MXPA02000875A - Composicion de revestimiento de dos componentes y metodo de preparacion. - Google Patents
Composicion de revestimiento de dos componentes y metodo de preparacion.Info
- Publication number
- MXPA02000875A MXPA02000875A MXPA02000875A MXPA02000875A MXPA02000875A MX PA02000875 A MXPA02000875 A MX PA02000875A MX PA02000875 A MXPA02000875 A MX PA02000875A MX PA02000875 A MXPA02000875 A MX PA02000875A MX PA02000875 A MXPA02000875 A MX PA02000875A
- Authority
- MX
- Mexico
- Prior art keywords
- polymer
- percent
- weight
- functional group
- acrylate
- Prior art date
Links
- 239000008199 coating composition Substances 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims description 37
- 238000002360 preparation method Methods 0.000 title description 16
- 229920000642 polymer Polymers 0.000 claims abstract description 204
- 239000000203 mixture Substances 0.000 claims abstract description 105
- 125000000524 functional group Chemical group 0.000 claims abstract description 61
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 14
- 125000002843 carboxylic acid group Chemical group 0.000 claims abstract 3
- 239000000178 monomer Substances 0.000 claims description 74
- 239000003431 cross linking reagent Substances 0.000 claims description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- 239000002253 acid Substances 0.000 claims description 22
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 21
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 21
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 21
- 229910021645 metal ion Inorganic materials 0.000 claims description 18
- 150000001718 carbodiimides Chemical class 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 15
- 125000004069 aziridinyl group Chemical group 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 11
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- 239000002585 base Substances 0.000 claims description 10
- 125000003700 epoxy group Chemical group 0.000 claims description 9
- 150000002513 isocyanates Chemical class 0.000 claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 8
- 150000003573 thiols Chemical class 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 7
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 6
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000001993 wax Substances 0.000 claims description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 238000004132 cross linking Methods 0.000 claims description 3
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 2
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 2
- WWJCRUKUIQRCGP-UHFFFAOYSA-N 3-(dimethylamino)propyl 2-methylprop-2-enoate Chemical compound CN(C)CCCOC(=O)C(C)=C WWJCRUKUIQRCGP-UHFFFAOYSA-N 0.000 claims description 2
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims description 2
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims description 2
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 2
- 238000000576 coating method Methods 0.000 abstract description 33
- 239000005056 polyisocyanate Substances 0.000 abstract description 24
- 229920001228 polyisocyanate Polymers 0.000 abstract description 24
- 239000011248 coating agent Substances 0.000 abstract description 22
- 239000004971 Cross linker Substances 0.000 abstract description 8
- 238000005498 polishing Methods 0.000 description 71
- 238000012360 testing method Methods 0.000 description 50
- 239000007787 solid Substances 0.000 description 35
- 239000000839 emulsion Substances 0.000 description 33
- 238000009472 formulation Methods 0.000 description 28
- -1 acrylate ester Chemical class 0.000 description 27
- 239000003599 detergent Substances 0.000 description 21
