TWI330650B - Synergistic uv absorber combination - Google Patents
Synergistic uv absorber combination Download PDFInfo
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- TWI330650B TWI330650B TW092127182A TW92127182A TWI330650B TW I330650 B TWI330650 B TW I330650B TW 092127182 A TW092127182 A TW 092127182A TW 92127182 A TW92127182 A TW 92127182A TW I330650 B TWI330650 B TW I330650B
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- 239000006096 absorbing agent Substances 0.000 title claims description 37
- 230000002195 synergetic effect Effects 0.000 title 1
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- 239000003381 stabilizer Substances 0.000 claims abstract description 78
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- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims abstract 2
- -1 2-hydroxyphenyl Chemical group 0.000 claims description 229
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- 239000001257 hydrogen Substances 0.000 claims description 50
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- 125000000217 alkyl group Chemical group 0.000 claims description 43
- 239000000126 substance Substances 0.000 claims description 39
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- 239000012964 benzotriazole Substances 0.000 claims description 29
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
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- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical group C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 17
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- XWVHBWQEYOROBE-UHFFFAOYSA-N tridec-2-ene Chemical group CCCCCCCCCCC=CC XWVHBWQEYOROBE-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- 150000003648 triterpenes Chemical class 0.000 description 1
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 1
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 210000001635 urinary tract Anatomy 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
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- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
-
- 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
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/12—Aldehydes; Ketones
- D06M13/127—Mono-aldehydes, e.g. formaldehyde; Monoketones
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/352—Heterocyclic compounds having five-membered heterocyclic rings
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
- D06M13/358—Triazines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/18—Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/20—Polyalkenes, polymers or copolymers of compounds with alkenyl groups bonded to aromatic groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/25—Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/30—Flame or heat resistance, fire retardancy properties
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Textile Engineering (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Pharmacology & Pharmacy (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Paints Or Removers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Dental Preparations (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Cosmetics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405852A EP1308084A1 (en) | 2002-10-02 | 2002-10-02 | Synergistic UV absorber combination |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200422339A TW200422339A (en) | 2004-11-01 |
| TWI330650B true TWI330650B (en) | 2010-09-21 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW092127182A TWI330650B (en) | 2002-10-02 | 2003-10-01 | Synergistic uv absorber combination |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7332105B2 (enExample) |
| EP (2) | EP1308084A1 (enExample) |
