ES2408171T3 - Producto de revestimiento con alta resistencia al rayado y estabilidad a la intemperie - Google Patents
Producto de revestimiento con alta resistencia al rayado y estabilidad a la intemperie Download PDFInfo
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- ES2408171T3 ES2408171T3 ES07856914T ES07856914T ES2408171T3 ES 2408171 T3 ES2408171 T3 ES 2408171T3 ES 07856914 T ES07856914 T ES 07856914T ES 07856914 T ES07856914 T ES 07856914T ES 2408171 T3 ES2408171 T3 ES 2408171T3
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- 238000000576 coating method Methods 0.000 title claims description 195
- 239000011248 coating agent Substances 0.000 title claims description 153
- 150000001875 compounds Chemical class 0.000 claims abstract description 71
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 24
- 238000004132 cross linking Methods 0.000 claims description 67
- 239000004922 lacquer Substances 0.000 claims description 59
- 239000005056 polyisocyanate Substances 0.000 claims description 57
- 229920001228 polyisocyanate Polymers 0.000 claims description 57
- -1 phosphoric acid diesters Chemical class 0.000 claims description 56
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 49
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 47
- 229920005862 polyol Polymers 0.000 claims description 45
- 150000003077 polyols Chemical class 0.000 claims description 45
- 239000003054 catalyst Substances 0.000 claims description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 31
- 150000001412 amines Chemical class 0.000 claims description 30
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 20
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 17
- 238000003860 storage Methods 0.000 claims description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000012948 isocyanate Substances 0.000 claims description 16
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- 238000005259 measurement Methods 0.000 claims description 13
- 125000000524 functional group Chemical group 0.000 claims description 11
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 10
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
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- 229910003813 NRa Inorganic materials 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
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- 229910002808 Si–O–Si Inorganic materials 0.000 claims description 8
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 6
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 6
- 239000011574 phosphorus Substances 0.000 claims description 6
- 125000004354 sulfur functional group Chemical group 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
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- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 238000002076 thermal analysis method Methods 0.000 claims description 5
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 4
- 239000000010 aprotic solvent Substances 0.000 claims description 4
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000013638 trimer Substances 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical class NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000000962 organic group Chemical group 0.000 claims description 3
- 229920000193 polymethacrylate Polymers 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims 1
- PAUHLEIGHAUFAK-UHFFFAOYSA-N 1-isocyanato-1-[(1-isocyanatocyclohexyl)methyl]cyclohexane Chemical compound C1CCCCC1(N=C=O)CC1(N=C=O)CCCCC1 PAUHLEIGHAUFAK-UHFFFAOYSA-N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000000470 constituent Substances 0.000 abstract description 6
- 239000008199 coating composition Substances 0.000 abstract 2
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 abstract 1
- 239000000047 product Substances 0.000 description 95
- 238000006243 chemical reaction Methods 0.000 description 42
- 229910000077 silane Inorganic materials 0.000 description 33
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 30
- 239000000203 mixture Substances 0.000 description 24
- 229920004482 WACKER® Polymers 0.000 description 23
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 21
- 150000004756 silanes Chemical class 0.000 description 20
- 238000012360 testing method Methods 0.000 description 17
- 238000002360 preparation method Methods 0.000 description 16
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- 239000007787 solid Substances 0.000 description 11
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- XCOASYLMDUQBHW-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OC)(OC)OC XCOASYLMDUQBHW-UHFFFAOYSA-N 0.000 description 9
- 238000002444 silanisation Methods 0.000 description 9
- 230000001588 bifunctional effect Effects 0.000 description 8
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- 238000003756 stirring Methods 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 7
- 238000004448 titration Methods 0.000 description 7