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 20
- 230000000052 comparative effect Effects 0.000 description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 14
- 239000011777 magnesium Substances 0.000 description 14
- 239000004908 Emulsion polymer Substances 0.000 description 11
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 10
- 230000006866 deterioration Effects 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000012423 maintenance Methods 0.000 description 9
- 238000010998 test method Methods 0.000 description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 5
- 229910052749 magnesium Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 238000007720 emulsion polymerization reaction Methods 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000008034 disappearance Effects 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 238000007790 scraping Methods 0.000 description 3
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical group CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical class OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 206010049155 Visual brightness Diseases 0.000 description 2
- 229920004482 WACKER® Polymers 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 210000000282 nail Anatomy 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- SVZNRBAZGGBJOW-UHFFFAOYSA-N (2-methylprop-2-enoylamino)methanesulfonic acid Chemical compound CC(=C)C(=O)NCS(O)(=O)=O SVZNRBAZGGBJOW-UHFFFAOYSA-N 0.000 description 1
- POTYORUTRLSAGZ-UHFFFAOYSA-N (3-chloro-2-hydroxypropyl) prop-2-enoate Chemical compound ClCC(O)COC(=O)C=C POTYORUTRLSAGZ-UHFFFAOYSA-N 0.000 description 1
- KKSNTCYLMGYFFB-UHFFFAOYSA-N (prop-2-enoylamino)methanesulfonic acid Chemical compound OS(=O)(=O)CNC(=O)C=C KKSNTCYLMGYFFB-UHFFFAOYSA-N 0.000 description 1
- VNMOIBZLSJDQEO-UHFFFAOYSA-N 1,10-diisocyanatodecane Chemical compound O=C=NCCCCCCCCCCN=C=O VNMOIBZLSJDQEO-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 description 1
- LFKLPJRVSHJZPL-UHFFFAOYSA-N 1,2:7,8-diepoxyoctane Chemical compound C1OC1CCCCC1CO1 LFKLPJRVSHJZPL-UHFFFAOYSA-N 0.000 description 1
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- GNQKHBSIBXSFFD-UHFFFAOYSA-N 1,3-diisocyanatocyclohexane Chemical compound O=C=NC1CCCC(N=C=O)C1 GNQKHBSIBXSFFD-UHFFFAOYSA-N 0.000 description 1
- FRCWRQFTQTWNKQ-UHFFFAOYSA-N 1,4-diisocyanatobut-1-ene Chemical class O=C=NCCC=CN=C=O FRCWRQFTQTWNKQ-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- SSZOCHFYWWVSAI-UHFFFAOYSA-N 1-bromo-2-ethenylbenzene Chemical compound BrC1=CC=CC=C1C=C SSZOCHFYWWVSAI-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- NSOAQRMLVFRWIT-UHFFFAOYSA-N 1-ethenoxydecane Chemical compound CCCCCCCCCCOC=C NSOAQRMLVFRWIT-UHFFFAOYSA-N 0.000 description 1
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 1
- HWRMMWBUMQCMJK-UHFFFAOYSA-N 1-ethenylsulfanylpropane Chemical compound CCCSC=C HWRMMWBUMQCMJK-UHFFFAOYSA-N 0.000 description 1
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
- WAGRIKSHWXFXHV-UHFFFAOYSA-N 1-hydroxybutyl prop-2-enoate Chemical compound CCCC(O)OC(=O)C=C WAGRIKSHWXFXHV-UHFFFAOYSA-N 0.000 description 1
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
- WULAHPYSGCVQHM-UHFFFAOYSA-N 2-(2-ethenoxyethoxy)ethanol Chemical compound OCCOCCOC=C WULAHPYSGCVQHM-UHFFFAOYSA-N 0.000 description 1
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 1
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- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- POSICDHOUBKJKP-UHFFFAOYSA-N prop-2-enoxybenzene Chemical compound C=CCOC1=CC=CC=C1 POSICDHOUBKJKP-UHFFFAOYSA-N 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical group CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical group CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 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
