DE102008015104A1 - Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate - Google Patents
Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate Download PDFInfo
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- DE102008015104A1 DE102008015104A1 DE102008015104A DE102008015104A DE102008015104A1 DE 102008015104 A1 DE102008015104 A1 DE 102008015104A1 DE 102008015104 A DE102008015104 A DE 102008015104A DE 102008015104 A DE102008015104 A DE 102008015104A DE 102008015104 A1 DE102008015104 A1 DE 102008015104A1
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- Prior art keywords
- unsubstituted
- butyl
- coating composition
- composition according
- group
- Prior art date
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- 239000008199 coating composition Substances 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims abstract description 10
- 230000008569 process Effects 0.000 title claims abstract description 9
- 239000000758 substrate Substances 0.000 title claims description 20
- 238000002360 preparation method Methods 0.000 title claims description 7
- -1 isocyanate compound Chemical class 0.000 claims abstract description 94
- 150000001875 compounds Chemical class 0.000 claims abstract description 45
- 239000000049 pigment Substances 0.000 claims abstract description 38
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 27
- 239000000945 filler Substances 0.000 claims abstract description 21
- 239000002904 solvent Substances 0.000 claims abstract description 21
- 150000004658 ketimines Chemical class 0.000 claims abstract description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000126 substance Substances 0.000 claims abstract description 15
- 150000004705 aldimines Chemical class 0.000 claims abstract description 12
- 238000000576 coating method Methods 0.000 claims abstract description 11
- 239000012948 isocyanate Substances 0.000 claims abstract description 11
- 239000011248 coating agent Substances 0.000 claims abstract description 9
- 125000001424 substituent group Chemical group 0.000 claims description 44
- 229910052731 fluorine Inorganic materials 0.000 claims description 31
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 27
- 125000002947 alkylene group Chemical group 0.000 claims description 22
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 22
- 229920005862 polyol Polymers 0.000 claims description 22
- 150000003077 polyols Chemical class 0.000 claims description 22
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 21
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 21
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 21
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 20
- 125000000732 arylene group Chemical group 0.000 claims description 18
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 17
- 239000005056 polyisocyanate Substances 0.000 claims description 17
- 229920001228 polyisocyanate Polymers 0.000 claims description 17
- 229910052782 aluminium Inorganic materials 0.000 claims description 15
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 15
- 125000004450 alkenylene group Chemical group 0.000 claims description 14
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 14
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 14
- 229910000077 silane Inorganic materials 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000004474 heteroalkylene group Chemical group 0.000 claims description 12
- 229910000831 Steel Inorganic materials 0.000 claims description 11
- 238000004040 coloring Methods 0.000 claims description 11
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 11
- 239000010959 steel Substances 0.000 claims description 11
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 claims description 10
- 235000019700 dicalcium phosphate Nutrition 0.000 claims description 10
- 150000002513 isocyanates Chemical class 0.000 claims description 10
- 150000003254 radicals Chemical class 0.000 claims description 9
- 239000012855 volatile organic compound Substances 0.000 claims description 9
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 7
- 230000008439 repair process Effects 0.000 claims description 6
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 5