| JP (2) | JP2006501339A (enExample) |
| KR (1) | KR100996586B1 (enExample) |
| CN (1) | CN1320049C (enExample) |
| AT (1) | ATE334168T1 (enExample) |
| AU (1) | AU2003293316B2 (enExample) |
| BR (1) | BR0314863B1 (enExample) |
| CA (1) | CA2495777C (enExample) |
| DE (1) | DE60307122T2 (enExample) |
| MX (1) | MXPA05002809A (enExample) |
| RU (1) | RU2337113C2 (enExample) |
| TW (1) | TWI330650B (enExample) |
| WO (1) | WO2004031294A1 (enExample) |
| ZA (1) | ZA200500955B (enExample) |
Families Citing this family (161)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US6899866B2 (en) | 2002-09-06 | 2005-05-31 | Cph Innovations Corporation | Photostabilization of a sunscreen composition with a combination of an α-cyano-β, β-diphenylacrylate compound and a dialkyl naphithalate |
| US6919473B2 (en) | 2002-09-17 | 2005-07-19 | Cph Innovations Corporation | Photostabilizers, UV absorbers, and methods of photostabilizing a sunscreen composition |
| US7544350B2 (en) | 2002-11-22 | 2009-06-09 | Hallstar Innovations Corp. | Method of decreasing the UV light degradation of polymers |
| US6824936B1 (en) * | 2003-08-05 | 2004-11-30 | Eastman Kodak Company | Hindered amine light stabilizer for improved yellow dark stability |
| EP1654726B1 (de) * | 2003-08-11 | 2010-04-28 | Valeo Schalter und Sensoren GmbH | Sensor für ein nahbereichserkennungs- bzw. einparkhilfesystem eines fahrzeugs und herstellungsverfahren hierfür |
| US7534420B2 (en) | 2004-02-25 | 2009-05-19 | Hallstar Innovations Corp. | Compounds derived from polyanhydride resins with film-forming, UV-absorbing, and photostablizing properties, compositions containing same, and methods of using the same |
| US7235587B2 (en) | 2004-07-01 | 2007-06-26 | Cph Innovations Corporation | Diesters containing two crylene or fluorene moieties, sunscreen compositions containing the same, and methods of photostabilizing a sunscreen compositions containing the same |
| DE102005012056A1 (de) | 2005-03-16 | 2006-09-28 | Basf Coatings Ag | Mehrschichtlackierungen, Verfahren zu ihrer Herstellung und deren Verwendung im Automobilbau |
| JP5034205B2 (ja) * | 2005-03-31 | 2012-09-26 | 大日本印刷株式会社 | 化粧シート |
| JP4800726B2 (ja) * | 2005-03-31 | 2011-10-26 | 大日本印刷株式会社 | 耐候剤組成物 |
| US8158678B2 (en) | 2005-04-07 | 2012-04-17 | Cph Innovations Corp. | Photoabsorbing, highly conjugated compounds of cyanoacrylic esters, sunscreen compositions and methods of use |
| DE102005017023A1 (de) | 2005-04-13 | 2006-10-19 | Bayer Materialscience Ag | UV-stabilisierte Polycarbonatformkörper |
| GB0515602D0 (en) | 2005-07-29 | 2005-09-07 | Great Lakes Chemical Europ | Colour stabilised polyolefins |
| DE102005041952A1 (de) * | 2005-09-03 | 2007-03-08 | Bayer Materialscience Ag | Zusammensetzungen enthaltend Polycarbonat und neuartige UV-Absorber |
| JP2007231060A (ja) * | 2006-02-28 | 2007-09-13 | Shin Etsu Chem Co Ltd | 硬化性組成物及び被覆物品 |
| DE102006016642A1 (de) * | 2006-04-08 | 2007-10-18 | Bayer Materialscience Ag | UV-härtende Schutzschicht für thermoplastische Substrate |
| TWI464201B (zh) * | 2006-12-19 | 2014-12-11 | Mitsubishi Polyester Film Gmbh | 單一或多層穩定的聚酯膜 |
| PL2104716T3 (pl) * | 2007-01-15 | 2018-07-31 | Basf Se | Podbarwione przezroczyste powłoki uv stabilizowane 2-hydroksyfenylotriazyną |
| DE102007011069A1 (de) * | 2007-03-07 | 2008-09-11 | Bayer Materialscience Ag | Polycarbonatzusammensetzung enthaltend UV-Absorber |
| DE102007011070A1 (de) | 2007-03-07 | 2008-09-11 | Bayer Materialscience Ag | Erzeugnis mit verbesserter Lackhaftung |
| DE102007017936A1 (de) * | 2007-04-13 | 2008-10-16 | Bayer Materialscience Ag | Erzeugnisse mit verbesserter Flammwidrigkeit |
| JP5181558B2 (ja) * | 2007-07-13 | 2013-04-10 | コニカミノルタアドバンストレイヤー株式会社 | 光学フィルム、偏光板、及び液晶表示装置 |