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/06—Other polishing compositions
- C09G1/14—Other polishing compositions based on non-waxy substances
- C09G1/16—Other polishing compositions based on non-waxy substances on natural or synthetic resins
-
- 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
- C08G18/703—Isocyanates or isothiocyanates transformed in a latent form by physical means
- C08G18/705—Dispersions of isocyanates or isothiocyanates in a liquid medium
- C08G18/706—Dispersions of isocyanates or isothiocyanates in a liquid medium the liquid medium being water
-
- 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
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/066—Copolymers with monomers not covered by C09D133/06 containing -OH groups
-
- 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)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26496201P | 2001-01-30 | 2001-01-30 | |
| US30609601P | 2001-07-17 | 2001-07-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02000875A true MXPA02000875A (es) | 2002-09-18 |
Family
ID=26950854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02000875A MXPA02000875A (es) | 2001-01-30 | 2002-01-24 | Composicion de revestimiento de dos componentes y metodo de preparacion. |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US6875834B2 (enExample) |
| EP (1) | EP1227116B1 (enExample) |
| JP (1) | JP2002302640A (enExample) |
| CN (1) | CN1239647C (enExample) |
| AU (1) | AU784341B2 (enExample) |
| BR (1) | BR0200311A (enExample) |
| DE (1) | DE60210214T2 (enExample) |
| ES (1) | ES2261597T3 (enExample) |
| MX (1) | MXPA02000875A (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7763354B2 (en) * | 2002-09-17 | 2010-07-27 | Ppg Industries Ohio, Inc. | Waterborne 2k coating composition having good pot life |
| US8389113B2 (en) | 2002-09-17 | 2013-03-05 | Ppg Industries Ohio, Inc. | Substrates and articles of manufacture coated with a waterborne 2K coating composition |
| US7285590B2 (en) * | 2003-11-13 | 2007-10-23 | Hexion Specialty Chemicals, Inc. | Aqueous dispersions containing multi-stage emulsion polymers |
| US20050153139A1 (en) * | 2004-01-12 | 2005-07-14 | Levitt Mark D. | Aqueous polyurethane coating system containing zinc crosslinked acrylic dispersion |
| US7655718B2 (en) * | 2004-01-12 | 2010-02-02 | Ecolab Inc. | Polyurethane coating cure enhancement using zinc carbonate initiators |
| US8128998B2 (en) * | 2004-01-12 | 2012-03-06 | Ecolab Usa Inc. | Polyurethane coating cure enhancement using ultrafine zinc oxide |
| WO2005071029A2 (en) * | 2004-01-12 | 2005-08-04 | Ecolab Inc. | Polyurethane coating system containing zinc initiator |
| EP1634900B1 (en) * | 2004-09-10 | 2007-10-31 | Rohm and Haas Company | Durable two-part polyurethane floor coating |
| US20070148357A1 (en) * | 2005-10-03 | 2007-06-28 | The Sherwin-Williams Company | Fast Hardening Aqueous Coating Composition |
| JP4542024B2 (ja) * | 2005-11-24 | 2010-09-08 | Ｓｒｉスポーツ株式会社 | 塗装ゴルフボール及びその製造方法 |
| KR20080107394A (ko) * | 2006-01-26 | 2008-12-10 | 알렉잔더 딘 워로넉 | 일시적 보호 폴리머 코팅 및 제거 시스템 |
| US7730761B2 (en) * | 2006-06-16 | 2010-06-08 | Rohm And Haas Company | Producing stress on surfaces |
| JP5491865B2 (ja) * | 2007-03-22 | 2014-05-14 | 関西ペイント株式会社 | 水性塗料組成物及び複層塗膜形成方法 |
| CN101125998B (zh) * | 2007-09-29 | 2010-12-22 | 佛山市顺德区华隆涂料实业有限公司 | 金属交联分子成膜双组分水性木器漆及其制备方法 |
| JP5406490B2 (ja) * | 2008-09-19 | 2014-02-05 | 株式会社ユーホーニイタカ | フロアーポリッシュ組成物 |
| WO2012082622A1 (en) * | 2010-12-17 | 2012-06-21 | Rohm And Haas Company | Restrippable photovoltaic coatings |
