TW467932B - Benzotriazole UV absorbers having enhanced durability - Google Patents
Benzotriazole UV absorbers having enhanced durability Download PDFInfo
- Publication number
- TW467932B TW467932B TW086117258A TW86117258A TW467932B TW 467932 B TW467932 B TW 467932B TW 086117258 A TW086117258 A TW 086117258A TW 86117258 A TW86117258 A TW 86117258A TW 467932 B TW467932 B TW 467932B
- Authority
- TW
- Taiwan
- Prior art keywords
- tert
- butyl
- benzotriazole
- carbon atoms
- group
- Prior art date
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- 239000012964 benzotriazole Substances 0.000 title claims abstract description 53
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 239000006096 absorbing agent Substances 0.000 title abstract description 20
- -1 acrylic polyol Chemical class 0.000 claims abstract description 201
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 101
- 239000000203 mixture Substances 0.000 claims abstract description 87
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 85
- 239000001257 hydrogen Substances 0.000 claims abstract description 61
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 61
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 59
- 238000000576 coating method Methods 0.000 claims abstract description 45
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 239000011347 resin Substances 0.000 claims abstract description 36
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000011248 coating agent Substances 0.000 claims abstract description 30
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 28
- 125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 23
- 239000007787 solid Substances 0.000 claims abstract description 20
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 13
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 13
- 239000004640 Melamine resin Substances 0.000 claims abstract description 13
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 11
- 239000008199 coating composition Substances 0.000 claims abstract description 10
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 9
- 239000004593 Epoxy Substances 0.000 claims abstract description 8
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910000077 silane Inorganic materials 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims description 102
- 238000011049 filling Methods 0.000 claims description 72
- 230000002079 cooperative effect Effects 0.000 claims description 44
- 239000002253 acid Substances 0.000 claims description 31
- 150000002431 hydrogen Chemical class 0.000 claims description 27
- 229910052757 nitrogen Inorganic materials 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 22
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
- 239000000047 product Substances 0.000 claims description 21
- 150000001412 amines Chemical class 0.000 claims description 20
- 238000010521 absorption reaction Methods 0.000 claims description 19
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 18
- 229910052740 iodine Inorganic materials 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 150000007857 hydrazones Chemical class 0.000 claims description 11
- 150000003254 radicals Chemical class 0.000 claims description 11
- 239000007983 Tris buffer Substances 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 238000006068 polycondensation reaction Methods 0.000 claims description 9
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 9
- 150000001565 benzotriazoles Chemical class 0.000 claims description 8
- 239000007789 gas Substances 0.000 claims description 8
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
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- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 5
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 4
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- 239000002530 phenolic antioxidant Substances 0.000 claims description 3
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims description 2
- SFWOJBVSOFXBFK-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-octoxy-3H-pyridin-4-ol Chemical compound C(CCCCCCC)ON1C(CC(=CC1(C)C)O)(C)C SFWOJBVSOFXBFK-UHFFFAOYSA-N 0.000 claims description 2