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 3
- 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 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 238000006471 dimerization reaction Methods 0.000 claims description 2
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 238000006384 oligomerization reaction Methods 0.000 claims description 2
- 238000005829 trimerization reaction Methods 0.000 claims description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 239000004922 lacquer Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 abstract description 10
- 229910052742 iron Inorganic materials 0.000 abstract description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 3
- 238000009996 mechanical pre-treatment Methods 0.000 abstract description 3
- 238000005488 sandblasting Methods 0.000 abstract description 3
- 229910052725 zinc Inorganic materials 0.000 abstract description 3
- 239000011701 zinc Substances 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 23
- 238000012360 testing method Methods 0.000 description 19
- 125000005842 heteroatom Chemical group 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 12
- 239000001301 oxygen Substances 0.000 description 12
- 229910052717 sulfur Inorganic materials 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 9
- 238000005260 corrosion Methods 0.000 description 9
- 239000003973 paint Substances 0.000 description 9
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000011593 sulfur Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 150000008064 anhydrides Chemical class 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- 150000004756 silanes Chemical class 0.000 description 5
- 239000003981 vehicle Substances 0.000 description 5
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- 125000002015 acyclic group Chemical group 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 150000005840 aryl radicals Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
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- 238000005516 engineering process Methods 0.000 description 4
- 230000008595 infiltration Effects 0.000 description 4
- 238000001764 infiltration Methods 0.000 description 4
- 150000002596 lactones Chemical class 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 230000008929 regeneration Effects 0.000 description 4
- 238000011069 regeneration method Methods 0.000 description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 125000004434 sulfur atom Chemical group 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
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- 125000002950 monocyclic group Chemical group 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
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- 150000003839 salts Chemical class 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
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- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
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- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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- 239000006096 absorbing agent Substances 0.000 description 2
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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
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- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
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- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 2
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- 125000003566 oxetanyl group Chemical group 0.000 description 2
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
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- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 2
- 125000003507 tetrahydrothiofenyl group Chemical group 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
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- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- BUHVIAUBTBOHAG-FOYDDCNASA-N (2r,3r,4s,5r)-2-[6-[[2-(3,5-dimethoxyphenyl)-2-(2-methylphenyl)ethyl]amino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound COC1=CC(OC)=CC(C(CNC=2C=3N=CN(C=3N=CN=2)[C@H]2[C@@H]([C@H](O)[C@@H](CO)O2)O)C=2C(=CC=CC=2)C)=C1 BUHVIAUBTBOHAG-FOYDDCNASA-N 0.000 description 1
