CA2185637A1 - Method of producing wear resistant traffic markings - Google Patents
Method of producing wear resistant traffic markingsInfo
- Publication number
- CA2185637A1 CA2185637A1 CA002185637A CA2185637A CA2185637A1 CA 2185637 A1 CA2185637 A1 CA 2185637A1 CA 002185637 A CA002185637 A CA 002185637A CA 2185637 A CA2185637 A CA 2185637A CA 2185637 A1 CA2185637 A1 CA 2185637A1
- Authority
- CA
- Canada
- Prior art keywords
- latex binder
- binder
- water
- traffic
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 59
- 239000004816 latex Substances 0.000 claims abstract description 132
- 229920000126 latex Polymers 0.000 claims abstract description 132
- 239000011230 binding agent Substances 0.000 claims abstract description 126
- 239000000203 mixture Substances 0.000 claims abstract description 125
- 229920000642 polymer Polymers 0.000 claims abstract description 82
- 239000003973 paint Substances 0.000 claims abstract description 77
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 claims abstract description 28
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000001412 amines Chemical class 0.000 claims description 70
- 239000000178 monomer Substances 0.000 claims description 50
- 239000007787 solid Substances 0.000 claims description 48
- 239000002245 particle Substances 0.000 claims description 45
- -1 R2 is either H Chemical group 0.000 claims description 36
- 239000002253 acid Substances 0.000 claims description 27
- 239000011521 glass Substances 0.000 claims description 27
- 239000011324 bead Substances 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 16
- 239000000701 coagulant Substances 0.000 claims description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 14
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 14
- 150000002081 enamines Chemical class 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 claims description 8
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 7
- 229910021529 ammonia Inorganic materials 0.000 claims description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 4
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical group CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 3
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-UHFFFAOYSA-N 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 239000011976 maleic acid Substances 0.000 claims description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims description 2
- XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 claims description 2
- SWDDLRSGGCWDPH-UHFFFAOYSA-N 4-triethoxysilylbutan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCCN SWDDLRSGGCWDPH-UHFFFAOYSA-N 0.000 claims description 2
- WIVTXBIFTLNVCZ-UHFFFAOYSA-N CC(=C)C(=O)OCCP(=O)=O Chemical compound CC(=C)C(=O)OCCP(=O)=O WIVTXBIFTLNVCZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 claims description 2
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 claims description 2
- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 claims description 2
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 230000000379 polymerizing effect Effects 0.000 claims 2
- YHSYGCXKWUUKIK-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C=C YHSYGCXKWUUKIK-UHFFFAOYSA-N 0.000 claims 1
- FHPDNLOSEWLERE-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCCOC(=O)C(C)=C FHPDNLOSEWLERE-UHFFFAOYSA-N 0.000 claims 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims 1
- FDXNZIIASVNQSJ-UHFFFAOYSA-N [3-(2-methylprop-2-enoyloxy)-2-(3-oxobutanoyloxy)propyl] 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC(COC(=O)C(C)=C)OC(=O)CC(C)=O FDXNZIIASVNQSJ-UHFFFAOYSA-N 0.000 claims 1
- NHBRUUFBSBSTHM-UHFFFAOYSA-N n'-[2-(3-trimethoxysilylpropylamino)ethyl]ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCNCCN NHBRUUFBSBSTHM-UHFFFAOYSA-N 0.000 claims 1
