PH26839A - Aqueous-based coating compositions comprising anionic polyurethane principal resin and anionic acrylic grind resin - Google Patents
Aqueous-based coating compositions comprising anionic polyurethane principal resin and anionic acrylic grind resin Download PDFInfo
- Publication number
- PH26839A PH26839A PH40378A PH40378A PH26839A PH 26839 A PH26839 A PH 26839A PH 40378 A PH40378 A PH 40378A PH 40378 A PH40378 A PH 40378A PH 26839 A PH26839 A PH 26839A
- Authority
- PH
- Philippines
- Prior art keywords
- acid
- weight
- carboxylic acid
- resin
- basecoat
- Prior art date
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- 229920005989 resin Polymers 0.000 title claims description 105
- 239000011347 resin Substances 0.000 title claims description 105
- 239000008199 coating composition Substances 0.000 title claims description 46
- 229920002635 polyurethane Polymers 0.000 title claims description 35
- 239000004814 polyurethane Substances 0.000 title claims description 35
- 125000000129 anionic group Chemical group 0.000 title claims description 24
- 239000000203 mixture Substances 0.000 claims description 120
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 78
- 229920000728 polyester Polymers 0.000 claims description 65
- 239000002253 acid Substances 0.000 claims description 62
- 239000000049 pigment Substances 0.000 claims description 58
- 150000001875 compounds Chemical class 0.000 claims description 54
- 229920005749 polyurethane resin Polymers 0.000 claims description 46
- 238000000576 coating method Methods 0.000 claims description 43
- 239000007787 solid Substances 0.000 claims description 41
- -1 alkyl methacrylates Chemical class 0.000 claims description 40
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 39
- 239000011248 coating agent Substances 0.000 claims description 39
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 36
- 229920001225 polyester resin Polymers 0.000 claims description 33
- 239000004645 polyester resin Substances 0.000 claims description 33
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 28
- 239000007795 chemical reaction product Substances 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 27
- 239000000178 monomer Substances 0.000 claims description 27
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 24
- 239000006185 dispersion Substances 0.000 claims description 23
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 20
- 229920001228 polyisocyanate Polymers 0.000 claims description 20
- 239000005056 polyisocyanate Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 239000000539 dimer Substances 0.000 claims description 19
- 238000001035 drying Methods 0.000 claims description 19
- 238000000518 rheometry Methods 0.000 claims description 19
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 18
- 239000000758 substrate Substances 0.000 claims description 17
- 150000008065 acid anhydrides Chemical class 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 150000003141 primary amines Chemical group 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 11
- 229920003180 amino resin Polymers 0.000 claims description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
- 150000008064 anhydrides Chemical class 0.000 claims description 9
- 230000009477 glass transition Effects 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 150000001735 carboxylic acids Chemical class 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 7
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 7
- 238000004132 cross linking Methods 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 6
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims description 6
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 5
- 239000001530 fumaric acid Substances 0.000 claims description 5
- 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 5
- 239000000047 product Substances 0.000 claims description 5
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 5