| CN103183766B (zh) * | 2011-12-29 | 2016-06-08 | 德谦（上海）化学有限公司 | 适用于双组份聚氨酯铝粉漆的丙烯酸树脂 |
| CN110655871A (zh) | 2012-01-25 | 2020-01-07 | 欧美诺华解决方案公司 | 含有硅烷基团的聚合物组合物和含有其的涂层 |
| BR112014018948A8 (pt) * | 2012-02-28 | 2017-07-11 | Rohm & Haas | Composição de revestimento de piso e método para proteger um substrato de piso tendo uma superfície |
| WO2013174894A1 (en) | 2012-05-24 | 2013-11-28 | Basf Se | Aqueous binder compositions |
| US11535762B2 (en) | 2012-09-18 | 2022-12-27 | Ennis Flint | Fast drying aqueous amine free coating composition(s) |
| US9868313B2 (en) * | 2012-12-28 | 2018-01-16 | Avery Dennison Corporation | Topcoat compositions, coated substrates, and related methods |
| CN103254706A (zh) * | 2013-05-21 | 2013-08-21 | 佛山市皇冠化工有限公司 | 一种水性离型剂及其制备方法 |
| US20150190844A1 (en) * | 2013-10-15 | 2015-07-09 | Diversey, Inc. | System and Method for Preparing and Maintaining a Hard Surface |
| CN106103616B (zh) * | 2014-03-24 | 2018-11-09 | 罗门哈斯公司 | 环氧树脂-强化的地板抛光剂 |
| CN103980771B (zh) * | 2014-06-10 | 2016-03-16 | 马鞍山创宁新材料科技有限公司 | 一种纳米改性的水基多功能吸音涂料及其制备方法 |
| JP2016017116A (ja) * | 2014-07-07 | 2016-02-01 | スリーエム イノベイティブ プロパティズ カンパニー | 床用コーティング剤 |
| US9907449B2 (en) | 2015-03-16 | 2018-03-06 | Irobot Corporation | Autonomous floor cleaning with a removable pad |
| US9265396B1 (en) | 2015-03-16 | 2016-02-23 | Irobot Corporation | Autonomous floor cleaning with removable pad |
| WO2017040662A1 (en) | 2015-08-31 | 2017-03-09 | Diversey, Inc. | Alcohol-resistant, chemically-strippable floor coating and composition for making same |
| JP6849699B2 (ja) * | 2016-04-29 | 2021-03-24 | ダウ グローバル テクノロジーズ エルエルシー | 多層コーティングおよびその多層コーティングの調製プロセス |
| CN107163743B (zh) * | 2017-07-14 | 2019-06-25 | 广东伊思曼新材料科技股份有限公司 | 一种集装厢辊涂用水性木器地板漆及其制备方法 |
| US20190379010A1 (en) * | 2018-06-08 | 2019-12-12 | Cyberx Engineering Inc. | Flexible batteries |
| CN112469741A (zh) | 2018-07-05 | 2021-03-09 | 巴斯夫欧洲公司 | 制备水性聚合物分散体的方法 |
| JP7305754B2 (ja) * | 2018-09-28 | 2023-07-10 | ダウ グローバル テクノロジーズ エルエルシー | 水性ポリマー分散液およびそれを含む水性コーティング組成物 |
| FI3966260T3 (fi) | 2019-05-08 | 2023-06-21 | Basf Se | Vesipitoinen polymeerilateksi |
| US12365755B2 (en) * | 2019-10-29 | 2025-07-22 | Dow Global Technologies Llc | Two-component polyurethane composition |
| WO2021148565A1 (en) | 2020-01-22 | 2021-07-29 | Covestro (Netherlands) B.V. | Aziridinyl functional compound |
| WO2021171150A1 (en) * | 2020-02-28 | 2021-09-02 | Diversey, Inc. | Floor finishing compositions with enhanced durability, methods of making and using thereof |
| CN113861844A (zh) * | 2020-06-30 | 2021-12-31 | 科思创德国股份有限公司 | 一种水性涂料组合物 |
| WO2022018013A1 (en) | 2020-07-20 | 2022-01-27 | Basf Se | Aqueous polymer latex of film-forming copolymers suitable as binder in waterborne coating compositions |
| KR20230084224A (ko) * | 2020-10-05 | 2023-06-12 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 코팅 조성물의 저온 경화를 위한 고 전달 효율 적용 방법 및 그에 의해 형성된 코팅된 기판 |
| EP4284844A1 (en) | 2021-01-26 | 2023-12-06 | Basf Se | Aqueous polymer latex |
| CN117794992A (zh) | 2021-08-04 | 2024-03-29 | 巴斯夫欧洲公司 | 用于对水性聚合物胶乳进行改性方法 |
| EP4413087A1 (en) | 2021-10-04 | 2024-08-14 | Basf Se | Use of aqueous polymer compositions as stains for porous materials |
| TW202432614A (zh) | 2022-11-18 | 2024-08-16 | 德商巴斯夫歐洲公司 | 適合作為水基性塗料組成物中之黏結劑之成膜共聚物之水性聚合物乳膠 |
| TW202502831A (zh) | 2023-03-24 | 2025-01-16 | 德商巴斯夫歐洲公司 | 適合作為水性塗料組成物中黏合劑的成膜共聚物的水性聚合物膠乳 |
| TW202509091A (zh) | 2023-08-16 | 2025-03-01 | 德商巴斯夫歐洲公司 | 適合作為水性塗料組成物中之黏合劑之共聚物之含水聚合物乳膠 |
| WO2025125496A1 (en) | 2023-12-13 | 2025-06-19 | Basf Se | Aqueous polymer latex of copolymers suitable as binder in waterborne coating compositions |