- GGAUUQHSCNMCAU-ZXZARUISSA-N (2s,3r)-butane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C[C@H](C(O)=O)[C@H](C(O)=O)CC(O)=O GGAUUQHSCNMCAU-ZXZARUISSA-N 0.000 description 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3253—Polyamines being in latent form
- C08G18/3256—Reaction products of polyamines with aldehydes or ketones
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- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4244—Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether 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
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
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- 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
- C08G2150/00—Compositions for coatings
- C08G2150/90—Compositions for anticorrosive coatings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Epoxy Resins (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
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|---|---|---|---|
| DE102008015104A DE102008015104A1 (de) | 2008-03-19 | 2008-03-19 | Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate |
| PL09722893T PL2271689T3 (pl) | 2008-03-19 | 2009-03-17 | Kompozycja powłokowa, sposób jej wytwarzania, jej zastosowanie i powlekane nią podłoża |
| EP09722893A EP2271689B1 (de) | 2008-03-19 | 2009-03-17 | Beschichtungszusammensetzung, verfahren zu ihrer herstellung, ihre verwendung und mit ihr beschichtete substrate |
| AU2009226736A AU2009226736B2 (en) | 2008-03-19 | 2009-03-17 | Coating composition, method for the production thereof, use thereof and substrates coated therewith |
| MX2010009958A MX2010009958A (es) | 2008-03-19 | 2009-03-17 | Composicion de revestimiento, metodo para la produccion de la misma uso de la misma y substratos revestidos con la misma. |
| US12/933,287 US9266993B2 (en) | 2008-03-19 | 2009-03-17 | Coating composition, method for the production thereof, use thereof, and substrates coated therewith |
| AT09722893T ATE533801T1 (de) | 2008-03-19 | 2009-03-17 | Beschichtungszusammensetzung, verfahren zu ihrer herstellung, ihre verwendung und mit ihr beschichtete substrate |
| ES09722893T ES2377806T3 (es) | 2008-03-19 | 2009-03-17 | Composición de revestimiento, procedimiento para su producción, utilización y sustratos revestidos con la misma |
| JP2011500107A JP5695557B2 (ja) | 2008-03-19 | 2009-03-17 | 塗料組成物、その製造方法、利用、及びそれを塗布した基板 |
| BRPI0909670A BRPI0909670A2 (pt) | 2008-03-19 | 2009-03-17 | composição de revestimento, processo para a sua produção, seu uso e substratos revestidos com esta |
| PCT/EP2009/001956 WO2009115294A1 (de) | 2008-03-19 | 2009-03-17 | Beschichtungszusammensetzung, verfahren zu ihrer herstellung, ihre verwendung und mit ihr beschichtete substrate |
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| DE102008015104A DE102008015104A1 (de) | 2008-03-19 | 2008-03-19 | Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate |
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| DE102008015104A1 true DE102008015104A1 (de) | 2009-09-24 |
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| US (1) | US9266993B2 (https=) |
| EP (1) | EP2271689B1 (https=) |
| JP (1) | JP5695557B2 (https=) |
| AT (1) | ATE533801T1 (https=) |
| AU (1) | AU2009226736B2 (https=) |
| BR (1) | BRPI0909670A2 (https=) |
| DE (1) | DE102008015104A1 (https=) |
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| MX (1) | MX2010009958A (https=) |
| PL (1) | PL2271689T3 (https=) |
| WO (1) | WO2009115294A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116496646A (zh) * | 2022-01-18 | 2023-07-28 | 苏州大学 | 一种超疏水光热涂层、其制备方法和应用 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009052934A1 (de) * | 2009-11-12 | 2011-05-19 | Lanxess Deutschland Gmbh | Borselektive Harze |
| MX2012010550A (es) * | 2010-04-21 | 2012-11-16 | Basf Coatings Gmbh | Materiales de recubrimiento con alto contenido de solidos y sistemas de pintura de multiple capa con buena nivelacion producidos de los mismos y usos de los mismos. |