- TZZGHGKTHXIOMN-UHFFFAOYSA-N 3-trimethoxysilyl-n-(3-trimethoxysilylpropyl)propan-1-amine Chemical compound CO[Si](OC)(OC)CCCNCCC[Si](OC)(OC)OC TZZGHGKTHXIOMN-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 230000036961 partial effect Effects 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000005370 alkoxysilyl group Chemical group 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
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- 125000001424 substituent group Chemical group 0.000 description 4
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 3
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 150000008064 anhydrides Chemical class 0.000 description 3
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
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- 125000006850 spacer group Chemical group 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- KCZQSKKNAGZQSZ-UHFFFAOYSA-N 1,3,5-tris(6-isocyanatohexyl)-1,3,5-triazin-2,4,6-trione Chemical compound O=C=NCCCCCCN1C(=O)N(CCCCCCN=C=O)C(=O)N(CCCCCCN=C=O)C1=O KCZQSKKNAGZQSZ-UHFFFAOYSA-N 0.000 description 2
- BHWUCEATHBXPOV-UHFFFAOYSA-N 2-triethoxysilylethanamine Chemical compound CCO[Si](CCN)(OCC)OCC BHWUCEATHBXPOV-UHFFFAOYSA-N 0.000 description 2
- QHQNYHZHLAAHRW-UHFFFAOYSA-N 2-trimethoxysilylethanamine Chemical compound CO[Si](OC)(OC)CCN QHQNYHZHLAAHRW-UHFFFAOYSA-N 0.000 description 2
- FMGBDYLOANULLW-UHFFFAOYSA-N 3-isocyanatopropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCN=C=O FMGBDYLOANULLW-UHFFFAOYSA-N 0.000 description 2
- YATIYDNBFHEOFA-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-ol Chemical compound CO[Si](OC)(OC)CCCO YATIYDNBFHEOFA-UHFFFAOYSA-N 0.000 description 2
- SWDDLRSGGCWDPH-UHFFFAOYSA-N 4-triethoxysilylbutan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCCN SWDDLRSGGCWDPH-UHFFFAOYSA-N 0.000 description 2
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- 125000001931 aliphatic group Chemical group 0.000 description 2
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- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000006120 scratch resistant coating Substances 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- UZIAQVMNAXPCJQ-UHFFFAOYSA-N triethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)COC(=O)C(C)=C UZIAQVMNAXPCJQ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 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
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/625—Polymers of alpha-beta ethylenically unsaturated carboxylic acids; hydrolyzed polymers of esters of these acids
- C08G18/6254—Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/778—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8083—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/809—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006059951 | 2006-12-19 | ||
| DE102006059951 | 2006-12-19 | ||
| PCT/EP2007/011191 WO2008074490A1 (de) | 2006-12-19 | 2007-12-19 | Beschichtungsmittel mit hoher kratzbeständigkeit und witterungsstabilität |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2408171T3 true ES2408171T3 (es) | 2013-06-18 |
Family
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Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07856914T Active ES2408171T3 (es) | 2006-12-19 | 2007-12-19 | Producto de revestimiento con alta resistencia al rayado y estabilidad a la intemperie |
| ES07856915T Active ES2369110T3 (es) | 2006-12-19 | 2007-12-19 | Agente de revestimiento con alta resistencia al rayado y estabilidad a la intemperie. |
| ES07856913T Active ES2409182T3 (es) | 2006-12-19 | 2007-12-19 | Producto de revestimiento con alta resistencia al rayado y estabilidad a la intemperie |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07856915T Active ES2369110T3 (es) | 2006-12-19 | 2007-12-19 | Agente de revestimiento con alta resistencia al rayado y estabilidad a la intemperie. |
| ES07856913T Active ES2409182T3 (es) | 2006-12-19 | 2007-12-19 | Producto de revestimiento con alta resistencia al rayado y estabilidad a la intemperie |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US9353287B2 (enExample) |
| EP (3) | EP2091988B1 (enExample) |
| JP (3) | JP2010513617A (enExample) |
| KR (3) | KR20090094377A (enExample) |
| CN (3) | CN101583643B (enExample) |
| AT (1) | ATE515523T1 (enExample) |
| BR (3) | BRPI0721292A2 (enExample) |
| CA (3) | CA2671663A1 (enExample) |
| ES (3) | ES2408171T3 (enExample) |
| MX (3) | MX2009005536A (enExample) |
| PL (3) | PL2102263T3 (enExample) |
| RU (3) | RU2467028C2 (enExample) |
| WO (3) | WO2008074491A1 (enExample) |
Families Citing this family (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005045150A1 (de) * | 2005-09-22 | 2007-04-05 | Basf Coatings Ag | Verwendung von Phosphonsäurediestern und Diphosphonsäurediestern sowie thermisch härtbare Gemische, enthaltend Phosphonsäurediester und Diphosphonsäurediester |
| DE102005045228A1 (de) * | 2005-09-22 | 2007-04-05 | Basf Coatings Ag | Verwendung von Phosphonsäurediestern und Diphosphonsäurediestern sowie silangruppenhaltige, härtbare Gemische, enthaltend Phosphonsäurediester und Diphosphonsäurediester |