- HGPTXDZDJMMSOP-UHFFFAOYSA-N n'-[3-[dimethoxy(methyl)silyl]propyl]ethane-1,2-diamine;n-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCCC[Si](OC)(OC)OC.CO[Si](C)(OC)CCCNCCN HGPTXDZDJMMSOP-UHFFFAOYSA-N 0.000 claims 1
- DVYVMJLSUSGYMH-UHFFFAOYSA-N n-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCCC[Si](OC)(OC)OC DVYVMJLSUSGYMH-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 134
- 229910001868 water Inorganic materials 0.000 description 56
- 238000012360 testing method Methods 0.000 description 29
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 21
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 16
- 239000000243 solution Substances 0.000 description 14
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 12
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 10
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 10
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 10
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 10
- 235000010350 erythorbic acid Nutrition 0.000 description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 10
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 10
- 229940026239 isoascorbic acid Drugs 0.000 description 10
- 229920000768 polyamine Polymers 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 9
- 239000012299 nitrogen atmosphere Substances 0.000 description 9
- 229920003169 water-soluble polymer Polymers 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000008199 coating composition Substances 0.000 description 6
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000008947 Amm Methods 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 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 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 3
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 3
- 239000001099 ammonium carbonate Substances 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 3
- 239000003981 vehicle Substances 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
- UNFLSUWOIKQTGW-UHFFFAOYSA-N 1-aminosilylbutane-1,3-dione Chemical compound CC(=O)CC(=O)[SiH2]N UNFLSUWOIKQTGW-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-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
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- 101100244083 Arabidopsis thaliana PKL gene Proteins 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 241001441571 Hiodontidae Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
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- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000012986 chain transfer agent Substances 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000008385 outer phase Substances 0.000 description 2
- 125000000913 palmityl 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])[H] 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000006254 rheological additive Substances 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
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- 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 1
- 238000003860 storage Methods 0.000 description 1
- 201000009032 substance abuse Diseases 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GEKDEMKPCKTKEC-UHFFFAOYSA-N tetradecane-1-thiol Chemical compound CCCCCCCCCCCCCCS GEKDEMKPCKTKEC-UHFFFAOYSA-N 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent 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
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/004—Reflecting paints; Signal paints
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing 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
- 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
-
- 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]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