| JP5943932B2 (ja) * | 2010-11-19 | 2016-07-05 | 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ＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 高固形分及び良好な流展性を有するコーティング剤並びにそれより製造された多層塗膜並びにその使用 |
| IN2014DN09667A (https=) * | 2012-06-06 | 2015-07-31 | Grace W R & Co | |
| US10980236B2 (en) | 2014-11-04 | 2021-04-20 | Allied Bioscience, Inc. | Broad spectrum antimicrobial coatings comprising combinations of organosilanes |
| US10993441B2 (en) | 2014-11-04 | 2021-05-04 | Allied Bioscience, Inc. | Antimicrobial coatings comprising organosilane homopolymers |
| CN104361836B (zh) * | 2014-11-20 | 2017-01-11 | 无锡科思电子科技有限公司 | 一种led显示屏铸铁箱体的酸洗磷化方法 |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0008127A1 (de) | 1978-08-12 | 1980-02-20 | Saarbergwerke Aktiengesellschaft | Verfahren zum Verfestigen von Kohle und/oder Gestein im Bergbau |
| EP0249201A2 (en) | 1986-06-10 | 1987-12-16 | Union Carbide Corporation | High solids sag resistant cycloaliphatic epoxy coatings containing low molecular weight high Tg organic polymeric sag resisting additives |
| EP0276501A2 (en) | 1987-01-24 | 1988-08-03 | Akzo Nobel N.V. | Thickening compositions and thickened aqueous acid solutions |
| US5214086A (en) | 1991-09-04 | 1993-05-25 | Basf Corporation | Coating compositions which may be ambient cured |
| WO1994022968A1 (de) | 1993-03-31 | 1994-10-13 | Basf Lacke + Farben Ag | Nichtwässriger thixotropierter lack und verfahren zur herstellung mehrschichtiger überzüge damit |
| EP0686654A1 (en) | 1994-06-06 | 1995-12-13 | Basf Corporation | Coating compositions comprising aldimine and siocyanate and process for their preparation |
| WO1997000693A1 (en) | 1995-06-20 | 1997-01-09 | Peptide Technology Limited | Novel formulation for peptide release |
| WO1997012945A1 (en) | 1995-10-06 | 1997-04-10 | Cabot Corporation | Aqueous thixotropes for waterborne systems |
| DE69702047T2 (de) * | 1996-02-17 | 2000-10-26 | Imperial Chemical Industries Plc, London | Beschichtungszusammensetzung |
| DE102005036630B3 (de) * | 2005-08-04 | 2006-09-14 | Basf Coatings Ag | Chromfreie, zinkarme, korrosionshemmende Pigmentmischung, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE102006044035A1 (de) * | 2006-09-14 | 2008-03-27 | Basf Coatings Ag | Calciumhydrogenphosphathaltige Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2840820A1 (de) * | 1978-09-20 | 1980-04-03 | Hoechst Ag | Verfahren zur herstellung phosphorhaltiger korrosionsschutzpigmente |
| DE2940695A1 (de) * | 1979-10-08 | 1981-04-16 | Hoechst Ag, 6000 Frankfurt | Korrosionsinhibierendes pigment |
| DE3720779A1 (de) | 1987-06-24 | 1989-01-05 | Herberts Gmbh | Beschichtungszusammensetzung fuer aluminium-legierungen und deren verwendung |
| DE4021086A1 (de) | 1990-07-03 | 1992-01-09 | Heubach Hans Dr Gmbh Co Kg | Korrosionsschutzpigmente auf der basis von tertiaeren erdalkali-aluminium-phosphaten und verfahren zu ihrer herstellung |
| US5578347A (en) * | 1994-05-24 | 1996-11-26 | E. I. Du Pont De Nemours And Company | Process for applying a finish to a metal substrate |
| NO312911B1 (no) * | 1994-12-22 | 2002-07-15 | Budenheim Rud A Oetker Chemie | Antikorrosjonspigment og anvendelse av dette |
| US6359059B1 (en) * | 1995-02-02 | 2002-03-19 | Basf Corporation | Paint compositions containing reactive urea/urethanes |
| EP0828798B1 (en) * | 1995-05-26 | 2001-08-22 | AD Aerospace Finishes v.o.f. | Coating composition having improved adhesion to substrate |
| DE19731540A1 (de) * | 1997-07-23 | 1999-01-28 | Herberts Gmbh | Überzugsmittel und deren Verwendung bei Verfahren zur Mehrschichtlackierung |
| AU1476200A (en) * | 1998-11-20 | 2000-06-13 | Sherwin-Williams Company, The | Curable compositions comprising acetoacetoxy and imine functionality |
| EP1329469A1 (de) * | 2002-01-18 | 2003-07-23 | Sika Schweiz AG | Polyurethanzusammensetzung |
| US20040096569A1 (en) * | 2002-11-15 | 2004-05-20 | Barkalow David G. | Edible film products and methods of making same |
| US7297748B2 (en) * | 2004-08-31 | 2007-11-20 | Rhodia Inc. | Direct to metal polyurethane coating compositions |
| WO2006038651A1 (ja) * | 2004-10-06 | 2006-04-13 | Kansai Paint Co., Ltd. | 活性エネルギー線硬化性塗料組成物及び塗膜形成方法 |
| CA2491308A1 (en) * | 2004-12-29 | 2006-06-30 | The Sherwin-Williams Company | Method of applying automotive primer-surfacer using a squeegee |