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims description 5
- 239000004927 clay Substances 0.000 claims description 4
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 claims description 4
- 229910000271 hectorite Inorganic materials 0.000 claims description 4
- 238000009736 wetting Methods 0.000 claims description 4
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 3
- PGNYGWRFIFYBKV-UHFFFAOYSA-N [Mg].[Li].[Na] Chemical compound [Mg].[Li].[Na] PGNYGWRFIFYBKV-UHFFFAOYSA-N 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- 239000000391 magnesium silicate Substances 0.000 claims description 3
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 3
- 235000019792 magnesium silicate Nutrition 0.000 claims description 3
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 claims description 2
- JVYDLYGCSIHCMR-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butanoic acid Chemical compound CCC(CO)(CO)C(O)=O JVYDLYGCSIHCMR-UHFFFAOYSA-N 0.000 claims description 2
- WACQLQIAUWURGA-UHFFFAOYSA-N 3-hydroxy-2,2-bis(hydroxymethyl)propanoic acid Chemical compound OCC(CO)(CO)C(O)=O WACQLQIAUWURGA-UHFFFAOYSA-N 0.000 claims description 2
- 230000008021 deposition Effects 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims 4
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims 4
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 4
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims 2
- UHAMPPWFPNXLIU-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)pentanoic acid Chemical compound CCCC(CO)(CO)C(O)=O UHAMPPWFPNXLIU-UHFFFAOYSA-N 0.000 claims 1
- ULMZOZMSDIOZAF-UHFFFAOYSA-N 3-hydroxy-2-(hydroxymethyl)propanoic acid Chemical compound OCC(CO)C(O)=O ULMZOZMSDIOZAF-UHFFFAOYSA-N 0.000 claims 1
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 1
- 238000010348 incorporation Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 55
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 34
- 239000008367 deionised water Substances 0.000 description 24
- 229910021641 deionized water Inorganic materials 0.000 description 24
- 229920005862 polyol Polymers 0.000 description 22
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 150000003077 polyols Chemical class 0.000 description 19
- 238000010992 reflux Methods 0.000 description 19
- 238000013019 agitation Methods 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 15
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 15
- 150000002009 diols Chemical class 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 12
- 229910052618 mica group Inorganic materials 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 11
- 239000010410 layer Substances 0.000 description 11
- 239000002245 particle Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000010445 mica Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000004970 Chain extender Substances 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 9
- 229960002887 deanol Drugs 0.000 description 9
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- 229920000877 Melamine resin Polymers 0.000 description 8
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 125000005442 diisocyanate group Chemical group 0.000 description 8
- 239000012972 dimethylethanolamine Substances 0.000 description 8
- 239000012948 isocyanate Substances 0.000 description 8
- 150000002513 isocyanates Chemical class 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 229920006243 acrylic copolymer Polymers 0.000 description 7
- 150000001299 aldehydes Chemical class 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 6
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 6
- 229940117969 neopentyl glycol Drugs 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 5
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229940094522 laponite Drugs 0.000 description 5