| DE102006024823A1 (de) * | 2006-05-29 | 2007-12-06 | Basf Coatings Ag | Verwendung von härtbaren Gemischen, enthaltend silangruppenhaltige Verbindungen sowie Phosphonsäurediester oder Diphosphonsäurediester, als Haftvermittler |
| CA2671663A1 (en) | 2006-12-19 | 2008-06-26 | Basf Coatings Ag | Coating compositions with high scratch resistance and weathering stability |
| DE102007014720A1 (de) * | 2007-03-23 | 2008-09-25 | Basf Coatings Japan Ltd., Yokohama | Phosphonat-haltiges Zweikomponenten-Lacksystem, dessen Herstellung und Verwendung |
| JP4829837B2 (ja) * | 2007-04-27 | 2011-12-07 | 関西ペイント株式会社 | 複層塗膜形成方法 |
| DE102007061854A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061856A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061855A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102008030304A1 (de) | 2008-06-25 | 2009-12-31 | Basf Coatings Ag | Verwendung teilsilanisierter Verbindungen auf Polyisocyanatbasis als Vernetzungsmittel in Beschichtungszusammensetzungen und Beschichtungszusammensetzung enthaltend die Verbindungen |
| DE102008043218A1 (de) | 2008-09-24 | 2010-04-01 | Evonik Goldschmidt Gmbh | Polymere Werkstoffe sowie daraus bestehende Kleber- und Beschichtungsmittel auf Basis multialkoxysilylfunktioneller Präpolymerer |
| DE102008060454A1 (de) * | 2008-12-05 | 2010-06-10 | Basf Coatings Ag | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzbeständigkeit und Witterungsstabilität sowie guten optischen Eigenschaften |
| DE102009016195A1 (de) * | 2009-04-03 | 2010-10-07 | Basf Coatings Ag | Feuchtigkeitshärtende Beschichtungsmittel auf der Basis aprotischer Lösemittel enthaltend Bindemittel mit Alkoxysilangruppen und deren Verwendung |
| DE102009022631A1 (de) | 2009-05-25 | 2010-12-16 | Evonik Goldschmidt Gmbh | Härtbare Silylgruppen enthaltende Zusammensetzungen und deren Verwendung |
| DE102009030481A1 (de) | 2009-06-24 | 2011-01-05 | Basf Coatings Gmbh | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit bei gleichzeitig guten Ergebnissen in der Prüfung der Erichsentiefung und guten Steinschlagschutzeigenschaften |
| DE102009041380A1 (de) * | 2009-09-12 | 2011-03-24 | Basf Coatings Gmbh | Bindemittelmischung und sie enthaltende Beschichtungsmittel sowie daraus hergestellte Beschichtungen mit hoher Kratzbeständigkeit und Witterungsstabilität sowie guten optischen Eigenschaften |
| DE102009054071A1 (de) * | 2009-11-20 | 2011-05-26 | Basf Coatings Gmbh | Beschichtungsmittel mit guter Lagerbeständigkeit und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit bei gleichzeitig guter Witterungsbeständigkeit |
| DE102010015683A1 (de) | 2010-04-21 | 2011-10-27 | Basf Coatings Gmbh | Beschichtungsmittel mit hohem Festkörpergehalt und gutem Verlauf sowie daraus hergestellte Mehrschichtlackierungen und deren Verwendung |
| CN102844349B (zh) * | 2010-04-21 | 2015-01-14 | 巴斯夫涂料有限公司 | 具有高固含量和良好流平性的涂层剂以及由此制备的多层涂漆及其用途 |
| DE102010015675A1 (de) * | 2010-04-21 | 2011-10-27 | Basf Coatings Gmbh | Beschichtungsmittel mit verbesserter Ablaufneigung |
| US9328257B2 (en) | 2010-11-19 | 2016-05-03 | Basf Coatings Gmbh | Coating composition having a high solids content and good levelling and also multilayer surface coatings produced therefrom and their use |
| US9029491B2 (en) * | 2010-12-22 | 2015-05-12 | Teknologisk Institut | Repellent coating composition and coating, method for making and uses thereof |
| JP6099571B2 (ja) * | 2011-01-20 | 2017-03-22 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 水性ポリウレタン被覆剤および当該被覆剤から製造された、高い耐引掻性および良好な耐化学薬品性を有する被覆 |
| EP2686361B1 (de) * | 2011-03-14 | 2014-11-26 | BASF Coatings GmbH | Polyurethan-beschichtungsmittelzusammensetzung, mehrstufige beschichtungsverfahren unter verwendung dieser beschichtungsmittelzusammensetzungen sowie die verwendung der beschichtungsmittelzusammensetzung als klarlack und pigmentierter lack bzw. anwendung des beschichtungsverfahrens für die automobilreparaturlackierung und/oder für die beschichtung von kunststoffsubstraten und/oder nutzfahrzeugen |
| AU2012228648B2 (en) * | 2011-03-14 | 2015-01-22 | Basf Coatings Gmbh | Polyurethane coating material composition, multistage coating methods using these coating material compositions, and also the use of the coating material composition as clearcoat material and pigmented coating material, and application of the coating method for automotive refinish and/or for the coating of plastics substrates and/or of utility vehicles |
| US9371469B2 (en) | 2011-06-09 | 2016-06-21 | Basf Coatings Gmbh | Coating agent compositions, coatings made therefrom and exhibiting high scratch resistance and good polishability, and use thereof |
| EP2718342B1 (de) * | 2011-06-09 | 2016-08-03 | BASF Coatings GmbH | Beschichtungsmittelzusammensetzungen und daraus hergestellte beschichtungen mit hoher kratzfestigkeit bei gleichzeitig guter polierbarkeit sowie deren verwendung |
| CN103517931B (zh) | 2011-06-09 | 2015-11-25 | 巴斯夫涂料有限公司 | 涂布剂组合物和由其制得的具有高耐划伤性且同时具有良好的可抛光性的涂层及其用途 |