-
- 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]
- Y10T428/31855—Of addition polymer from unsaturated monomers
-
- 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
- Y10T428/4935—Impregnated naturally solid product [e.g., leather, stone, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Road Repair (AREA)
- Road Signs Or Road Markings (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Road Paving Structures (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US420195P | 1995-09-22 | 1995-09-22 | |
| US60/004,201 | 1995-09-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2185637A1 true CA2185637A1 (en) | 1997-03-23 |
Family
ID=21709657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002185637A Abandoned CA2185637A1 (en) | 1995-09-22 | 1996-09-16 | Method of producing wear resistant traffic markings |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US5672379A (https=) |
| EP (1) | EP0764699B1 (https=) |
| JP (1) | JP4107691B2 (https=) |
| CN (1) | CN1070900C (https=) |
| AU (1) | AU701280B2 (https=) |
| CA (1) | CA2185637A1 (https=) |
| DE (1) | DE69625146T2 (https=) |
| MX (1) | MX9604188A (https=) |
| NZ (1) | NZ299341A (https=) |
| SG (1) | SG68592A1 (https=) |
| TW (1) | TW353110B (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117355573A (zh) * | 2021-06-21 | 2024-01-05 | 罗门哈斯公司 | 成膜性和非成膜性聚合物颗粒的水性分散体 |
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| CA2210807A1 (en) | 1995-01-18 | 1996-07-25 | The Dow Chemical Company | Fast hardening aqueous coating composition and paint |
| NZ314294A (en) * | 1996-03-06 | 1998-07-28 | Rohm & Haas | Fast drying coating composition having early water resistance comprising a latex derivative, use thereof |
| US6028155A (en) * | 1997-05-21 | 2000-02-22 | Eastman Chemical Company | Surfactant-containing acetoacetoxy-functional and enamine-functional polymers |
| EP0902800B1 (en) | 1996-05-28 | 2002-09-11 | Eastman Chemical Company | Surfactant-containing acetoacetoxy-functional and enamine-functional polymers |
| US5998543A (en) * | 1996-05-28 | 1999-12-07 | Eastman Chemical Company | Stable amino-containing polymer latex blends |
| US6417267B1 (en) | 1996-05-28 | 2002-07-09 | Eastman Chemical Company | Adhesive compositions containing stable amino-containing polymer latex blends |
| US5891950A (en) * | 1996-05-28 | 1999-04-06 | Eastman Chemical Company | Use of stable amino-functional latexes in water-based inks |
| US5744239A (en) * | 1996-09-27 | 1998-04-28 | Minnesota Mining And Manufacturing Company | Addition of antimicrobial agents to pavement marking materials |
| US5962556A (en) * | 1996-10-22 | 1999-10-05 | Eastman Chemical Company | Functional latexes resistant to hydrolysis |
| US6413011B1 (en) * | 1997-02-26 | 2002-07-02 | Rohm And Haas Company | Method for producing fast-drying multi-component waterborne coating compositions |
| AU738464B2 (en) * | 1997-04-22 | 2001-09-20 | Rohm And Haas Company | Wear-resistant traffic marking composition |
| ES2178215T3 (es) * | 1997-05-21 | 2002-12-16 | Eastman Chem Co | Procedimiento para preparar mezclas de latex reactivo que son quimica y fisicamente estables en la formacion de peliculas. |
| US6090882A (en) * | 1997-05-30 | 2000-07-18 | S. C. Johnson Commercial Markets, Inc. | Crosslinkable surface coatings and process of preparation |
| BR9810030A (pt) * | 1997-06-13 | 2000-09-12 | Eastman Chem Co | Composições de balizamento de tráfego adesivo de fusão quente, amarelas. |
| AU7195598A (en) | 1997-07-03 | 1999-01-14 | Rohm And Haas Company | Coating method and coating composition used therein |
| US6649679B1 (en) | 1997-09-18 | 2003-11-18 | Eastman Chemical Company | Stable waterborne polymer compositions containing poly(alkylenimines) |