- KTNPVRSKFWZJEZ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-1-amine Chemical compound CC1(C)CCCC(C)(C)N1N KTNPVRSKFWZJEZ-UHFFFAOYSA-N 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- MFCKXJXHJKOXHM-UHFFFAOYSA-N [3,3,3-tris[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-dimethylpropyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical group CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(C)(C)C(OC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(OC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)OC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MFCKXJXHJKOXHM-UHFFFAOYSA-N 0.000 claims description 2
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- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 claims description 2
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- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-OUBTZVSYSA-N potassium-40 Chemical compound [40K] ZLMJMSJWJFRBEC-OUBTZVSYSA-N 0.000 description 1
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 125000005581 pyrene group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 235000015598 salt intake Nutrition 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 1
- JMHCCAYJTTWMCX-QWPJCUCISA-M sodium;(2s)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate;pentahydrate Chemical compound O.O.O.O.O.[Na+].IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 JMHCCAYJTTWMCX-QWPJCUCISA-M 0.000 description 1
- XHFLOLLMZOTPSM-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrate Chemical compound [OH-].[Na+].OC(O)=O XHFLOLLMZOTPSM-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 108010063973 teneurin-1 Proteins 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- CMWCOKOTCLFJOP-UHFFFAOYSA-N titanium(3+) Chemical compound [Ti+3] CMWCOKOTCLFJOP-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 description 1
- 229940036248 turpentine 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
- 150000003672 ureas Chemical class 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 229920006163 vinyl copolymer Polymers 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
- UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C09D5/32—Radiation-absorbing paints
-
- 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
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
- C07D249/20—Benzotriazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6518—Five-membered rings
- C07F9/65188—Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
-
- 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
- C08K5/3472—Five-membered rings
-
- 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
- C09D133/00—Coating compositions based on 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C09D161/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C09D161/28—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
-
- 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
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Hydrogenated Pyridines (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74514696A | 1996-11-07 | 1996-11-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW467932B true TW467932B (en) | 2001-12-11 |
Family
ID=24995448
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW086117258A TW467932B (en) | 1996-11-07 | 1997-11-19 | Benzotriazole UV absorbers having enhanced durability |
Country Status (20)
Country | Link |
---|---|
JP (1) | JP4126364B2 (fr) |
KR (1) | KR100488744B1 (fr) |
CN (1) | CN1091127C (fr) |
AT (1) | AT407642B (fr) |
AU (1) | AU727301B2 (fr) |
BE (1) | BE1011537A3 (fr) |
BR (1) | BR9705437A (fr) |
CA (1) | CA2220269A1 (fr) |
CH (1) | CH693032A5 (fr) |
DE (1) | DE19748658B4 (fr) |
DK (1) | DK126697A (fr) |
ES (1) | ES2134158B1 (fr) |
FR (1) | FR2755444B1 (fr) |
GB (1) | GB2319035B (fr) |
IT (1) | IT1298471B1 (fr) |
NL (1) | NL1007470C2 (fr) |
NO (1) | NO975104L (fr) |
SE (1) | SE522379C2 (fr) |
SG (1) | SG71056A1 (fr) |
TW (1) | TW467932B (fr) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6166218A (en) * | 1996-11-07 | 2000-12-26 | Ciba Specialty Chemicals Corporation | Benzotriazole UV absorbers having enhanced durability |
DE60003748T2 (de) * | 1999-04-23 | 2004-03-18 | Nippon Mitsubishi Oil Corp. | UV-absorbierende Harzzusammensetzung |
WO2000066676A1 (fr) * | 1999-05-03 | 2000-11-09 | Ciba Specialty Chemicals Holding Inc. | Compositions adhesives stabilisees contenant des absorbeurs d'u.v. a base de benzotriazole decalees vers le rouge tres solubles et photostables et articles stratifies fabriques avec ces compositions |
EP1232148B1 (fr) | 1999-11-16 | 2005-05-04 | Ciba SC Holding AG | Utilisation d'absorbeurs uv a base de benzotriazole |