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000011247 coating layer Substances 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 150000004668 long chain fatty acids Chemical class 0.000 description 4
- 229920005906 polyester polyol Polymers 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 150000003335 secondary amines Chemical group 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000004640 Melamine resin Substances 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000002318 adhesion promoter Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 230000000485 pigmenting effect Effects 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920003009 polyurethane dispersion Polymers 0.000 description 3
- 238000007665 sagging Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 150000003512 tertiary amines Chemical class 0.000 description 3
- 239000013638 trimer Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 229920002266 Pluriol® Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 239000001055 blue pigment Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 2
- VEIOBOXBGYWJIT-UHFFFAOYSA-N cyclohexane;methanol Chemical compound OC.OC.C1CCCCC1 VEIOBOXBGYWJIT-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000004662 dithiols Chemical class 0.000 description 2
- 229910001651 emery Inorganic materials 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
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- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000003672 ureas Chemical group 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C09D175/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/52—Two layers
- B05D7/53—Base coat plus clear coat type
- B05D7/534—Base coat plus clear coat type the first layer being let to dry at least partially before applying the second layer
-
- 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]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- 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
- Y10T428/31681—Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
-
- 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
- Y10T428/31688—Next to aldehyde or ketone condensation product
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/343,119 US4978708A (en) | 1989-04-25 | 1989-04-25 | Aqueous-based coating compositions comprising anionic polyurethane principal resin and anionic acrylic grind resin |
Publications (1)
Publication Number | Publication Date |
---|---|
PH26839A true PH26839A (en) | 1992-11-05 |
Family
ID=23344794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH40378A PH26839A (en) | 1989-04-25 | 1990-04-16 | Aqueous-based coating compositions comprising anionic polyurethane principal resin and anionic acrylic grind resin |
Country Status (11)
Country | Link |
---|---|
US (1) | US4978708A (de) |
EP (1) | EP0394737B1 (de) |
JP (1) | JP2834271B2 (de) |
KR (1) | KR0156930B1 (de) |
AR (1) | AR248038A1 (de) |
AU (1) | AU628518B2 (de) |
BR (1) | BR9001896A (de) |
CA (1) | CA2010817C (de) |
DE (1) | DE69006625T2 (de) |
NZ (1) | NZ233201A (de) |
PH (1) | PH26839A (de) |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5667847A (en) * | 1987-07-31 | 1997-09-16 | Basf Lacke+Farben Aktiengesellschaft | Process for the production of a multicoat protective and/or decorative coating and water-dilutable coating compositions |
US5275847A (en) * | 1988-09-28 | 1994-01-04 | Basf Lacke+Farben Aktiengesellschaft | Process for producing a multi-layer coating using aqueous coating compound aqueous coating compounds |
DE3936288A1 (de) * | 1989-11-01 | 1991-05-02 | Bayer Ag | In wasser dispergierbare bindemittelkombinationen, ein verfahren zur herstellung eines einbrennfuellers und dessen verwendung |
DE3942803A1 (de) * | 1989-12-23 | 1991-06-27 | Basf Lacke & Farben | Verfahren zur herstellung eines mehrschichtigen, schuetzenden und/oder dekorativen ueberzuges |
DE4009000A1 (de) * | 1990-03-21 | 1991-09-26 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen reparaturlackierung |