| US9035082B2 (en) | 2011-10-10 | 2015-05-19 | Cytonix, Llc | Low surface energy touch screens, coatings, and methods |
| ES2684145T3 (es) | 2011-11-17 | 2018-10-01 | Basf Coatings Gmbh | Materiales de recubrimiento que contienen diésteres de glicerina y su uso en pinturas de varias capas |
| US9493661B2 (en) * | 2011-11-17 | 2016-11-15 | Basf Coatings Gmbh | Glycerol diesters, method for producing same, and use of same in coatings materials |
| US9090797B2 (en) * | 2011-12-02 | 2015-07-28 | Ppg Industries Ohio, Inc. | Method of mitigating ice build-up on a substrate |
| DE102012204290A1 (de) | 2012-03-19 | 2013-09-19 | Evonik Degussa Gmbh | Addukte aus Isocyanatoalkyl-trialkoxysilanen und aliphatischen, alkyl-verzweigten Diolen oder Polyolen |
| CN104203992B (zh) * | 2012-03-30 | 2016-08-24 | 太阳控股株式会社 | 聚(甲基)丙烯酸酯及制造方法、单体组合物、固化物和印刷电路板 |
| CN104487473B (zh) * | 2012-07-25 | 2017-05-17 | 巴斯夫涂料有限公司 | 聚氨酯涂料组合物、多阶段涂覆方法 |
| CN104487472B (zh) * | 2012-07-25 | 2017-07-14 | 巴斯夫涂料有限公司 | 聚氨酯涂料组合物及其用途、多阶段涂覆方法 |
| WO2014026780A1 (en) | 2012-08-16 | 2014-02-20 | Basf Coatings Gmbh | Coating compositions containing benzotrizol based uv-absorbers |
| MX365288B (es) * | 2012-12-03 | 2019-05-29 | Basf Coatings Gmbh | Composiciones de material de revestimiento y revestimientos producidos a partir de las mismas, que combinan alta resistencia a raspaduras con buena capacidad de pulido y buenas propiedades ópticas, y uso de las mismas. |
| JP6363615B2 (ja) | 2012-12-03 | 2018-07-25 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | エフェクト及び／または色彩付与多層塗膜塗装系ならびにそれを製造する方法、ならびにそれを使用する方法 |
| KR101392725B1 (ko) * | 2013-02-08 | 2014-05-08 | 전북대학교산학협력단 | 수용성 방염액, 목재의 방염 공정처리 방법, 이에 의한 방염목재 |
| US10579497B2 (en) * | 2013-02-26 | 2020-03-03 | Red Hat, Inc. | Providing context simulation |
| EP3083078B1 (de) | 2013-12-18 | 2019-02-27 | BASF Coatings GmbH | Verfahren zur herstellung einer mehrschichtlackierung |
| EP3083079B1 (de) | 2013-12-18 | 2020-01-08 | BASF Coatings GmbH | Verfahren zur herstellung einer mehrschichtlackierung |
| BR112016012328B1 (pt) | 2013-12-18 | 2021-11-23 | Basf Coatings Gmbh | Método para produzir um sistema de pintura de multirrevestimento e sistema de pintura de multirrevestimento |
| EP2886207A1 (de) | 2013-12-18 | 2015-06-24 | BASF Coatings GmbH | Verfahren zur Herstellung einer Mehrschichtlackierung |
| EP2896639A1 (de) | 2014-01-15 | 2015-07-22 | BASF Coatings GmbH | Beschichtete metallisierte Oberflächen |
| US9606088B2 (en) * | 2014-03-17 | 2017-03-28 | Prism Analytical Technologies, Inc. | Process and system for rapid sample analysis |
| US10144198B2 (en) | 2014-05-02 | 2018-12-04 | Corning Incorporated | Strengthened glass and compositions therefor |
| CN106715511B (zh) | 2014-09-24 | 2021-01-12 | 巴斯夫涂料有限公司 | 适合制备二道底漆涂层的涂料组合物的附着增进剂 |
| EP3227351B1 (de) | 2014-12-02 | 2019-11-06 | BASF Coatings GmbH | Copolymer und pigmentierte beschichtungsmittel enthaltend das copolymer |
| JP6619007B2 (ja) | 2014-12-02 | 2019-12-11 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 顔料入りコーティング剤および当該顔料入りコーティング剤から作製されたコーティング |
| JP6619008B2 (ja) * | 2014-12-08 | 2019-12-11 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | コーティング材料組成物、およびそれらから生成されるコーティング、ならびにその使用方法 |
| EP3230334B1 (de) * | 2014-12-08 | 2019-05-01 | BASF Coatings GmbH | Nichtwässrige beschichtungsmittelzusammensetzungen, daraus hergestellte beschichtungen mit verbesserter haftung und kratzfestigkeit sowie deren verwendung |
| RU2581975C1 (ru) * | 2014-12-10 | 2016-04-20 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Юго-Западный государственный университет" (ЮЗГУ) | Устройство автоматизированного регулирования расхода тепла на отоплениев системах теплоснабжения |
| US11479633B2 (en) * | 2015-01-22 | 2022-10-25 | Akzo Nobel Coatings International B.V. | Coating material, system based on Li/Bi catalysts |
| MX377494B (es) * | 2015-01-22 | 2025-03-10 | Basf Coatings Gmbh | Sistema de materiales de recubrimiento a base de polioles de bajo numero acido. |
| EP3271411B8 (de) | 2015-03-17 | 2024-02-14 | Covestro Deutschland AG | Silangruppen enthaltende polyisocyanate auf basis von 1,5-diisocyanatopentan |
| DK3078723T3 (en) | 2015-04-09 | 2019-02-25 | Evonik Degussa Gmbh | ADDUCTORS OF ISOCYANATOALKYL TRIMETHOXYSILANES AND WITH THEIR REACTIVE FLAMMIT PROTECTORS |
| ES2978136T3 (es) | 2015-04-21 | 2024-09-05 | Covestro Deutschland Ag | Plástico de poliisocianurato que contiene grupos siloxano y método para la producción del mismo |
| EP3292164B1 (de) | 2015-05-06 | 2021-12-08 | BASF Coatings GmbH | Verfahren zur herstellung einer mehrschichtlackierung |
| ES2727412T3 (es) | 2015-05-21 | 2019-10-16 | Covestro Deutschland Ag | Composiciones de revestimiento de poliuretano |
| CN107743510A (zh) * | 2015-06-15 | 2018-02-27 | 巴斯夫涂料有限公司 | 涂覆轮辋的方法及以此得到的防污和防制动粉尘的涂层 |
| JP6608462B2 (ja) * | 2015-06-15 | 2019-11-20 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | ポリウレタン被覆剤組成物及び多層被覆塗装系を製造するためのその使用 |
| CN107771200A (zh) * | 2015-06-15 | 2018-03-06 | 巴斯夫涂料有限公司 | 涂覆轮辋的方法及以此得到的防污和防制动粉尘的涂层 |