WO2001057124A2 (fr) * | 2000-02-01 | 2001-08-09 | Ciba Specialty Chemicals Holding Inc. | Procede de protection de contenus grace a des agents d'absorptions des u.v. a efficacite durable |
US6489486B2 (en) * | 2000-02-21 | 2002-12-03 | Roche Vitamins Inc. | 2-hydroxyphenyl benzotriazoles as UV-A/B filters |
US6353113B1 (en) | 2000-08-03 | 2002-03-05 | Ciba Specialty Chemicals Corporation | Process for the preparation of 5-perfluoroalkyl substituted benzotriazole UV absorbers |
US6566507B2 (en) | 2000-08-03 | 2003-05-20 | Ciba Specialty Chemicals Corporation | Processes for the preparation of benzotriazole UV absorbers |
ES2232683T3 (es) * | 2000-11-27 | 2005-06-01 | Ciba Specialty Chemicals Holding Inc. | Derivados de 2-(2-hiddroxifenil)-2h-benzotriazoles, sustituidos en posicion 5 por arilo y en posicion 5 por heteroarilo, como absorbentes uv. |
US6649770B1 (en) | 2000-11-27 | 2003-11-18 | Ciba Specialty Chemicals Corporation | Substituted 5-aryl-2-(2-hydroxyphenyl)-2H-benzotriazole UV absorbers, compositions stabilized therewith and process for preparation thereof |
US6930136B2 (en) | 2001-09-28 | 2005-08-16 | National Starch And Chemical Investment Holding Corporation | Adhesion promoters containing benzotriazoles |
US7057264B2 (en) | 2002-10-18 | 2006-06-06 | National Starch And Chemical Investment Holding Corporation | Curable compounds containing reactive groups: triazine/isocyanurates, cyanate esters and blocked isocyanates |
JP2005320517A (ja) * | 2004-04-06 | 2005-11-17 | Matsushita Electric Works Ltd | 塗料組成物、塗膜付基材、照明器具及びランプ |
CN100455622C (zh) * | 2004-07-07 | 2009-01-28 | 株式会社艾迪科 | 氯乙烯类树脂组合物 |
EP2113536B1 (fr) | 2007-02-20 | 2012-07-04 | FUJIFILM Corporation | Utilisation de matière polymère contenant un absorbant d'ultraviolets |
JP2009067983A (ja) | 2007-03-30 | 2009-04-02 | Fujifilm Corp | 紫外線吸収剤組成物 |
US8039532B2 (en) | 2007-08-16 | 2011-10-18 | Fujifilm Corporation | Heterocyclic compound, ultraviolet absorbent and composition containing the same |
WO2009047982A1 (fr) * | 2007-10-10 | 2009-04-16 | Konica Minolta Opto, Inc. | Film de résine acrylique à usage optique, plaque de polarisation utilisant le film de résine acrylique à usage optique et dispositif d'affichage à cristaux liquides |
US20090214874A1 (en) * | 2008-02-27 | 2009-08-27 | Gm Global Technology Operations, Inc. | Enhanced coating or layer |
JP5428412B2 (ja) | 2008-03-18 | 2014-02-26 | 株式会社リコー | 耐熱性向上剤及び可逆性感熱記録媒体 |
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 |
JP2009270062A (ja) | 2008-05-09 | 2009-11-19 | Fujifilm Corp | 紫外線吸収剤組成物 |
BR112012017559A2 (pt) * | 2010-01-15 | 2016-08-16 | Dsm Ip Assets Bv | 2-fenil-1,2,3-benzotriazóis para a absorbância de radiação uv |
CN102050823A (zh) * | 2010-10-27 | 2011-05-11 | 华东理工大学 | 新型光稳定剂-鸟嘌呤类似物的合成及表征 |
US9808675B2 (en) | 2012-09-13 | 2017-11-07 | Acushnet Company | Golf ball compositions |
US9227109B2 (en) * | 2012-09-13 | 2016-01-05 | Acushnet Company | Golf ball compositions |
JP6430964B2 (ja) | 2013-12-09 | 2018-11-28 | 株式会社Adeka | 塗装性を向上させた被塗装基材 |
TWI483987B (zh) * | 2014-03-10 | 2015-05-11 | Sino Japan Chemical Co Ltd | 液態反應型紫外線吸收劑及其製造方法與應用 |
EP4282922A3 (fr) * | 2014-08-05 | 2024-02-21 | Miyoshi Oil & Fat Co., Ltd. | Additif pour conférer une capacité d'absorption des ultraviolets et/ou un indice de réfraction élevé à la matrice, et élément en résine l'utilisant |
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CN107533242B (zh) * | 2015-04-30 | 2020-06-26 | 东海光学株式会社 | 塑料透镜 |
CN106316970A (zh) * | 2016-08-11 | 2017-01-11 | 重庆大学 | 一类具有超热稳定性的含双苯并三氮唑有机染料 |
US10035043B2 (en) | 2016-12-15 | 2018-07-31 | Acushnet Company | Golf ball incorporating highly crosslinked thermoset fluorescent microspheres and methods of making same |
US10252112B2 (en) | 2017-03-20 | 2019-04-09 | Acushnet Company | Golf ball composition |
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US10723732B2 (en) | 2017-06-30 | 2020-07-28 | Johnson & Johnson Vision Care, Inc. | Hydroxyphenyl phenanthrolines as polymerizable blockers of high energy light |
US10526296B2 (en) | 2017-06-30 | 2020-01-07 | Johnson & Johnson Vision Care, Inc. | Hydroxyphenyl naphthotriazoles as polymerizable blockers of high energy light |
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US11993037B1 (en) | 2018-03-02 | 2024-05-28 | Johnson & Johnson Vision Care, Inc. | Contact lens displaying improved vision attributes |
US10935695B2 (en) | 2018-03-02 | 2021-03-02 | Johnson & Johnson Vision Care, Inc. | Polymerizable absorbers of UV and high energy visible light |