| JP2010287310A (ja) * | 2007-10-12 | 2010-12-24 | Asahi Glass Co Ltd | 光学フィルタ |
| DE102007050192A1 (de) | 2007-10-20 | 2009-04-23 | Bayer Materialscience Ag | Zusammensetzung mit UV-Schutz |
| JP2009101603A (ja) * | 2007-10-23 | 2009-05-14 | Toppan Printing Co Ltd | 化粧シート |
| DE102007052783A1 (de) | 2007-11-02 | 2009-05-07 | Bayer Materialscience Ag | Flammwidrige Polycarbonate mit Polyolen |
| ATE544810T1 (de) * | 2007-12-21 | 2012-02-15 | Basf Se | Nanostrukturierte uv-absorber |
| JP5250289B2 (ja) * | 2008-03-31 | 2013-07-31 | 富士フイルム株式会社 | 紫外線吸収剤組成物 |
| JP5244437B2 (ja) * | 2008-03-31 | 2013-07-24 | 富士フイルム株式会社 | 紫外線吸収剤組成物 |
| KR20110020862A (ko) * | 2008-06-02 | 2011-03-03 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 접착성 캡슐화 조성물 및 그것을 사용하여 제조한 전자 소자 |
| MX2010013422A (es) * | 2008-06-27 | 2011-02-25 | Basf Se | Estabilizacion de productos para cuidado corporal y domesticos. |
| US20100104769A1 (en) * | 2008-10-23 | 2010-04-29 | Boisseau John E | Automotive coating surface enhancement using a plasma treatment technique |
| DE102008054329A1 (de) | 2008-11-03 | 2010-05-06 | Bayer Materialscience Ag | Erzeugnisse mit verbesserter Flammwidrigkeit |
| CN102292397B (zh) | 2009-01-19 | 2014-12-10 | 巴斯夫欧洲公司 | 有机黑色颜料及其制备 |
| TWI373671B (en) | 2009-02-26 | 2012-10-01 | Au Optronics Corp | Alighment material composition and alignment layer |
| DE102009020933A1 (de) | 2009-05-12 | 2010-11-18 | Bayer Materialscience Ag | Langzeit UV-stabile kälte schlagzähe Coextrusionsfolien |
| DE102009020938A1 (de) | 2009-05-12 | 2010-11-18 | Bayer Materialscience Ag | Witterungsstabile Mehrschichtsysteme |
| DE102009020934A1 (de) | 2009-05-12 | 2010-11-18 | Bayer Materialscience Ag | UV-härtende Schutzschicht für thermoplastische Substrate |
| CN102498164B (zh) | 2009-07-29 | 2015-08-19 | 拜尔材料科学股份公司 | 包括含丙烯酸酯涂层的多层产品 |
| EP2461955B1 (de) | 2009-08-03 | 2013-11-13 | Bayer Intellectual Property GmbH | Herstellung von additivierten formkörpern |
| CN101629034B (zh) * | 2009-08-03 | 2012-07-04 | 重庆大学 | 一种紫外吸收剂及其制备方法 |
| US20120145236A1 (en) | 2009-08-18 | 2012-06-14 | Basf Se | Uv-stabilized photovoltaic module |
| DE102009039121A1 (de) | 2009-08-28 | 2011-03-03 | Bayer Materialscience Ag | Erzeugnisse mit verbesserter Flammwidrigkeit |
| DE102009042307A1 (de) | 2009-09-19 | 2011-05-12 | Bayer Materialscience Ag | Kombination zweier Triazin UV Absorber für Lack auf PC |
| EP2480412B1 (de) | 2009-09-24 | 2017-07-05 | Covestro Deutschland AG | Spritzgegossene mehrkomponenten-verbundsysteme mit verbessertem brandverhalten |
| EP2312079A1 (de) | 2009-10-17 | 2011-04-20 | Bayer Sheet Europe GmbH | Stegplatte enthaltend expandierten Füllstoff |
| WO2011054865A2 (de) | 2009-11-05 | 2011-05-12 | Bayer Materialscience Ag | Polycarbonatzusammensetzung mit verbesserter flammwidrigkeit für extrusionsanwendungen |
| DE102009052042A1 (de) | 2009-11-05 | 2011-05-12 | Bayer Materialscience Ag | Polycarbonatzusammensetzung mit verbesserter Flammwidrigkeit für Extrusionsanwendungen |
| CN102666703B (zh) | 2009-11-05 | 2014-12-24 | 拜尔材料科学股份公司 | 具有改进的阻燃性的聚碳酸酯板 |
| DE102009052363A1 (de) | 2009-11-07 | 2011-05-12 | Bayer Materialscience Ag | Polycarbonate mit verbesserter Transmission |
| MX2012006323A (es) | 2009-12-05 | 2012-11-06 | Bayer Ip Gmbh | Composiciones de policarbonato con derivado de triazina sustituido fenolicamente. |
| DE102009058200A1 (de) | 2009-12-15 | 2011-06-16 | Bayer Materialscience Ag | Polymer-Zusammensetzung mit Wärme-absorbierenden Eigenschaften und hoher Stabilität |
| JP2013517364A (ja) | 2010-01-22 | 2013-05-16 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 高い透過率を備える防炎性の物品 |
| ITRM20100227A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento di calore ad alta stabilità. |
| ITRM20100226A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizioni stabilizzanti. |