| KR102555281B1 (ko) | 2015-09-09 | 2023-07-14 | 코베스트로 도이칠란트 아게 | 스크래치-내성 2-성분 폴리우레탄 코팅 |
| WO2017042175A1 (en) | 2015-09-09 | 2017-03-16 | Covestro Deutschland Ag | Scratch-resistant aqueous 2k pu coatings |
| JP6756821B2 (ja) | 2015-09-30 | 2020-09-16 | エボニック オペレーションズ ゲーエムベーハー | シリコーン樹脂で変性されたイソシアナトアルキルアルコキシシラン付加物およびその使用 |
| PL3380567T3 (pl) | 2015-11-26 | 2023-01-02 | Basf Coatings Gmbh | Sposób wytwarzania wielowarstwowej powłoki lakierniczej |
| CN109153767B (zh) | 2016-05-24 | 2021-09-24 | 巴斯夫涂料有限公司 | 涂覆剂和由其制备的具有改进抗污性和清洁性的涂层及其用途 |
| US10844161B2 (en) | 2016-08-09 | 2020-11-24 | Covestro Deutschland Ag | Silane-functional polymeric polyurethanes |
| US11664491B2 (en) | 2016-09-06 | 2023-05-30 | Johnson Matthey Plc | Anode for an electrochemical cell |
| JP7333314B2 (ja) | 2017-09-29 | 2023-08-24 | ディディピー スペシャルティ エレクトロニック マテリアルズ ユーエス，エルエルシー | シラン化アクリルポリオールに基づくコーティングにプライマーレスで結合するイソシアネート官能性接着剤 |
| WO2020040738A1 (en) | 2018-08-21 | 2020-02-27 | Evonik Degussa Gmbh | Heat-curable coating compositions containing silane-functional polyurethane resins catalyzed by amidine salts |
| WO2020074297A1 (de) | 2018-10-12 | 2020-04-16 | Basf Coatings Gmbh | Verfahren zur herstellung einer mehrschichtlackierung durch post- additivierung mindestens eines basislacks mit einer wässrigen dispersion, enthaltend polyamide und/oder amidwachse |
| US12234386B2 (en) * | 2018-12-05 | 2025-02-25 | Sunstar Engineering Inc. | Urethane-based adhesive for automobile |
| ES2974421T3 (es) | 2019-01-23 | 2024-06-27 | Basf Coatings Gmbh | Agente acuoso de recubrimiento que tiene ácido policarboxílico con alineación mejorada de pigmento de efecto |
| CN113874447A (zh) | 2019-04-26 | 2021-12-31 | 巴斯夫涂料有限公司 | 水性涂料组合物及使用所述组合物形成多层涂膜的方法 |
| US20220213346A1 (en) * | 2019-05-06 | 2022-07-07 | Basf Coatings Gmbh | Silane-based coating composition |
| EP3760658A1 (de) | 2019-07-03 | 2021-01-06 | Covestro Deutschland AG | Beständige 2k-pur-beschichtungen |
| MX2022001224A (es) | 2019-07-29 | 2022-03-02 | Basf Coatings Gmbh | Proceso para producir un recubrimiento multicapa que comprende una capa de recubrimiento brillante y un recubrimiento multicapa obtenido de dicho proceso. |
| JP2022553977A (ja) | 2019-10-23 | 2022-12-27 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | ピンホールに対する安定性が改善された顔料入り水性コーティング組成物 |
| JP7462765B2 (ja) | 2020-01-21 | 2024-04-05 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | 改善されたレベリング特性を有する水性ポリカルボン酸含有コーティング組成物 |
| US20230211530A1 (en) | 2020-07-02 | 2023-07-06 | Covestro Deutschland Ag | Coatings from polyisocyanurate coatings (rim) and their use in injection molding processes |
| WO2022167173A1 (en) | 2021-02-03 | 2022-08-11 | Basf Coatings Gmbh | Method for forming a multilayer coating and object coated with such a multilayer coating |
| MX2023012664A (es) | 2021-04-28 | 2023-11-07 | Basf Coatings Gmbh | Compuestos de tioeter hidroxilo-funcionales y su uso en composiciones curables. |
| EP4108695A1 (de) | 2021-06-21 | 2022-12-28 | Covestro Deutschland AG | Beschichtungsmittel und daraus erhältliche beschichtungen mit verbesserten anschmutzungsresistenzen und (selbst-)reinigungseigenschaften |
| EP4108694A1 (de) | 2021-06-21 | 2022-12-28 | Covestro Deutschland AG | Beschichtungsmittel und daraus erhältliche beschichtungen mit verbesserten anschmutzungsresistenzen und (selbst-)reinigungseigenschaften |
| EP4108697A1 (de) | 2021-06-21 | 2022-12-28 | Covestro Deutschland AG | Beschichtungsmittel und daraus erhältliche beschichtungen mit verbesserten anschmutzungsresistenzen und (selbst-)reinigungseigenschaften |
| EP4186951B1 (de) | 2021-11-30 | 2025-01-08 | BASF Coatings GmbH | Verfahren zur herstellung einer mehrschichtlackierung |
| EP4198094A1 (de) | 2021-12-20 | 2023-06-21 | Covestro Deutschland AG | Mehrschichtaufbau auf metallischen untergründen basierend auf polyaspartatbeschichtungen |
| WO2023117883A1 (en) | 2021-12-21 | 2023-06-29 | Basf Se | Chemical product passport |
| EP4584343A1 (en) | 2022-09-05 | 2025-07-16 | BASF Coatings GmbH | Aqueous coating material containing cellulose nanofibers |
| CN115433508B (zh) * | 2022-09-16 | 2023-04-18 | 天津森聚柯密封涂层材料有限公司 | 一种单组分高强度弹性涂料及其制备方法和应用 |
| EP4357420A1 (en) | 2022-10-17 | 2024-04-24 | BASF Coatings GmbH | Process for sustainably coating automotive substrates |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3168483A (en) * | 1961-01-17 | 1965-02-02 | Air Prod & Chem | Diazabicyclooctane-alkylene oxide catalyst compositions |
| US3707521A (en) * | 1970-03-05 | 1972-12-26 | Essex Chemical Corp | Polyurethane sealant-primer system isocyanate-reactive surface primer composition for polyurethane sealants |
| US3718614A (en) | 1971-02-23 | 1973-02-27 | American Cyanamid Co | Polymeric viscosity control additives for silica thixotropic compositions |
| US3959403A (en) * | 1975-03-31 | 1976-05-25 | General Electric Company | Process for making silarylenesilanediol, silarylenesiloxanediol and silarylenesiloxane-polydiorganosiloxane block copolymers |