| US20070129527A1 (en) * | 2005-12-06 | 2007-06-07 | Griswold Roy M | Silylated polyurethane-polyurea protective coating compositions |
-
2008
- 2008-03-19 DE DE102008015104A patent/DE102008015104A1/de not_active Withdrawn
-
2009
- 2009-03-17 ES ES09722893T patent/ES2377806T3/es active Active
- 2009-03-17 EP EP09722893A patent/EP2271689B1/de active Active
- 2009-03-17 US US12/933,287 patent/US9266993B2/en not_active Expired - Fee Related
- 2009-03-17 PL PL09722893T patent/PL2271689T3/pl unknown
- 2009-03-17 BR BRPI0909670A patent/BRPI0909670A2/pt not_active IP Right Cessation
- 2009-03-17 AT AT09722893T patent/ATE533801T1/de active
- 2009-03-17 MX MX2010009958A patent/MX2010009958A/es active IP Right Grant
- 2009-03-17 AU AU2009226736A patent/AU2009226736B2/en not_active Ceased
- 2009-03-17 WO PCT/EP2009/001956 patent/WO2009115294A1/de not_active Ceased
- 2009-03-17 JP JP2011500107A patent/JP5695557B2/ja not_active Expired - Fee Related
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0008127A1 (de) | 1978-08-12 | 1980-02-20 | Saarbergwerke Aktiengesellschaft | Verfahren zum Verfestigen von Kohle und/oder Gestein im Bergbau |
| EP0249201A2 (en) | 1986-06-10 | 1987-12-16 | Union Carbide Corporation | High solids sag resistant cycloaliphatic epoxy coatings containing low molecular weight high Tg organic polymeric sag resisting additives |
| EP0276501A2 (en) | 1987-01-24 | 1988-08-03 | Akzo Nobel N.V. | Thickening compositions and thickened aqueous acid solutions |
| US5214086A (en) | 1991-09-04 | 1993-05-25 | Basf Corporation | Coating compositions which may be ambient cured |
| WO1994022968A1 (de) | 1993-03-31 | 1994-10-13 | Basf Lacke + Farben Ag | Nichtwässriger thixotropierter lack und verfahren zur herstellung mehrschichtiger überzüge damit |
| EP0686654A1 (en) | 1994-06-06 | 1995-12-13 | Basf Corporation | Coating compositions comprising aldimine and siocyanate and process for their preparation |
| WO1997000693A1 (en) | 1995-06-20 | 1997-01-09 | Peptide Technology Limited | Novel formulation for peptide release |
| WO1997012945A1 (en) | 1995-10-06 | 1997-04-10 | Cabot Corporation | Aqueous thixotropes for waterborne systems |
| DE69702047T2 (de) * | 1996-02-17 | 2000-10-26 | Imperial Chemical Industries Plc, London | Beschichtungszusammensetzung |
| DE102005036630B3 (de) * | 2005-08-04 | 2006-09-14 | Basf Coatings Ag | Chromfreie, zinkarme, korrosionshemmende Pigmentmischung, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE102006044035A1 (de) * | 2006-09-14 | 2008-03-27 | Basf Coatings Ag | Calciumhydrogenphosphathaltige Beschichtungszusammensetzung, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihr beschichtete Substrate |
Non-Patent Citations (13)
| Title |
|---|
| DIN 50 021 |
| DIN 50 021-SS |
| DIN 53240-2 |
| DIN EN ISO 2114 |
| DIN EN ISO 3219/A.3 |
| DIN ISO 2409 |
| Fett Wissenschaft Technologie/Fat Science Technology, 89, Seiten 147-151; J. Polym. Sci., Part B: Polym. Phys., 2003, 42, 809-819 |
| Glasurithandbuch von 1984, Vincentz Verlag, ISBN 3-87870-192-6 |
| Lückert, Pigment + Füllstofftabellen, Lückert Verlag, ISBN 3-927342-03-3 |
| March, Advanced Organic Chemistry, Reactions, Mechanisms and Structure Third ed. S. 797, John Wiley & Sons |
| Peter Volk in "Metalloberfläche", Sonderdruck 5/2006 |
| Römpp Lexikon "Lacke und Druckfarben" Georg Thieme Verlag, Stuttgart, 1998, Seiten 250 bis 252 |
| z. B. Ullmanns Enzyklopädie der technischen Chemie, 4. Auflage, Band 19, S. 62-65 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116496646A (zh) * | 2022-01-18 | 2023-07-28 | 苏州大学 | 一种超疏水光热涂层、其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US9266993B2 (en) | 2016-02-23 |
| AU2009226736B2 (en) | 2014-05-22 |
| ATE533801T1 (de) | 2011-12-15 |
| PL2271689T3 (pl) | 2012-04-30 |
| WO2009115294A1 (de) | 2009-09-24 |
| JP2011514426A (ja) | 2011-05-06 |
| EP2271689B1 (de) | 2011-11-16 |
| JP5695557B2 (ja) | 2015-04-08 |
| ES2377806T3 (es) | 2012-04-02 |
| AU2009226736A1 (en) | 2009-09-24 |
| EP2271689A1 (de) | 2011-01-12 |
| US20110020659A1 (en) | 2011-01-27 |
| MX2010009958A (es) | 2010-11-22 |
| BRPI0909670A2 (pt) | 2015-09-15 |
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