| CA2330954A1 (en) | 1998-05-01 | 1999-11-11 | Mbt Holding Ag | Integrated retroreflective marking materials |
| DE69941188D1 (de) | 1998-05-19 | 2009-09-10 | Du Pont | Verwendung einer Vernetzerkomponente enthaltend ein Polyamin und/oder ein Polyketimin |
| DE19839199A1 (de) | 1998-08-28 | 2000-03-02 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
| DE19840586A1 (de) | 1998-09-05 | 2000-03-09 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
| DE19911170A1 (de) | 1999-03-12 | 2000-09-14 | Basf Ag | Verfahren zum Herstellen von W/O-Emulsionen |
| US6337106B1 (en) | 1999-06-01 | 2002-01-08 | Rohm And Haas | Method of producing a two-pack fast-setting waterborne paint composition and the paint composition therefrom |
| US6107367A (en) * | 1999-06-16 | 2000-08-22 | Jackson Products, Inc. | Traffic stripe composition |
| US6475556B1 (en) | 1999-11-25 | 2002-11-05 | Rohm And Haas Company | Method for producing fast drying multi-component waterborne coating compositions |
| AU775470B2 (en) | 2000-03-03 | 2004-08-05 | Rohm And Haas Company | Removable coating composition and preparative method |
| EP1170340A1 (en) * | 2000-07-05 | 2002-01-09 | Rohm And Haas Company | Wear-resistant coating composition and method for producing a coating |
| US6521715B1 (en) | 2000-08-22 | 2003-02-18 | E. I. Du Pont De Nemours And Company | Graft copolymer pigment dispersants |
| EP1352931B1 (en) * | 2002-04-10 | 2008-03-19 | Rohm And Haas Company | Method of applying traffic marking onto an oily road surface and traffic paints formulated therefor |
| US20030224184A1 (en) | 2002-05-07 | 2003-12-04 | Hermes Ann Robertson | Method of producing wear resistant traffic markings |
| DE10317434A1 (de) | 2003-04-15 | 2004-10-28 | Basf Ag | Verfahren zur Reduzierung der Restmonomerenmenge in wässrigen Polymerdispersionen |
| DE10335958A1 (de) | 2003-08-04 | 2005-02-24 | Basf Ag | Verfahren zur Herstellung wässriger Polymerisatdispersionen |
| US9732481B2 (en) * | 2004-04-02 | 2017-08-15 | Flint Trading, Inc. | Preformed thermoplastic pavement marking and method utilizing large aggregate for improved long term skid resistance and reduced tire tracking |
| US7470751B2 (en) * | 2004-09-21 | 2008-12-30 | Basf Corporation | Stabilized water-borne polymer compositions for use as water-based coatings |
| US7947760B2 (en) | 2004-09-21 | 2011-05-24 | Basf Corporation | Emulsion compositions for use in printing inks |
| JP2007092030A (ja) * | 2005-08-05 | 2007-04-12 | Rohm & Haas Electronic Materials Llc | 改善された不透明なコーティング |
| US7538151B2 (en) * | 2005-08-22 | 2009-05-26 | Rohm And Haas Company | Coating compositions and methods of coating substrates |
| WO2007059516A1 (en) | 2005-11-15 | 2007-05-24 | Valspar Sourcing, Inc. | Crush resistant latex topcoat composition for fiber cement substrates |
| CN101374787B (zh) * | 2006-01-31 | 2013-12-11 | 威士伯采购公司 | 涂布水泥纤维板制品的方法 |
| US9783622B2 (en) | 2006-01-31 | 2017-10-10 | Axalta Coating Systems Ip Co., Llc | Coating system for cement composite articles |
| CA2636435C (en) | 2006-01-31 | 2013-10-22 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| EP1979426A1 (en) * | 2006-01-31 | 2008-10-15 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| EP2361955B1 (en) | 2006-05-19 | 2014-12-17 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| DE602007012700D1 (de) | 2006-06-02 | 2011-04-07 | Valspar Sourcing Inc | Wässrige hochleistungsbeschichtungszusammensetzungen |
| US7812090B2 (en) * | 2006-06-02 | 2010-10-12 | Valspar Sourcing, Inc. | High performance aqueous coating compositions |
| ES2716987T3 (es) | 2006-07-07 | 2019-06-18 | Swimc Llc | Sistemas de recubrimiento para artículos composite de cemento |