| DE2835451C2 (de) | 1978-08-12 | 1985-10-24 | Saarbergwerke AG, 6600 Saarbrücken | Verfahren zum Verfestigen von Kohle und/oder Gestein im Bergbau |
| JPS5536216A (en) * | 1978-09-05 | 1980-03-13 | Mitsubishi Gas Chem Co Inc | Curing of organoalkoxysilane compound |
| US4479990A (en) | 1982-07-30 | 1984-10-30 | Westinghouse Electric Co. | Arc and track resistant articles utilizing photosensitive sag resistant cycloaliphatic epoxy resin coating compositions |
| JPS59124954A (ja) * | 1982-12-30 | 1984-07-19 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物 |
| US4499151A (en) * | 1983-03-29 | 1985-02-12 | Ppg Industries, Inc. | Color plus clear coating method utilizing addition interpolymers containing alkoxy silane and/or acyloxy silane groups |
| US4499150A (en) | 1983-03-29 | 1985-02-12 | Ppg Industries, Inc. | Color plus clear coating method utilizing addition interpolymers containing alkoxy silane and/or acyloxy silane groups |
| US4508887A (en) * | 1983-08-01 | 1985-04-02 | Dow Corning Corporation | Method and novel catalyst compositions for preparing polyorganosiloxanes |
| US4598131A (en) * | 1984-12-19 | 1986-07-01 | Ppg Industries, Inc. | Catalysts for curable coating vehicle based upon aminoalkyloxy silanes and organic isocyanates |
| US4710542A (en) | 1986-05-16 | 1987-12-01 | American Cyanamid Company | Alkylcarbamylmethylated amino-triazine crosslinking agents and curable compositions containing the same |
| EP0249201A3 (en) | 1986-06-10 | 1989-07-19 | Union Carbide Corporation | High solids sag resistant cycloaliphatic epoxy coatings containing low molecular weight high tg organic polymeric sag resisting additives |
| NO170944C (no) * | 1987-01-24 | 1992-12-30 | Akzo Nv | Fortykkede, vandige preparater, samt anvendelse av slike |
| SU1654318A1 (ru) * | 1987-09-30 | 1991-06-07 | Московский Инженерно-Строительный Институт Им.В.В.Куйбышева | Способ приготовлени композиций дл нанесени покрытий спортивных площадок |
| JP2719420B2 (ja) * | 1989-10-19 | 1998-02-25 | 鐘淵化学工業株式会社 | 加水分解性シリル基含有ビニル系重合体の製造方法 |
| US5250605A (en) * | 1990-12-17 | 1993-10-05 | E. I. Du Pont De Nemours And Company | Coating compositions comprising an organosilane polymer and reactive dispersed polymers |
| US5225248A (en) * | 1991-05-13 | 1993-07-06 | E. I. Du Pont De Nemours And Company | Method of curing a topcoat |
| DE4132430A1 (de) | 1991-09-28 | 1993-04-01 | Basf Lacke & Farben | Waessrige lacke und verfahren zur herstellung von automobildecklackierungen |
| JP3086737B2 (ja) | 1992-01-17 | 2000-09-11 | 鐘淵化学工業株式会社 | 塗料用硬化性組成物 |
| EP0554684B1 (en) | 1992-01-17 | 1996-01-03 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition for paint |
| DE4204518A1 (de) * | 1992-02-15 | 1993-08-19 | Basf Lacke & Farben | Verfahren zur herstellung einer zweischichtigen lackierung und fuer dieses verfahren geeignete nicht-waessrige lacke |
| JP3144872B2 (ja) | 1992-02-27 | 2001-03-12 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| GB9210653D0 (en) | 1992-05-19 | 1992-07-01 | Ici Plc | Silane functional oligomer |
| US5238993A (en) * | 1992-10-02 | 1993-08-24 | The Dow Chemical Company | Primer composition for improving the bonding of urethane adhesives to acid resistant paints |
| DE4310413A1 (de) | 1993-03-31 | 1994-10-06 | Basf Lacke & Farben | Nichtwäßriger Lack und Verfahren zur Herstellung einer zweischichtigen Decklackierung |
| DE4310414A1 (de) | 1993-03-31 | 1994-10-06 | Basf Lacke & Farben | Verfahren zur Herstellung einer zweischichtigen Decklackierung auf einer Substratoberfläche |
| JP3482569B2 (ja) | 1994-06-14 | 2003-12-22 | 鐘淵化学工業株式会社 | 塗料用樹脂組成物、及び耐汚染性に優れた塗膜の形成方法 |
| NZ303624A (en) * | 1995-03-08 | 1999-01-28 | Du Pont | Reactive organosilicons as coatings, adhesives, and sealants |
| WO1997012945A1 (en) | 1995-10-06 | 1997-04-10 | Cabot Corporation | Aqueous thixotropes for waterborne systems |
| DE19624972C2 (de) * | 1996-06-22 | 1998-06-04 | Herberts Gmbh | Wäßrige Dispersion von silanfunktionellen Polyurethanharzen, deren Herstellung und Verwendung |
| US5747590A (en) * | 1996-12-04 | 1998-05-05 | E. I. Du Pont De Nemours And Company | Acrylic-melamine-functionalized oligomer coating composition |
| US5691439A (en) * | 1996-12-16 | 1997-11-25 | Bayer Corporation | Low surface energy polyisocyanates and their use in one- or two-component coating compositions |
| JPH10306251A (ja) | 1997-05-07 | 1998-11-17 | Kanegafuchi Chem Ind Co Ltd | 塗料用硬化性組成物およびそれを塗布してなる塗装物 |
| SE510128C2 (sv) | 1997-06-26 | 1999-04-19 | Perstorp Ab | Förfarande för framställning av dendritisk polyol |
| JPH11116847A (ja) | 1997-10-09 | 1999-04-27 | Kanegafuchi Chem Ind Co Ltd | 上塗り塗料組成物およびその塗膜の形成方法 |
| US5952445A (en) | 1998-04-09 | 1999-09-14 | Bayer Corporation | Water dispersible compounds containing alkoxysilane groups |
| US5985463A (en) * | 1998-06-24 | 1999-11-16 | E.I. Du Pont De Nemours And Company | Coating containing hydroxy containing acrylosilane polymer to improve mar and acid etch resistance |