| ITRM20100228A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
| ITRM20100225A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
| CN107260744A (zh) * | 2010-09-14 | 2017-10-20 | 巴斯夫欧洲公司 | 特殊二(联苯基)三嗪衍生物及其混合物作为uv吸收剂的用途 |
| EP2447236A1 (de) | 2010-10-12 | 2012-05-02 | Bayer MaterialScience AG | Spezielle UV-Absorber für härtbare UV-Schutz Beschichtungen |
| KR101920505B1 (ko) | 2010-10-25 | 2018-11-20 | 코베스트로 도이칠란드 아게 | 에너지 투과율이 낮은 다층 플라스틱 구조체 |
| DE102010042939A1 (de) | 2010-10-26 | 2012-04-26 | Bayer Materialscience Aktiengesellschaft | Fugenlose Heckklappe |
| KR101838994B1 (ko) | 2010-11-05 | 2018-03-15 | 코베스트로 도이칠란드 아게 | 분자량 분해가 낮은 내염성 uv-보호 폴리카보네이트 성형 조성물 |
| US20130221294A1 (en) | 2010-11-05 | 2013-08-29 | Bayer Intellectual Property Gmbh | Uv-protected polycarbonate molding materials equipped so as to be flame-retardant and having a low molecular weight decrease |
| WO2012069590A1 (de) | 2010-11-24 | 2012-05-31 | Bayer Materialscience Ag | Verfahren zur herstellung von optischen formkörpern |
| US11267951B2 (en) | 2010-12-13 | 2022-03-08 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| RU2597918C2 (ru) | 2010-12-13 | 2016-09-20 | Сайтек Текнолоджи Корп. | Технологические добавки и их применения в ротационном формовании |
| ITRM20100670A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Colorante organico e composizioni polimeriche colorate ad alta stabilità agli agenti atmosferici. |
| ITRM20100667A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento di calore ad alta stabilità agli agenti atmosferici. |
| IT1403380B1 (it) | 2010-12-17 | 2013-10-17 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento di calore ad alta stabilità agli agenti atmosferici. |
| ITRM20100668A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Substrato-led a colorazione stabile. |
| EP2468820A1 (en) | 2010-12-23 | 2012-06-27 | Bayer MaterialScience AG | Polycarbonate compositions with improved flame resistance |
| KR20140017541A (ko) * | 2011-01-31 | 2014-02-11 | 바스프 에스이 | 고온에서 가공된 폴리에틸렌을 난연 처리하는 방법 |
| EP2481847A1 (en) * | 2011-01-31 | 2012-08-01 | DSM IP Assets B.V. | UV-Stabilized high strength fiber |
| EP2543695A1 (de) | 2011-07-08 | 2013-01-09 | Bayer MaterialScience AG | Matte, flammgeschützte Artikel mit hoher Transmission |
| AU2012324995C1 (en) | 2011-10-18 | 2016-12-15 | Covestro Deutschland Ag | Polymer composition with heat-absorbing properties |
| BR112014012642A2 (pt) | 2011-11-30 | 2017-06-13 | Bayer Ip Gmbh | objetos de camada múltipla feitos de policarbonato com efeito de brilho intenso |
| BR112014012633A2 (pt) | 2011-11-30 | 2017-06-13 | Bayer Ip Gmbh | corpos multicamada feitos de policarbonato com um efeito brilho profundo |
| RU2485598C1 (ru) * | 2011-12-14 | 2013-06-20 | Государственное бюджетное образовательное учреждение высшего профессионального образования "Амурская государственная медицинская академия" Минздравсоцразвития Российской Федерации | Способ повышения неспецифической резистентности организма в условиях ультрафиолетового облучения |
| WO2013167542A1 (de) | 2012-05-08 | 2013-11-14 | Bayer Materialscience Gmbh | Lichtführungspiatte |
| UA119740C2 (uk) | 2012-06-13 | 2019-08-12 | Сайтек Текнолоджи Корп. | Композиції стабілізатора, що містять заміщені хроманові сполуки, і способи застосування |
| EP2700455A1 (de) | 2012-08-23 | 2014-02-26 | Bayer MaterialScience AG | Nasslackapplikation auf Kunststoffsubstraten mit Plasmahärtung |
| CN102851942A (zh) * | 2012-08-29 | 2013-01-02 | 昆山铁牛衬衫厂 | 防紫外线纯棉织物的整理方法 |
| CN104995247B (zh) | 2012-12-20 | 2018-05-08 | 科思创德国股份有限公司 | 有机着色剂和具有良好加工性质的着色聚合物组合物 |
| KR20150096734A (ko) | 2012-12-20 | 2015-08-25 | 바이엘 머티리얼사이언스 아게 | Ir-반사 안료를 함유하는 짙게 착색된 폴리카르보네이트 성형 컴파운드 |