DE4009857A1 (de) * | 1990-03-28 | 1991-10-02 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen lackierung und fuer dieses verfahren geeignete waessrige basislacke |
DE4009931A1 (de) * | 1990-03-28 | 1991-10-02 | Basf Lacke & Farben | Verfahren zur herstellung eines mehrschichtigen ueberzugs, waessrige beschichtungszusammensetzungen, wasserverduennbare polyacrylatharze und verfahren zur herstellung von wasserverduennbaren polyacrylatharzen |
DE4011633A1 (de) * | 1990-04-11 | 1991-10-17 | Herberts Gmbh | Verfahren zur herstellung von mehrschichtueberzuegen |
JP2694225B2 (ja) * | 1990-05-21 | 1997-12-24 | 日本ペイント株式会社 | 水性塗料組成物 |
US5582949A (en) * | 1990-12-27 | 1996-12-10 | Xerox Corporation | Process for improving belts |
US5738926A (en) * | 1991-11-29 | 1998-04-14 | Diafoil Hoechst Company Limited | Metallized polyester film capacitor |
US5641829A (en) * | 1991-12-30 | 1997-06-24 | Ppg Industries, Inc. | Coating compositions prepared from base neutralized, stable aqueous dispersion of hydroxyl functional acrylic polymers |
EP0600171B1 (de) * | 1992-09-30 | 1997-01-15 | Hoechst Aktiengesellschaft | Schwerentflammbarer Teppichboden |
JP3561280B2 (ja) * | 1993-01-29 | 2004-09-02 | マツダ株式会社 | 塗装方法 |
DE4317861C1 (de) * | 1993-05-28 | 1994-11-24 | Herberts Gmbh | Verfahren zur Mehrschichtlackierung von Substraten und Anwendung des Verfahrens |
US5856404A (en) * | 1994-02-08 | 1999-01-05 | Schnee-Morehead, Inc. | Back bedding sealant composition |
DE4419216C1 (de) * | 1994-06-01 | 1995-08-31 | Bollig & Kemper | Wäßrige Überzugsmittel und deren Verwendung |
JP3727033B2 (ja) * | 1994-06-20 | 2005-12-14 | 三菱化学ポリエステルフィルム株式会社 | 昇華型感熱転写用ポリエステルフィルム |
US5968600A (en) * | 1995-09-15 | 1999-10-19 | Egyptian Lacquer Mfg. Co. | EMI/RFI-shielding coating |
US5696196A (en) * | 1995-09-15 | 1997-12-09 | Egyptian Lacquer Mfg. Co. | EMI/RFI-shielding coating |
US6057400A (en) * | 1996-06-06 | 2000-05-02 | The Sherwin-Williams Company | Waterborne basecoat compositions for use in basecoat/clearcoat applications |
US5879749A (en) * | 1997-09-16 | 1999-03-09 | National Starch And Chemical Investment Holding Corporation | Crosslinkable fabric care compositions |
ES2157732B1 (es) * | 1998-07-23 | 2002-03-01 | Akzo Nobel Coatings S A | Colorante para la fabricacion de pinturas y productos de recubrimiento de superficies y para colorear materiales en masa. |
US6204319B1 (en) | 1998-10-30 | 2001-03-20 | E.I. Du Pont De Nemours And Company | Aqueous coating compositions |
TW510916B (en) * | 1998-12-21 | 2002-11-21 | Bayer Ag | Aqueous reacitve filler compositions |
WO2000046265A1 (de) | 1999-02-03 | 2000-08-10 | Basf Coatings Ag | Polyurethan und seine verwendung in der wässrigen kunststofflackierung |
DE19908001A1 (de) | 1999-02-25 | 2000-08-31 | Basf Coatings Ag | Hochkratzfeste Mehrschichtlackierung, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE19908013A1 (de) | 1999-02-25 | 2000-08-31 | Basf Coatings Ag | Mit aktinischer Strahlung und gegebenenfalls themisch härtbare Pulverslurrys, Verfahren zu ihrer Herstellung und ihre Verwendung |
JP3961708B2 (ja) * | 1999-02-25 | 2007-08-22 | 株式会社日立製作所 | 乗客コンベア |
DE19914896A1 (de) | 1999-04-01 | 2000-10-05 | Basf Coatings Ag | Thermisch und/oder mit aktinischer Strahlung härtbarer wäßriger Beschichtungsstoff und seine Verwendung |
DE19914898C2 (de) | 1999-04-01 | 2002-10-24 | Basf Coatings Ag | Vernetzungsmittel für auf der Basis von Pyrimidin für thermisch härtbare Zusammensetzungen und deren Verwendung |
DE19920799A1 (de) | 1999-05-06 | 2000-11-16 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbarer Beschichtungsstoff und seine Verwendung |
DE19938759A1 (de) | 1999-08-16 | 2001-02-22 | Basf Coatings Ag | Beschichtungsstoff und seine Verwendung zur Herstellung hochkratzfester mehrschichtiger Klarlackierungen |
DE19940857A1 (de) | 1999-08-27 | 2001-03-01 | Basf Coatings Ag | Sol-Gel-Überzug für einschichtige oder mehrschichtige Lackierungen |