| AU2008200079B2 (en) | 2007-01-16 | 2012-03-29 | Rohm And Haas Company | Fast-drying aqueous compositions with hollow particle binders and traffic paints made therewith |
| MX2008002220A (es) | 2007-02-16 | 2009-02-25 | Valspar Sourcing Inc | Tratamiento para articulos compuestos de cemento. |
| AU2008255216B2 (en) | 2008-01-07 | 2013-03-28 | Rohm And Haas Company | Fast dry, shelf stable-aqueous coating composition comprising a phosphorus acid polymer |
| US8389061B2 (en) * | 2008-02-01 | 2013-03-05 | Arkema Inc. | Aqueous emulsion polymer for scrub resistance and wet adhesion |
| MX2011001736A (es) | 2008-08-15 | 2011-05-10 | Valspar Sourcing Inc | Composicion de recubrimiento de sustrato cementoso de auto-grabado. |
| AU2009316285A1 (en) | 2008-11-24 | 2010-05-27 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| DE102009002888A1 (de) | 2009-05-07 | 2010-11-11 | Evonik Röhm Gmbh | Beschichtungsmittel, Verfahren zur Herstellung einer Beschichtung und beschichteter Gegenstand |
| WO2011058163A1 (en) | 2009-11-16 | 2011-05-19 | Dsm Ip Assets B.V. | Acrylic polymer |
| EP2333022B1 (en) * | 2009-12-09 | 2012-06-27 | Rohm and Haas Company | High PVC fast-drying aqueous binder compositions with small particle binders and traffic markings made therewith |
| DE102010002123A1 (de) * | 2010-01-26 | 2011-07-28 | Evonik Röhm GmbH, 64293 | Formulierungen zur Herstellung von Fahrbahnmarkierungen mit Haftung auf trockenem und feuchtem Boden |
| BR112013012584A2 (pt) | 2010-12-02 | 2016-08-09 | Dsm Ip Assets Bv | polímero acrílico |
| US8809447B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Acetoacetate-functional monomers and their uses in coating compositions |
| US9029451B2 (en) | 2010-12-15 | 2015-05-12 | Eastman Chemical Company | Waterborne coating compositions that include 2,2,4-trimethyl-3-oxopentanoate esters as reactive coalescents |
| US8809446B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Substituted 3-oxopentanoates and their uses in coating compositions |
| JP5837531B2 (ja) * | 2012-04-27 | 2015-12-24 | 菊水化学工業株式会社 | 水性塗料の塗布方法、水性塗料セット及び水性塗料用硬化促進剤 |
| EP2945994B1 (en) | 2013-01-18 | 2018-07-11 | Basf Se | Acrylic dispersion-based coating compositions |
| WO2014161817A1 (de) | 2013-04-03 | 2014-10-09 | Basf Se | Verfahren zur reduzierung der restmonomerenmenge in einer wässrigen polymerisatdispersion |
| EP2965785A1 (en) | 2014-07-11 | 2016-01-13 | DSM IP Assets B.V. | Novel use |
| AU2016202331B2 (en) | 2015-04-30 | 2020-08-13 | Rohm And Haas Company | Durable aqueous compositions for use in making traffic markings having good dirt pickup resistance and traffic markings made therewith |
| US10829591B2 (en) * | 2015-06-23 | 2020-11-10 | Arkema Inc. | Latex products having polymers and polymer adducts as quick-setting additives |
| MX2017016917A (es) | 2015-06-23 | 2018-08-23 | Arkema Inc | Polimeros solubles en agua y aductos polimericos junto con soluciones acuosas de los mismos. |
| US10584207B2 (en) | 2015-06-23 | 2020-03-10 | Arkema Inc. | Quick-setting coating compositions with low pH stability and water resistance |
| CN105295674B (zh) * | 2015-11-14 | 2017-12-29 | 苏州大乘环保新材有限公司 | 水性道路标线漆及其制备方法 |
| BR112018070049B1 (pt) * | 2016-03-31 | 2022-12-06 | Rohm And Haas Company | Composição aquosa, e, método para produzir uma marcação de trânsito ou outro substrato revestido |
| CN110291164A (zh) * | 2016-11-22 | 2019-09-27 | 宣伟投资管理有限公司 | 低气味水基涂料组合物 |
| CA3068453A1 (en) | 2017-06-28 | 2019-01-03 | Rohm And Haas Company | Storage stable quicksetting coating system that is free of volatile-base |
| AU2017239540A1 (en) | 2017-08-09 | 2019-02-28 | Pidilite Industries Limited | Organic-inorganic hybrid polymer latex for high durable traffic marking paint |
| EP3728354A1 (en) | 2017-12-22 | 2020-10-28 | DSM IP Assets B.V. | Adhesive compositions and their use in 3d printing |