| ITRM20120656A1 (it) | 2012-12-20 | 2014-06-21 | Bayer Materialscience Ag | Articolo multistrato a base di policarbonato con forte resistenza agli agenti atmosferici. |
| US9713915B2 (en) | 2013-01-18 | 2017-07-25 | Covestro Deutschland Ag | Bird protection glazing |
| WO2014118251A1 (de) | 2013-02-01 | 2014-08-07 | Bayer Materialscience Ag | Uv-härtbare beschichtungszusammensetzung |
| TW201434821A (zh) * | 2013-02-01 | 2014-09-16 | Bayer Materialscience Ag | 製造可聚合的ｕｖ吸收劑之方法 |
| CN104936948B (zh) | 2013-02-01 | 2018-11-27 | 科思创德国股份有限公司 | 包含uv吸收剂的氨基甲酸酯丙烯酸酯 |
| US9969864B2 (en) | 2013-07-08 | 2018-05-15 | Basf Se | Light stabilizers |
| TWI649354B (zh) | 2013-10-08 | 2019-02-01 | 科思創德意志股份有限公司 | 聚矽氧烷-聚碳酸酯嵌段共縮合物 |
| EP3055342A2 (en) | 2013-10-08 | 2016-08-17 | Covestro Deutschland AG | Process for preparing polysiloxane-polycarbonate block cocondensates using a salt of a weak acid |
| ES2751459T3 (es) | 2013-10-08 | 2020-03-31 | Covestro Deutschland Ag | Preparación de copolicarbonatos de bloques que contienen siloxano por medio de extrusión reactiva |
| JP6695272B2 (ja) | 2013-10-08 | 2020-05-20 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | ポリシロキサン−ポリカーボネートブロック共縮合物を調製する方法 |
| US11114648B2 (en) | 2014-01-21 | 2021-09-07 | Covestro Deutschland Ag | UV-protected component for OLEDs |
| EP2897186B1 (de) | 2014-01-21 | 2018-12-26 | Covestro Deutschland AG | UV-Schutzfolie für OLEDs |
| KR102270558B1 (ko) | 2014-01-30 | 2021-06-29 | 코베스트로 도이칠란트 아게 | 개선된 레올로지 특성을 갖는 폴리실록산-폴리카르보네이트 블록 공축합물 |
| JP6821555B2 (ja) * | 2014-09-09 | 2021-01-27 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | 化粧用ｕｖ吸収体混合物 |
| KR102391932B1 (ko) | 2014-09-11 | 2022-04-28 | 코베스트로 도이칠란트 아게 | 자동차 글레이징 시스템용 트림 |
| CN105218857B (zh) * | 2014-09-25 | 2016-08-24 | 黄秀茹 | 一种用于聚合物的添加剂 |
| CN107207773A (zh) | 2014-11-20 | 2017-09-26 | 塞特工业公司 | 稳定剂组合物以及使用该稳定剂组合物保护有机材料免受uv光和热降解的方法 |
| EP3247742B1 (de) | 2015-01-20 | 2020-12-16 | Covestro Intellectual Property GmbH & Co. KG | Flammgeschützte formmassen enthaltend siloxan-haltiges polycarbonat-blockcokondensat |
| EP3247743B1 (de) | 2015-01-20 | 2020-10-07 | Covestro Intellectual Property GmbH & Co. KG | Flammgeschützte, glasfaser-haltige formmassen enthaltend siloxan-haltiges polycarbonat-blockcokondensat |
| CN107428926B (zh) | 2015-04-07 | 2021-02-09 | 科思创德国股份有限公司 | 聚硅氧烷和基于二羟基二苯基环烷烃的（共）聚碳酸酯的嵌段共缩合物 |
| JP2017047687A (ja) | 2015-09-04 | 2017-03-09 | 凸版印刷株式会社 | 化粧シート |
| CN105647267B (zh) * | 2016-04-12 | 2018-05-04 | 深圳市美芝装饰设计工程股份有限公司 | 一种建筑室内用腻子 |
| KR20190014544A (ko) | 2016-06-03 | 2019-02-12 | 코베스트로 도이칠란트 아게 | 특정한 코폴리카르보네이트를 매트릭스 재료로서 함유하는 다층 복합 재료 |
| EP3519217B1 (de) | 2016-09-27 | 2021-06-30 | Covestro Intellectual Property GmbH & Co. KG | Kraftfahrzeug, aufweisend zwei a-säulen und eine frontscheibe |
| KR102415540B1 (ko) | 2016-11-17 | 2022-07-04 | 코베스트로 도이칠란트 아게 | 열 관리를 위한 투명한 다층 구조체 |
| KR102437318B1 (ko) | 2016-11-17 | 2022-08-31 | 코베스트로 도이칠란트 아게 | 열 관리를 위한 폴리카르보네이트의 불투명한 다층체 |
| ES2906904T3 (es) * | 2016-11-29 | 2022-04-20 | Toppan Printing Co Ltd | Lámina cosmética y método para producir una lámina cosmética |
| EP3554722A1 (de) | 2016-12-15 | 2019-10-23 | Covestro Deutschland AG | Transparent beschichtetes polycarbonat bauteil, dessen herstellung und verwendung |
| JP2020502342A (ja) | 2016-12-19 | 2020-01-23 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | 相溶化剤を用いたシロキサン含有ブロックコポリカーボネートの製造 |
| JP7110606B2 (ja) * | 2017-02-27 | 2022-08-02 | 東ソー株式会社 | 熱可塑性ポリウレタン樹脂組成物、および該樹脂組成物を用いた成形体 |
| EP3593363B1 (en) | 2017-03-10 | 2025-09-03 | AdvanSix Resins & Chemicals LLC | Wire and cable jacket composition of pa6/66 copolymer base resin for improved processability and properties |
| EP3395875B2 (de) | 2017-04-24 | 2023-01-25 | Covestro Deutschland AG | Laserstrahl-durchlässiges substratmaterial für sensoranwendungen |