CN108949008A (zh) * | 2018-08-09 | 2018-12-07 | 深圳市前海奇迹新材料有限公司 | 一种钢化玻璃水性uv底漆 |
US11958824B2 (en) | 2019-06-28 | 2024-04-16 | Johnson & Johnson Vision Care, Inc. | Photostable mimics of macular pigment |
CN110606984B (zh) * | 2019-07-29 | 2021-02-19 | 宿迁联盛科技股份有限公司 | 一种光稳定剂及其制备方法 |
CN111205510A (zh) * | 2020-02-13 | 2020-05-29 | 西安工业大学 | 双功能型紫外线吸收剂及其制备方法 |
CN111575097B (zh) * | 2020-06-15 | 2021-04-16 | 清华大学 | 具有光致变粘度的溶液及调控流体粘度的方法 |
CN112079787A (zh) * | 2020-08-27 | 2020-12-15 | 宿迁联盛科技股份有限公司 | 一种硝基重氮盐偶合衍生物的还原工艺 |
US11697048B2 (en) | 2021-08-12 | 2023-07-11 | Acushnet Company | Colored golf ball and method of making same |
CN116178866B (zh) * | 2023-03-08 | 2023-10-13 | 江苏奥天利新材料有限公司 | 一种具有遮阳带的无光学缺陷的pvb中间膜制作方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3742243A (en) * | 1971-09-27 | 1973-06-26 | Veeder Industries Inc | Pulse generator |
NL7503046A (nl) * | 1975-03-14 | 1976-09-16 | Philips Nv | Elektrische machine. |
US4226763A (en) * | 1978-06-26 | 1980-10-07 | Ciba-Geigy Corporation | 2-[2-Hydroxy-3,5-di-(.alpha.,α-dimethylbenzyl)-phenyl]-2H-benzotriazole and stabilized compositions |
DE3519901C2 (de) * | 1985-06-04 | 1995-02-16 | Papst Motoren Gmbh & Co Kg | Kollektorloser Gleichstrommotor |
US4868246A (en) * | 1987-08-12 | 1989-09-19 | Pennwalt Corporation | Polymer bound UV stabilizers |
JP2534521B2 (ja) * | 1987-11-18 | 1996-09-18 | 株式会社セコー技研 | 3相半導体電動機 |
DE59107052D1 (de) * | 1990-03-30 | 1996-01-25 | Ciba Geigy Ag | Lackzusammensetzungen |
US5278314A (en) * | 1991-02-12 | 1994-01-11 | Ciba-Geigy Corporation | 5-thio-substituted benzotriazole UV-absorbers |
US5280124A (en) * | 1991-02-12 | 1994-01-18 | Ciba-Geigy Corporation | 5-sulfonyl-substituted benzotriazole UV-absorbers |
CA2099154A1 (fr) * | 1992-09-24 | 1994-03-25 | Ronald E. Mac Leay | N-[2-hydroxy-3-(2h-benzotriazol-2-yl)benzyl]oxamides |
EP0590222A1 (fr) * | 1992-09-30 | 1994-04-06 | STMicroelectronics S.r.l. | Capteur de position magnétique |
US5292890A (en) * | 1993-05-05 | 1994-03-08 | Fairmount Chemical Company, Inc. | Asymmetrical benzotriazolylphenols |
EP0698637A3 (fr) * | 1994-08-22 | 1996-07-10 | Ciba Geigy Ag | Polyuréthanes stabilisés avec des absorbeurs d'UV sélectionnés de benzotriazole 5-substitués |
JPH08201490A (ja) * | 1995-01-31 | 1996-08-09 | Mitsumi Electric Co Ltd | センサic |
US5646088A (en) * | 1995-02-16 | 1997-07-08 | Ricoh Co., Ltd. | Thermosensitive recording material and production process thereof |
US5574166A (en) * | 1995-04-19 | 1996-11-12 | Ciba-Geigy Corporation | Crystalline form of 2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl)-2H-benzotriazole |
EP0750224A3 (fr) * | 1995-06-19 | 1997-01-08 | Eastman Kodak Company | Polymères absorbant l'UV à base de 2'-hydroxyphénylbenzotriazole avec des substituents particuliers et éléments photographiques les contenant |
JPH09163706A (ja) * | 1995-12-01 | 1997-06-20 | Sharp Corp | ホールic及びそれを用いたファンモータ |
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1997
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- 1997-11-04 FR FR9713829A patent/FR2755444B1/fr not_active Expired - Fee Related
- 1997-11-04 DE DE19748658.4A patent/DE19748658B4/de not_active Expired - Lifetime
- 1997-11-05 CA CA002220269A patent/CA2220269A1/fr not_active Abandoned
- 1997-11-05 NO NO975104A patent/NO975104L/no unknown
- 1997-11-05 ES ES009702293A patent/ES2134158B1/es not_active Expired - Fee Related
- 1997-11-05 GB GB9723303A patent/GB2319035B/en not_active Expired - Fee Related
- 1997-11-05 AU AU44360/97A patent/AU727301B2/en not_active Ceased
- 1997-11-06 AT AT0187497A patent/AT407642B/de not_active IP Right Cessation
- 1997-11-06 SG SG1997003966A patent/SG71056A1/en unknown
- 1997-11-06 BE BE9700892A patent/BE1011537A3/fr not_active IP Right Cessation
- 1997-11-06 BR BR9705437A patent/BR9705437A/pt not_active Application Discontinuation
- 1997-11-06 IT IT97MI002482A patent/IT1298471B1/it active IP Right Grant
- 1997-11-06 KR KR1019970058298A patent/KR100488744B1/ko not_active IP Right Cessation
- 1997-11-06 CN CN97122422A patent/CN1091127C/zh not_active Expired - Lifetime
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- 1997-11-07 DK DK199701266A patent/DK126697A/da not_active Application Discontinuation
- 1997-11-07 SE SE9704086A patent/SE522379C2/sv not_active IP Right Cessation
- 1997-11-19 TW TW086117258A patent/TW467932B/zh active
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