DE19944483A1 (de) | 1999-09-16 | 2001-03-29 | Basf Coatings Ag | Integriertes Lackierverfahren für Kunststoffteile enthaltende Karosserien oder Kabinen von PKW und Nutzfahrzeugen sowie deren Ersatzteile und Anbauteile |
DE19948821A1 (de) | 1999-10-09 | 2001-05-23 | Basf Coatings Ag | Elektrisch leitfähiger Hydroprimer für Kunststoffe |
US6395820B1 (en) | 1999-11-15 | 2002-05-28 | Air Products And Chemicals, Inc. | Aqueous polymer emulsion-polyester polyol blend for reducing or eliminating flooding and floating in water-based two component polyurethane coatings |
US6437036B1 (en) | 1999-11-17 | 2002-08-20 | Basf Corporation | Waterborne primer with improved chip resistance |
US6210758B1 (en) * | 1999-11-17 | 2001-04-03 | Basf Corporation | Composite coating with improved chip resistance |
US6342558B1 (en) | 1999-11-17 | 2002-01-29 | Basf Corporation | Waterborne primer with improved chip resistance |
DE10008946C1 (de) | 2000-02-25 | 2001-10-18 | Basf Coatings Ag | Verfahren zur Herstellung farb- und/oder effektgebender Mehrschichtlackierungen auf Automobilkarosserien |
US6384131B1 (en) | 2000-05-01 | 2002-05-07 | The Sherwin-Williams Company | Waterborne basecoat compositions for use in basecoat/clearcoat applications |
DE10043405C1 (de) | 2000-09-04 | 2002-06-27 | Basf Coatings Ag | Verfahren zur Herstellung farb- und/oder effektgebender Lackierungen |
JP2002086625A (ja) * | 2000-09-19 | 2002-03-26 | Dainippon Printing Co Ltd | 化粧板 |
DE10100195A1 (de) | 2001-01-04 | 2002-08-01 | Basf Coatings Ag | Wäßriger, effektgebender Beschichtungsstoff, Verfahren zu seiner Herstellung und seine Verwendung |
US6518338B2 (en) | 2001-05-08 | 2003-02-11 | Basf Corporation | Fast drying alkyd basecoat refinish composition |
US6794442B2 (en) | 2001-06-21 | 2004-09-21 | Basf Corporation | Fast drying basecoat refinish composition |
DE10130972C1 (de) | 2001-06-27 | 2002-11-07 | Basf Coatings Ag | Verfahren zur Herstellung von Beschichtungen aus thermisch und mit aktinischer Strahlung härtbaren Beschichtungsstoffen und mit dem Verfahren herstellbare Lackierungen |
JP4186002B2 (ja) * | 2001-10-31 | 2008-11-26 | 学校法人日本大学 | 樹脂組成物およびそれを用いた熱可塑性樹脂積層体とそれらの製造方法 |
CN1891352B (zh) * | 2001-11-29 | 2011-03-02 | 本田加拿多有限公司 | 用于含有白色珠光涂料制剂的白色颜料 |
US20030134970A1 (en) * | 2002-01-17 | 2003-07-17 | Basf Corporation | Basecoat coating composition having low volatile organic content and composite coating prepared therefrom |
DE10206225C1 (de) * | 2002-02-15 | 2003-09-18 | Basf Coatings Ag | Verfahren zur Herstellung farb- und/oder effektgebender Mehrschichtlackierungen |
US7052541B2 (en) * | 2002-06-19 | 2006-05-30 | Board Of Regents, The University Of Texas System | Color compositions |
CN100345872C (zh) * | 2002-09-18 | 2007-10-31 | 威士伯来源有限公司 | 可自交联的水基涂料组合物 |
DE502004007096D1 (de) | 2003-02-24 | 2008-06-19 | Basf Se | Polymere enthaltend Phosphor- und/oder Phosphonsäure Gruppen zur Metalloberflächenbehandlung |
EP1522352B1 (de) * | 2003-10-10 | 2006-06-21 | Rohm And Haas Company | Grundierungsfreie Beschichtung von wärmeempfindlichen Substraten und Beschichtungsstrasse |
US7425235B2 (en) | 2005-02-11 | 2008-09-16 | The Board Of Regents Of The University Of Texas System | Color compositions and methods of manufacture |
JP5116002B2 (ja) * | 2005-03-17 | 2013-01-09 | 株式会社リコー | 水系顔料分散体の製造方法、水系顔料インクの製造方法、及び該インクを用いたインクカートリッジ、インクジェット記録装置、画像形成方法、それによる画像形成物 |
DE102005012589B4 (de) | 2005-03-18 | 2007-06-14 | Basf Coatings Ag | Mit UV-A-Strahlung härtbares, lösemittelhaltiges Gemisch, Verfahren zu seiner Herstellung und seine Verwendung |
CA2615514A1 (en) * | 2005-06-17 | 2006-12-28 | The Board Of Regents Of The University Of Texas System | Organic/inorganic lewis acid composite materials |
CA2612889C (en) * | 2005-07-01 | 2011-06-28 | The Sherwin-Williams Company | Multi-layer coating system including a hydroxyl modified polyurethane dispersion binder |
US7632570B2 (en) * | 2006-09-20 | 2009-12-15 | Ppg Industries Ohio, Inc. | Aqueous resinous binders |