| CN110352223B (zh) * | 2017-04-25 | 2022-08-02 | 巴斯夫欧洲公司 | 具有共价结合紫外线吸收剂的涂料组合物 |
| US11598495B2 (en) | 2017-07-24 | 2023-03-07 | Covestro Deutschland Ag | LED lighting elements comprising molded parts made of translucent polycarbonate compositions having a deep gloss effect |
| KR102020855B1 (ko) * | 2017-08-04 | 2019-09-16 | 주식회사 솔루트 | 자외선 차단 필름 |
| GB2567456B (en) * | 2017-10-12 | 2021-08-11 | Si Group Switzerland Chaa Gmbh | Antidegradant blend |
| CN111448473B (zh) | 2017-12-21 | 2024-12-03 | 科思创德国股份有限公司 | 包括多层体和lidar传感器的装置 |
| EP3578599A1 (en) | 2018-06-08 | 2019-12-11 | Cytec Industries Inc. | Granular stabilizer compositions for use in polymer resins and methods of making same |
| BR112020021798B1 (pt) * | 2018-04-27 | 2023-10-31 | Dow Global Technologies Llc | Composição e condutor revestido |
| JP2021531995A (ja) | 2018-05-29 | 2021-11-25 | コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー | 高い耐候安定性を有する、ポリカーボネート製の不透明多層体 |
| CN111073119A (zh) * | 2018-10-18 | 2020-04-28 | 中国石油化工股份有限公司 | 助剂组合物和线性中密度聚乙烯组合物及其制备方法以及聚乙烯滚塑制品 |
| WO2023025705A1 (en) | 2018-12-05 | 2023-03-02 | Covestro Deutschland Ag | A multilayer composite sheet for antenna housing |
| EP4140729B1 (en) | 2021-08-26 | 2024-05-01 | Covestro Deutschland AG | A multilayer composite sheet for antenna housing |
| US11958994B2 (en) * | 2019-03-29 | 2024-04-16 | Dai Nippon Printing Co., Ltd. | Sheet, ornamental material, and resin composition |
| AU2020251539B2 (en) * | 2019-03-29 | 2023-03-30 | Dai Nippon Printing Co., Ltd. | Cosmetic sheet and cosmetic material using same, and resin composition for surface protection layer |
| EP3719077B1 (de) | 2019-04-02 | 2022-09-21 | Covestro Deutschland AG | Siloxan-haltige blockcopolycarbonate mit geringer domänengrösse |
| US20220259410A1 (en) * | 2019-07-10 | 2022-08-18 | Clariant International Ltd | Stabilizer composition for silyl-modified polymer sealants |
| EP3778747A1 (en) * | 2019-08-14 | 2021-02-17 | Borealis AG | Uv stabilization of a cross-linkable polyolefin composition comprising an acidic silanol condensation catalyst |
| EP4023439B1 (en) | 2019-08-26 | 2024-09-18 | Denka Company Limited | Vinylidene fluoride resin multilayer film, automobile interior/exterior film, automobile component, and automobile |
| DE202020101945U1 (de) | 2019-09-30 | 2021-01-15 | Covestro Deutschland Ag | LED-Beleuchtungselemente auf Basis von Mehrschichtkörpern mit Massivsteinoptik |
| DE202020101944U1 (de) | 2019-09-30 | 2021-01-15 | Covestro Deutschland Ag | LED-Beleuchtungselemente auf Basis von Mehrschichtkörpern mit Steinoptik |
| EP3808819A1 (de) | 2019-10-15 | 2021-04-21 | Clariant International Ltd | Helle reiskleiewachsoxidate mit einem hohen esteranteil |
| FI4045597T3 (fi) | 2019-10-15 | 2024-03-18 | Clariant Int Ltd | Alhaisen happamuuden riisilesevahan oksidaatteja |
| EP3808818A1 (de) | 2019-10-15 | 2021-04-21 | Clariant International Ltd | Teilverseifte reiskleiewachsoxidate |
| WO2021076561A1 (en) | 2019-10-15 | 2021-04-22 | Covestro Llc | Three part headlamp assembly |
| WO2021148352A1 (en) * | 2020-01-21 | 2021-07-29 | Sabic Global Technologies B.V. | Pipe for transport of water containing chlorinated disinfectant |
| TR202001552A2 (tr) * | 2020-02-03 | 2021-08-23 | Aksa Akrilik Kimya Sanayii Anonim Sirketi | Güneş ışığına karşı stabilize edilmiş akrilik ve modakrilik elyaf |
| CN111393822B (zh) * | 2020-04-15 | 2022-05-31 | 佛山市汉纬新材料有限公司 | 一种壳体材料用pc/abs合金塑料及其制备方法 |
| US12486375B2 (en) | 2020-04-15 | 2025-12-02 | Covestro Deutschland Ag | Polycarbonate composite article |
| US20230167296A1 (en) | 2020-05-22 | 2023-06-01 | Covestro Deutschland Ag | Flame-retardant polycarbonate composition |
| CN115551945B (zh) | 2020-05-22 | 2025-10-28 | 科思创德国股份有限公司 | 阻燃聚碳酸酯组合物 |