| US6046270A (en) | 1998-10-14 | 2000-04-04 | Bayer Corporation | Silane-modified polyurethane resins, a process for their preparation and their use as moisture-curable resins |
| DE19855619A1 (de) * | 1998-12-02 | 2000-06-08 | Wacker Chemie Gmbh | Unter Abspaltung von Alkoholen zu Elastomeren vernetzbare Organopolysiloxanmassen |
| BR0010514A (pt) * | 1999-03-17 | 2002-01-08 | Du Pont | Composição de revestimento transparente de elevado teor de sólidos resistente à corrosão ácida e método de produção de um revestimento transparente em um substrato |
| DE60033403T2 (de) | 1999-07-30 | 2007-10-31 | Ppg Industries Ohio, Inc. | Beschichtungszusammensetzungen mit verbesserter kratzfestigkeit, beschichtete oberfläche und verfahren zu deren herstellung |
| US6239211B1 (en) * | 2000-01-24 | 2001-05-29 | Dow Corning Corporation | Emulsions containing silicone polymers |
| KR20020081408A (ko) * | 2000-03-13 | 2002-10-26 | 아크조 노벨 엔.브이. | 이소시아네이트-관능기 화합물, 이소시아네이트-반응성화합물 및 공촉매를 포함하는 조성물 |
| WO2001098393A1 (en) | 2000-06-22 | 2001-12-27 | Basf Corporation | Coating compositions having improved adhesion to aluminum substrates |
| DE10048615A1 (de) | 2000-09-30 | 2002-04-11 | Degussa | Nichtwäßriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| EP1197506B1 (en) | 2000-10-13 | 2006-01-25 | Tosoh Corporation | Catalyst for production of a two component polyurethane sealant |
| US6379807B1 (en) * | 2000-11-07 | 2002-04-30 | E. I. Du Pont De Nemours And Company | Coating composition having improved acid etch resistance |
| DE10103027A1 (de) | 2001-01-24 | 2002-07-25 | Bayer Ag | Zweikomponenten-Polyurethan-Bindemittel als Haftvermittler |
| DE10132938A1 (de) * | 2001-07-06 | 2003-01-16 | Degussa | Nichtwässriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| US6642309B2 (en) * | 2001-08-14 | 2003-11-04 | Kaneka Corporation | Curable resin composition |
| AT412090B (de) | 2002-01-29 | 2004-09-27 | Surface Specialties Austria | Hydroxyfunktionelle polyester |
| DE10219508A1 (de) | 2002-04-30 | 2003-11-13 | Basf Ag | Verfahren zur Herstellung hochfunktioneller, hyperverzweigter Polyester |
| US7056976B2 (en) * | 2002-08-06 | 2006-06-06 | Huntsman International Llc | Pultrusion systems and process |
| US20040077778A1 (en) | 2002-08-07 | 2004-04-22 | Isidor Hazan | One-pack primer sealer compositions for SMC automotive body panels |
| DE10352907A1 (de) | 2002-11-15 | 2004-08-05 | Henkel Kgaa | Silylgruppen enthaltende Präpolymere, deren Herstellung und Verwendung in Montageschäumen |
| JP4360811B2 (ja) * | 2003-02-04 | 2009-11-11 | 新日本製鐵株式会社 | プレス成形性と加工部耐食性に優れたプレコート金属板 |
| DE10323206A1 (de) * | 2003-05-22 | 2004-12-09 | Consortium für elektrochemische Industrie GmbH | Schäumbare Mischungen |
| EP1496114A1 (de) | 2003-07-07 | 2005-01-12 | Margraf, Stefan, Dr.med. | Verfahren zur Inaktivierung von Mikroorganismen |
| EP1502927A1 (de) | 2003-07-31 | 2005-02-02 | Sika Technology AG | Isocyanatfreie Primerzusammensetzung für Glas und Glaskeramiken |
| DE10344448A1 (de) * | 2003-09-25 | 2005-04-28 | Henkel Kgaa | Bindemittel mit Barriere-Eigenschaft |
| US20050208312A1 (en) | 2004-03-17 | 2005-09-22 | Isidor Hazan | One-pack primer surfacer composition for SMC automotive body panels |
| US20050238899A1 (en) * | 2004-04-27 | 2005-10-27 | Isao Nagata | High solids clearcoat compositions containing silane functional compounds |
| DE102004026904A1 (de) | 2004-06-01 | 2005-12-22 | Basf Ag | Hochfunktionelle, hoch- oder hyperverzweigte Polyester sowie deren Herstellung und Verwendung |
| US7871669B2 (en) | 2004-08-30 | 2011-01-18 | E.I. Du Pont De Nemours And Company | Method for achieving a durable two-tone finish on a vehicle |
| DE102004050748A1 (de) | 2004-10-19 | 2006-04-20 | Basf Coatings Aktiengesellschaft | Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilanen |
| DE102004050747A1 (de) | 2004-10-19 | 2006-04-27 | Basf Coatings Ag | Beschichtungsmittel enthaltend Addukte mit Alkoxysilanfunktionalität |
| DE102004050746A1 (de) * | 2004-10-19 | 2006-04-20 | Basf Coatings Ag | Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilan-funktionellen Komponenten |
| DE102005003299A1 (de) | 2005-01-24 | 2006-07-27 | Goldschmidt Gmbh | Nanopartikel für die Herstellung von Polyurethanschaum |
| ES2316066T3 (es) | 2005-03-11 | 2009-04-01 | The Sherwin-Williams Company | Composicion de revestimiento curable resistente al rayado. |
| FR2886284B1 (fr) | 2005-05-30 | 2007-06-29 | Commissariat Energie Atomique | Procede de realisation de nanostructures |
| DE102005026085A1 (de) | 2005-06-07 | 2006-12-14 | Construction Research & Technology Gmbh | Silan-modifizierte Harnstoff-Derivate, Verfahren zu ihrer Herstellung und deren Verwendung als Rheologiehilfsmittel |
| FR2887996B1 (fr) | 2005-06-30 | 2007-08-17 | Prismaflex Internat Sa | Panneau de communication retroeclaire |
| WO2007016234A2 (en) | 2005-07-29 | 2007-02-08 | E. I. Du Pont De Nemours And Company | Method for producing damage resistant multi-layer coatings on an automotive body or part thereof |
| US7858190B2 (en) | 2005-09-15 | 2010-12-28 | Basf Coatings Gmbh | Thermosetting coating compositions with multiple cure mechanisms |
