097136559A patent/TWI476234B/zh active
- 2008-10-18 KR KR1020107008470A patent/KR101568434B1/ko active Active
- 2008-10-18 BR BRPI0817666 patent/BRPI0817666A2/pt active IP Right Grant
- 2008-10-18 PL PL08840336T patent/PL2203504T3/pl unknown
- 2008-10-18 CN CN2008801121665A patent/CN101827883B/zh active Active
- 2008-10-18 ES ES08840336T patent/ES2400409T3/es active Active
- 2008-10-18 EP EP08840336A patent/EP2203504B1/de active Active
- 2008-10-18 JP JP2010529297A patent/JP5357887B2/ja active Active
- 2008-10-18 MX MX2010003123A patent/MX2010003123A/es active IP Right Grant
- 2008-10-18 WO PCT/EP2008/008834 patent/WO2009049904A1/de not_active Ceased
- 2008-10-20 US US12/254,387 patent/US8722778B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW449607B (en) * | 1995-03-15 | 2001-08-11 | Ciba Sc Holding Ag | Bisphenyl-substituted triazines |
| US20070104956A1 (en) * | 2005-11-10 | 2007-05-10 | Exatec Llc | Polycarbonate system having enhanced weatherability and method of making same |
Also Published As
| Publication number | Publication date |
|---|---|
| PL2203504T3 (pl) | 2013-06-28 |
| JP5357887B2 (ja) | 2013-12-04 |
| US20090130489A1 (en) | 2009-05-21 |
| ES2400409T3 (es) | 2013-04-09 |
| CN101827883B (zh) | 2013-07-24 |
| BRPI0817666A2 (pt) | 2015-03-31 |
| CN101827883A (zh) | 2010-09-08 |
| EP2203504B1 (de) | 2013-01-16 |
| EP2203504A1 (de) | 2010-07-07 |
| MX2010003123A (es) | 2010-04-07 |
| KR101568434B1 (ko) | 2015-11-11 |
| US8722778B2 (en) | 2014-05-13 |
| WO2009049904A1 (de) | 2009-04-23 |
| KR20100085046A (ko) | 2010-07-28 |
| TW200932805A (en) | 2009-08-01 |
| DE102007050192A1 (de) | 2009-04-23 |
| JP2011500905A (ja) | 2011-01-06 |
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