| CN116057123A (zh) * | 2020-09-07 | 2023-05-02 | 陶氏环球技术有限责任公司 | 紫外线稳定的聚合物组合物 |
| WO2022148727A1 (en) * | 2021-01-05 | 2022-07-14 | Basf Se | Stabilizing a shaped polymer article against degradation induced by artificial uv-c light |
| CN115612213B (zh) * | 2021-07-12 | 2024-03-01 | 合肥杰事杰新材料股份有限公司 | 一种耐候聚丙烯复合材料及其制备方法和应用 |
| CN115612254B (zh) * | 2021-07-12 | 2025-07-11 | 合肥杰事杰新材料股份有限公司 | 一种耐候环氧树脂复合材料及其制备方法 |
| CN115612052B (zh) * | 2021-07-12 | 2024-10-25 | 合肥杰事杰新材料股份有限公司 | 一种具有高耐候性能的聚氨酯复合材料及其制备方法 |
| KR20240038007A (ko) * | 2021-07-17 | 2024-03-22 | 바스프 에스이 | 유기 물질의 안정화를 위한 첨가제 혼합물 |
| EP4140728A1 (en) | 2021-08-26 | 2023-03-01 | Covestro Deutschland AG | A multilayer composite sheet for antenna housing |
| EP4402204A1 (en) * | 2021-09-14 | 2024-07-24 | INEOS Styrolution Group GmbH | High clarity and low haze uv stabilized styrene and methyl methacrylate copolymers |
| AU2022346816A1 (en) * | 2021-09-16 | 2024-03-28 | Basf Se | Stabilizer formulation |
| CN114075360B (zh) * | 2022-01-10 | 2022-03-25 | 潍坊潍星联合橡塑有限公司 | 氯化聚乙烯混炼胶及其制备方法 |
| CN114591172B (zh) * | 2022-03-30 | 2023-11-10 | 上海金发科技发展有限公司 | 一种二十二酸二羟甲基丙酸酯化合物及其制备方法与应用 |
| CN114732750B (zh) * | 2022-04-21 | 2023-03-24 | 北京化工大学 | 一种氢化钛用于消除羟基自由基的用途及防晒抗老产品 |
| KR20250016214A (ko) * | 2022-05-24 | 2025-02-03 | 바스프 에스이 | 히드록시페닐 트리아진 및 uv 흡수제의 조합을 함유하는 폴리카르보네이트 조성물 |
| WO2025056330A1 (en) | 2023-09-13 | 2025-03-20 | Cytec Industries Inc. | Stabilized polymer compositions with improved color resistance |
| WO2025150156A1 (ja) * | 2024-01-11 | 2025-07-17 | 住友電気工業株式会社 | 樹脂組成物、電線、およびケーブル |
| CN119591966B (zh) * | 2025-02-10 | 2025-04-25 | 安徽紫金新材料科技股份有限公司 | 一种多层共挤的化妆品管材及其制备方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3535318A (en) * | 1967-03-13 | 1970-10-20 | American Cyanamid Co | Mono - aromatic - pentaalkyl ethers of hexamethylolmelamine crease-proofing agents |
| US5736597A (en) * | 1989-12-05 | 1998-04-07 | Ciba-Geigy Corporation | Stabilized organic material |
| JPH04257582A (ja) * | 1991-02-12 | 1992-09-11 | Fujisawa Pharmaceut Co Ltd | キノリジノン化合物またはその塩 |
| US5274015A (en) * | 1992-11-24 | 1993-12-28 | Phillips Petroleum Company | Compositions comprising sulfur-containing derivatives of hydroxyphenylbenzotriazole and process therefor |
| EP0711804A3 (de) * | 1994-11-14 | 1999-09-22 | Ciba SC Holding AG | Kryptolichtschutzmittel |
| US6255483B1 (en) * | 1995-03-15 | 2001-07-03 | Ciba Specialty Chemicals Corporation | Biphenyl-substituted triazines |
| FR2736390B1 (fr) * | 1995-07-05 | 1997-08-08 | Hispano Suiza Sa | Inverseur de poussee de turboreacteur a une coquille |
| US5962683A (en) | 1996-06-28 | 1999-10-05 | Ciba Specialty Chemicals Corp. | Oxazoline compounds as stabilizers |
| 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. |
| NZ502708A (en) * | 1997-08-20 | 2002-12-20 | Ciba Sc Holding Ag | Use of bis(resorcinyl)triazine derivatives (as sunscreens) for protecting human and animal skin and hair from the damaging effect of UV radiation |
| US5869554A (en) * | 1997-09-02 | 1999-02-09 | General Electric Company | Polycarbonate compositions comprising hindered amine light stabilizers and ultraviolet light absorbers |
| ZA9810599B (en) * | 1998-06-22 | 1999-07-30 | Cytec Tech Corp | Triazine UV absorber comprising amino resins. |
| US6218450B1 (en) * | 1999-12-13 | 2001-04-17 | Eastman Chemical Company | Copolyester containing isophthalic acid, 1,4-cyclohexanedimethanol, 4,4′-biphenyldicarboxylic acid and an ultraviolet light absorbing compound and articles made therefrom |
| US6352783B1 (en) * | 1999-12-13 | 2002-03-05 | Eastman Kodak Company | Copolyester containing 4,4'-biphenyldicarboxylic acid, 1,4-cyclohexanedimethanol and an ultraviolet light absorbing compound and articles made therefrom |
| MXPA02006120A (es) * | 1999-12-23 | 2002-12-05 | Ciba Sc Holding Ag | Mezcla de estabilizador. |