| WO2025132646A1 (en) | 2023-12-19 | 2025-06-26 | Basf Se | Waterborne coating compositions requiring reduced amounts of biocides |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4150005A (en) | 1977-03-17 | 1979-04-17 | Rohm And Haas Company | Internally plasticized polymer latex |
| JPS6172071A (ja) | 1984-09-17 | 1986-04-14 | Yuuhoo Chem Kk | 被覆剤組成物 |
| JPH083077B2 (ja) * | 1987-03-30 | 1996-01-17 | 日本合成ゴム株式会社 | 艶だし用組成物 |
| WO1989010380A1 (en) | 1988-04-18 | 1989-11-02 | S.C. Johnson & Son, Inc. | Water-dispersable polyurethane/acrylic polymer compositions |
| DE3829587A1 (de) | 1988-09-01 | 1990-03-15 | Bayer Ag | Beschichtungsmittel, ein verfahren zu ihrer herstellung und die verwendung von ausgewaehlten zweikomponenten-polyurethansystemen als bindemittel fuer derartige beschichtungsmittel |
| US5051464A (en) | 1989-09-01 | 1991-09-24 | E. I. Du Pont De Nemours And Company | Waterborne acrylourethane pigment dispersant polymer |
| EP0523993A1 (en) | 1991-07-17 | 1993-01-20 | Cargill, Incorporated | Acrylic polymer aqueous dispersion with co-solvent |
| DE4136618A1 (de) | 1991-11-07 | 1993-05-13 | Bayer Ag | Wasserdispergierbare polyisocyanatgemische |
| DE4137429A1 (de) * | 1991-11-14 | 1993-05-19 | Bayer Ag | Waessrige bindemittelkombination, ein verfahren zu ihrer herstellung und ihre verwendung |
| DE4322242A1 (de) * | 1993-07-03 | 1995-01-12 | Basf Lacke & Farben | Wäßriges Zweikomponenten-Polyurethan-Beschichtungsmittel, Verfahren zu seiner Herstellung und seine Verwendung in Verfahren zur Hestellung einer Mehrschichtlackierung |
| DE4332322A1 (de) | 1993-09-23 | 1995-03-30 | Bayer Ag | Wasserlösliche bzw. -dispergierbare Polyisocyanat-Zubereitung |
| JPH0892529A (ja) | 1994-09-20 | 1996-04-09 | Yuho Chem Kk | フロアーポリッシュ用組成物 |
| US20020002235A1 (en) | 1995-04-28 | 2002-01-03 | Mathieu Joanicot | Latex dispersions containing a hydroxyl functional group and a carboxylic functional group and their use for the manufacture of coatings |
| FR2733506B1 (fr) * | 1995-04-28 | 1997-06-06 | Rhone Poulenc Chimie | Dispersions de latex a fonction hydroxyle et a fonction carboxylique et leur utilisation pour fabrication des revetements |
| JP2000086977A (ja) | 1998-09-16 | 2000-03-28 | Yuho Chem Kk | フロアーポリッシュ組成物 |
-
2002
- 2002-01-16 US US10/050,199 patent/US6875834B2/en not_active Expired - Fee Related
- 2002-01-17 AU AU10226/02A patent/AU784341B2/en not_active Ceased
- 2002-01-18 ES ES02250349T patent/ES2261597T3/es not_active Expired - Lifetime
- 2002-01-18 EP EP02250349A patent/EP1227116B1/en not_active Expired - Lifetime
- 2002-01-18 DE DE60210214T patent/DE60210214T2/de not_active Expired - Fee Related
- 2002-01-22 CN CN02102453.7A patent/CN1239647C/zh not_active Expired - Fee Related
- 2002-01-24 MX MXPA02000875A patent/MXPA02000875A/es active IP Right Grant
- 2002-01-29 BR BR0200311-2A patent/BR0200311A/pt active Search and Examination
- 2002-01-30 JP JP2002021250A patent/JP2002302640A/ja active Pending
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2005
- 2005-02-03 US US11/050,271 patent/US7396891B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US6875834B2 (en) | 2005-04-05 |
| AU784341B2 (en) | 2006-03-16 |
| AU1022602A (en) | 2002-08-01 |
| US20050137335A1 (en) | 2005-06-23 |
| JP2002302640A (ja) | 2002-10-18 |
| DE60210214D1 (de) | 2006-05-18 |
| CN1239647C (zh) | 2006-02-01 |
| EP1227116A1 (en) | 2002-07-31 |
| US7396891B2 (en) | 2008-07-08 |
| ES2261597T3 (es) | 2006-11-16 |
| EP1227116B1 (en) | 2006-03-29 |
| DE60210214T2 (de) | 2006-11-02 |
| BR0200311A (pt) | 2002-10-29 |
| US20020183455A1 (en) | 2002-12-05 |
| CN1368524A (zh) | 2002-09-11 |
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