US7736744B2 (en) * | 2006-09-20 | 2010-06-15 | Ppg Industries Ohio, Inc. | Aqueous resinous binders |
DE102007031594A1 (de) | 2007-07-06 | 2009-01-08 | Basf Coatings Ag | Universeller Spotblender für Einkomponenten- und Zweikomponentenklarlacke |
EA023159B1 (ru) * | 2010-01-13 | 2016-04-29 | Пазкар Лтд. | Двухкомпонентные полиуретановые композиции и покрытия на водной основе |
WO2014026780A1 (en) | 2012-08-16 | 2014-02-20 | Basf Coatings Gmbh | Coating compositions containing benzotrizol based uv-absorbers |
US9522413B2 (en) * | 2013-02-28 | 2016-12-20 | Ppg Industries Ohio, Inc. | Methods and compositions for coating substrates |
PL3083077T3 (pl) * | 2013-12-18 | 2020-04-30 | Basf Coatings Gmbh | Sposób wytwarzania wielowarstwowej powłoki lakierniczej |
DE102014007805A1 (de) | 2014-05-27 | 2015-12-03 | WindplusSonne GmbH | Solarabsorber, Verfahren zu seiner Herstellung und seine Verwendung |
DE102014013600A1 (de) | 2014-09-13 | 2016-03-17 | WindplusSonne GmbH | Solarabsorber, Verfahren zu seiner Herstellung und seine Verwendung |
DE102018207815A1 (de) | 2018-05-18 | 2019-11-21 | Karl Wörwag Lack- Und Farbenfabrik Gmbh & Co. Kg | Mehrschichtige, farb- und/oder effektgebende Lackierung sowie Verfahren zur Bildung einer Basislackschicht |
CN112376291A (zh) * | 2020-11-02 | 2021-02-19 | 吴江市斌缘纺织喷绘材料有限公司 | 一种水性纺织涂层的制备方法 |
JP7088324B2 (ja) * | 2021-01-04 | 2022-06-21 | 三菱ケミカル株式会社 | プライマー組成物及びこれを用いてなる水性液、プライマー層付き基材フィルム並びにプリズムシート |
CN113150257B (zh) * | 2021-02-26 | 2023-06-13 | 南雄市三本化学科技有限公司 | 一种聚酯树脂及其制备方法和在湿碰湿工艺中的应用 |
CN113061373A (zh) * | 2021-04-01 | 2021-07-02 | 萍乡明鑫电瓷成套有限公司 | 一种防污型盘形悬式瓷绝缘子制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4007306A (en) * | 1974-11-26 | 1977-02-08 | Inmont Corporation | Method of applying aqueous coating compositions |
DE3545618A1 (de) * | 1985-12-21 | 1987-06-25 | Basf Lacke & Farben | Wasserverduennbares ueberzugsmittel zur herstellung der basisschicht eines mehrschichtueberzuges |
DE3704350A1 (de) * | 1987-02-12 | 1988-08-25 | Henkel Kgaa | Wasserverduennbare ueberzugsmittel |
US4791168A (en) * | 1987-04-15 | 1988-12-13 | Basf Corporation, Inmont Division | Polyurethane resins in water-dilutable basecoats having low flash and quick-drying characteristics |
US4794147A (en) * | 1987-07-24 | 1988-12-27 | Basf Corporation, Inmont Division | Novel non-ionic polyurethane resins having polyether backbones in water-dilutable basecoats |
US5017673A (en) * | 1989-10-12 | 1991-05-21 | Basf Corporation | Nonionically stabilized polyester urethane resin for water-borne coating compositions |
-
1989
- 1989-04-25 US US07/343,119 patent/US4978708A/en not_active Expired - Lifetime
-
1990
- 1990-02-23 CA CA002010817A patent/CA2010817C/en not_active Expired - Lifetime
- 1990-04-04 NZ NZ233201A patent/NZ233201A/xx unknown
- 1990-04-09 EP EP90106792A patent/EP0394737B1/de not_active Expired - Lifetime
- 1990-04-09 DE DE69006625T patent/DE69006625T2/de not_active Expired - Fee Related
- 1990-04-16 PH PH40378A patent/PH26839A/en unknown
- 1990-04-19 KR KR1019900005489A patent/KR0156930B1/ko not_active IP Right Cessation
- 1990-04-20 AU AU53724/90A patent/AU628518B2/en not_active Ceased
- 1990-04-20 JP JP2105105A patent/JP2834271B2/ja not_active Expired - Fee Related
- 1990-04-23 AR AR90316696A patent/AR248038A1/es active
- 1990-04-24 BR BR909001896A patent/BR9001896A/pt unknown
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EP0394737A1 (de) | 1990-10-31 |
AU5372490A (en) | 1990-11-01 |
US4978708A (en) | 1990-12-18 |
NZ233201A (en) | 1991-11-26 |
JPH0372581A (ja) | 1991-03-27 |
BR9001896A (pt) | 1991-07-30 |
EP0394737B1 (de) | 1994-02-16 |
KR0156930B1 (ko) | 1999-02-01 |
DE69006625D1 (de) | 1994-03-24 |
DE69006625T2 (de) | 1994-09-15 |
JP2834271B2 (ja) | 1998-12-09 |
AR248038A1 (es) | 1995-05-31 |
CA2010817C (en) | 2001-01-30 |
AU628518B2 (en) | 1992-09-17 |
CA2010817A1 (en) | 1990-10-25 |
KR900016404A (ko) | 1990-11-13 |
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