| JP2001262122A (ja) * | 2000-03-23 | 2001-09-26 | Sekisui Chem Co Ltd | 変成シリコーン系シーリング材組成物 |
| GB2361005B (en) * | 2000-04-04 | 2002-08-14 | Ciba Sc Holding Ag | Synergistic mixtures of uv-absorbers in polyolefins |
| US6297300B1 (en) * | 2000-05-19 | 2001-10-02 | The Dow Chemical Company | Carbonate polymer compositions comprising low volatile UV absorbers |
| DE60104313T2 (de) | 2000-05-19 | 2005-08-25 | Dow Global Technologies, Inc., Midland | Polycarbonatzusammensetzungen enthaltend schwerflüchtige uv-absorbierende verbindungen |
| CO5231248A1 (es) * | 2000-07-26 | 2002-12-27 | Ciba Sc Holding Ag | Articulos transparentes de polimero de baja consistencia |
| WO2002017873A1 (en) * | 2000-08-29 | 2002-03-07 | Ciba Specialty Chemicals Holding Inc. | Sunscreen compositions containing a dibenzoylmethane derivative and a triazine derivative |
| US20020167112A1 (en) * | 2001-02-06 | 2002-11-14 | Colburn Peter D. | Modified acrylic based compositions of enhanced optics and low temperature impact strength |
| TWI318208B (en) * | 2001-07-02 | 2009-12-11 | Ciba Sc Holding Ag | Highly compatible hydroxyphenyltriazine uv-absorbers |
| KR20040048959A (ko) * | 2001-10-18 | 2004-06-10 | 시바 스페셜티 케미칼스 홀딩 인크. | 유기 물질용 안정화제로서의 나프틸트리아진 |
| WO2003057772A2 (en) | 2001-12-27 | 2003-07-17 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
-
2002
- 2002-10-02 EP EP02405852A patent/EP1308084A1/en not_active Withdrawn
-
2003
- 2003-09-23 RU RU2005113718/04A patent/RU2337113C2/ru not_active IP Right Cessation
- 2003-09-23 CN CNB038234904A patent/CN1320049C/zh not_active Expired - Lifetime
- 2003-09-23 WO PCT/EP2003/010567 patent/WO2004031294A1/en not_active Ceased
- 2003-09-23 AU AU2003293316A patent/AU2003293316B2/en not_active Expired
- 2003-09-23 JP JP2004540677A patent/JP2006501339A/ja active Pending
- 2003-09-23 BR BRPI0314863-7B1A patent/BR0314863B1/pt not_active IP Right Cessation
- 2003-09-23 US US10/528,136 patent/US7332105B2/en not_active Expired - Lifetime
- 2003-09-23 AT AT03788915T patent/ATE334168T1/de not_active IP Right Cessation
- 2003-09-23 KR KR1020057005789A patent/KR100996586B1/ko not_active Expired - Lifetime
- 2003-09-23 MX MXPA05002809A patent/MXPA05002809A/es active IP Right Grant
- 2003-09-23 CA CA2495777A patent/CA2495777C/en not_active Expired - Lifetime
- 2003-09-23 EP EP03788915A patent/EP1549713B1/en not_active Expired - Lifetime
- 2003-09-23 DE DE60307122T patent/DE60307122T2/de not_active Expired - Lifetime
- 2003-10-01 TW TW092127182A patent/TWI330650B/zh not_active IP Right Cessation
-
2005
- 2005-02-02 ZA ZA200500955A patent/ZA200500955B/xx unknown
-
2010
- 2010-07-15 JP JP2010160157A patent/JP5405400B2/ja not_active Expired - Lifetime
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| EP1308084A1 (en) | 2003-05-07 |
| US7332105B2 (en) | 2008-02-19 |
| EP1549713A1 (en) | 2005-07-06 |
| EP1549713B1 (en) | 2006-07-26 |
| ATE334168T1 (de) | 2006-08-15 |
| AU2003293316A1 (en) | 2004-04-23 |
| RU2337113C2 (ru) | 2008-10-27 |
| US20060052491A1 (en) | 2006-03-09 |
| CN1320049C (zh) | 2007-06-06 |
| MXPA05002809A (es) | 2005-05-27 |
| TW200422339A (en) | 2004-11-01 |
| RU2005113718A (ru) | 2006-01-20 |
| AU2003293316B2 (en) | 2008-04-03 |
| WO2004031294A1 (en) | 2004-04-15 |
| KR20050073469A (ko) | 2005-07-13 |
| BR0314863A (pt) | 2005-08-02 |
| DE60307122D1 (de) | 2006-09-07 |
| DE60307122T2 (de) | 2006-11-30 |
| JP2010270336A (ja) | 2010-12-02 |
| BR0314863B1 (pt) | 2013-07-02 |
| JP5405400B2 (ja) | 2014-02-05 |
| JP2006501339A (ja) | 2006-01-12 |
| ZA200500955B (en) | 2006-03-29 |
| KR100996586B1 (ko) | 2010-11-25 |
| CA2495777A1 (en) | 2004-04-15 |
| CN1685008A (zh) | 2005-10-19 |
| CA2495777C (en) | 2012-11-13 |
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