| DE102005045228A1 (de) * | 2005-09-22 | 2007-04-05 | Basf Coatings Ag | Verwendung von Phosphonsäurediestern und Diphosphonsäurediestern sowie silangruppenhaltige, härtbare Gemische, enthaltend Phosphonsäurediester und Diphosphonsäurediester |
| DE102006024823A1 (de) | 2006-05-29 | 2007-12-06 | Basf Coatings Ag | Verwendung von härtbaren Gemischen, enthaltend silangruppenhaltige Verbindungen sowie Phosphonsäurediester oder Diphosphonsäurediester, als Haftvermittler |
| US20080075871A1 (en) | 2006-09-21 | 2008-03-27 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| CA2671663A1 (en) | 2006-12-19 | 2008-06-26 | Basf Coatings Ag | Coating compositions with high scratch resistance and weathering stability |
| DE102007013242A1 (de) | 2007-03-15 | 2008-09-18 | Basf Coatings Ag | Hochkratzfeste Beschichtung mit guter Witterungs- und Rissbeständigkeit |
| DE102007026722A1 (de) | 2007-06-06 | 2008-12-11 | Basf Coatings Japan Ltd., Yokohama | Klarlackzusammensetzungen enthaltend hyperverzweigte, dendritische hydroxyfunktionelle Polyester |
| DE102007061856A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061855A1 (de) | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061854A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102008030304A1 (de) * | 2008-06-25 | 2009-12-31 | Basf Coatings Ag | Verwendung teilsilanisierter Verbindungen auf Polyisocyanatbasis als Vernetzungsmittel in Beschichtungszusammensetzungen und Beschichtungszusammensetzung enthaltend die Verbindungen |
| DE102008060454A1 (de) | 2008-12-05 | 2010-06-10 | Basf Coatings Ag | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzbeständigkeit und Witterungsstabilität sowie guten optischen Eigenschaften |
| DE102009024103A1 (de) * | 2009-06-06 | 2010-12-09 | Basf Coatings Gmbh | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit und hoher Kocherstabilität |
| DE102009030481A1 (de) | 2009-06-24 | 2011-01-05 | Basf Coatings Gmbh | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit bei gleichzeitig guten Ergebnissen in der Prüfung der Erichsentiefung und guten Steinschlagschutzeigenschaften |
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2007
- 2007-12-19 CA CA002671663A patent/CA2671663A1/en not_active Abandoned
- 2007-12-19 JP JP2009541878A patent/JP2010513617A/ja active Pending
- 2007-12-19 MX MX2009005536A patent/MX2009005536A/es active IP Right Grant
- 2007-12-19 BR BRPI0721292-5A2A patent/BRPI0721292A2/pt not_active IP Right Cessation
- 2007-12-19 RU RU2009127640/04A patent/RU2467028C2/ru not_active IP Right Cessation
- 2007-12-19 US US12/519,449 patent/US9353287B2/en active Active
- 2007-12-19 CN CN2007800466688A patent/CN101583643B/zh not_active Expired - Fee Related
- 2007-12-19 CA CA2671516A patent/CA2671516C/en active Active
- 2007-12-19 ES ES07856914T patent/ES2408171T3/es active Active
- 2007-12-19 BR BRPI0721070-1A2A patent/BRPI0721070A2/pt not_active IP Right Cessation
- 2007-12-19 WO PCT/EP2007/011192 patent/WO2008074491A1/de not_active Ceased
- 2007-12-19 KR KR1020097015003A patent/KR20090094377A/ko not_active Ceased
- 2007-12-19 JP JP2009541879A patent/JP5631004B2/ja active Active
- 2007-12-19 ES ES07856915T patent/ES2369110T3/es active Active
- 2007-12-19 MX MX2009005613A patent/MX2009005613A/es active IP Right Grant
- 2007-12-19 EP EP07856914A patent/EP2091988B1/de not_active Revoked
- 2007-12-19 JP JP2009541877A patent/JP5637687B2/ja active Active
- 2007-12-19 PL PL07856915T patent/PL2102263T3/pl unknown
- 2007-12-19 WO PCT/EP2007/011191 patent/WO2008074490A1/de not_active Ceased
- 2007-12-19 KR KR1020097015002A patent/KR101500460B1/ko active Active
- 2007-12-19 US US12/519,458 patent/US8569438B2/en active Active
- 2007-12-19 RU RU2009127635/04A patent/RU2467026C2/ru active
- 2007-12-19 RU RU2009127638/04A patent/RU2467027C2/ru active
- 2007-12-19 PL PL07856914T patent/PL2091988T3/pl unknown
- 2007-12-19 US US12/519,466 patent/US20100015344A1/en not_active Abandoned
- 2007-12-19 ES ES07856913T patent/ES2409182T3/es active Active
- 2007-12-19 CN CN2007800467267A patent/CN101563382B/zh active Active
- 2007-12-19 MX MX2009005495A patent/MX2009005495A/es active IP Right Grant
- 2007-12-19 BR BRPI0721288-7A2A patent/BRPI0721288A2/pt not_active Application Discontinuation
- 2007-12-19 KR KR1020097015004A patent/KR101500462B1/ko active Active
- 2007-12-19 EP EP07856915A patent/EP2102263B1/de not_active Revoked
- 2007-12-19 PL PL07856913T patent/PL2091987T3/pl unknown
- 2007-12-19 EP EP07856913A patent/EP2091987B1/de not_active Revoked
- 2007-12-19 CA CA2671662A patent/CA2671662C/en active Active
- 2007-12-19 AT AT07856915T patent/ATE515523T1/de active
- 2007-12-19 WO PCT/EP2007/011190 patent/WO2008074489A1/de not_active Ceased
- 2007-12-19 CN CN2007800466781A patent/CN101568565B/zh active Active
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2013
- 2013-09-25 US US14/036,367 patent/US20140023789A1/en not_active Abandoned
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