| BR112021005765B1 (pt) | 2018-10-10 | 2023-12-12 | Dow Global Technologies Llc | Composição à base de água e revestimento, selante ou acabamento de alvenaria |
| EP3778787A1 (en) | 2019-08-12 | 2021-02-17 | M. Swarovski Gesellschaft m.b.H. | Paint composition |
| EP4526269A4 (en) | 2022-05-20 | 2026-04-08 | Rohm & Haas | METHOD FOR APPLYING A COATING COMPOSITION TO A SUBSTRATE |
| WO2024233443A1 (en) | 2023-05-09 | 2024-11-14 | Rohm And Haas Company | Bimodal binder compositions, processes of making bimodal binder compositions, and fast-drying aqueous compositions comprising a bimodal binder composition |
| AU2024269142A1 (en) | 2023-05-09 | 2025-12-11 | Rohm And Haas Company | Bimodal binder compositions, processes of making bimodal binder compositions, and fast-drying aqueous compositions comprising a bimodal binder composition |
| EP4709800A1 (en) | 2023-05-09 | 2026-03-18 | Rohm and Haas Company | Bimodal binder compositions, processes of making bimodal binder compositions, and fast-drying aqueous compositions comprising a bimodal binder compostion |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4812493A (en) * | 1987-04-10 | 1989-03-14 | Adhesive Coatings Co. | Dual cure rate water-based coating compositions |
| CA2020629C (en) * | 1989-07-21 | 2000-02-01 | Frank Landy | Shelf stable fast-cure aqueous coating |
| SE468856B (sv) * | 1990-07-11 | 1993-03-29 | Ultralux Ab | Fluorescerande vaegmarkering |
| DE69124354T3 (de) * | 1990-12-21 | 2003-04-24 | Rohm And Haas Co., Philadelphia | Lufthärtende Polymerzusammensetzung |
| EP0525977A1 (en) * | 1991-06-28 | 1993-02-03 | Morton International, Inc. | Fast dry waterborne traffic marking paint |
| JP3300458B2 (ja) * | 1993-03-18 | 2002-07-08 | アトミクス株式会社 | 水性の路面標示用組成物 |
| GB9305548D0 (en) * | 1993-03-18 | 1993-05-05 | Zeneca Ltd | Crosslinkable coating compositions |
| ZA947530B (en) * | 1993-09-29 | 1995-05-29 | Ici Australia Operations | Water-borne crosslinkable aminoalkyl-alkoxysilane coatings |
| US5534310A (en) * | 1994-08-17 | 1996-07-09 | Rohm And Haas Company | Method of improving adhesive of durable coatings on weathered substrates |
| CA2210807A1 (en) * | 1995-01-18 | 1996-07-25 | The Dow Chemical Company | Fast hardening aqueous coating composition and paint |
-
1996
- 1996-07-26 US US08/687,851 patent/US5672379A/en not_active Expired - Lifetime
- 1996-08-19 TW TW085110080A patent/TW353110B/zh not_active IP Right Cessation
- 1996-09-09 DE DE69625146T patent/DE69625146T2/de not_active Expired - Lifetime
- 1996-09-09 EP EP96306522A patent/EP0764699B1/en not_active Expired - Lifetime
- 1996-09-09 AU AU65519/96A patent/AU701280B2/en not_active Expired
- 1996-09-10 NZ NZ299341A patent/NZ299341A/xx unknown
- 1996-09-10 SG SG1996010581A patent/SG68592A1/en unknown
- 1996-09-16 CA CA002185637A patent/CA2185637A1/en not_active Abandoned
- 1996-09-19 MX MX9604188A patent/MX9604188A/es unknown
- 1996-09-20 CN CN96112837A patent/CN1070900C/zh not_active Expired - Lifetime
- 1996-09-20 JP JP27149496A patent/JP4107691B2/ja not_active Expired - Fee Related
-
1997
- 1997-05-06 US US08/851,994 patent/US5820993A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117355573A (zh) * | 2021-06-21 | 2024-01-05 | 罗门哈斯公司 | 成膜性和非成膜性聚合物颗粒的水性分散体 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0764699A3 (en) | 1997-04-02 |
| DE69625146D1 (de) | 2003-01-16 |
| MX9604188A (es) | 1998-04-30 |
| AU701280B2 (en) | 1999-01-21 |
| AU6551996A (en) | 1997-03-27 |
| US5820993A (en) | 1998-10-13 |
| JP4107691B2 (ja) | 2008-06-25 |
| EP0764699B1 (en) | 2002-12-04 |
| US5672379A (en) | 1997-09-30 |
| TW353110B (en) | 1999-02-21 |
| CN1147003A (zh) | 1997-04-09 |
| NZ299341A (en) | 1999-02-25 |
| JPH09124974A (ja) | 1997-05-13 |
| DE69625146T2 (de) | 2003-07-24 |
| CN1070900C (zh) | 2001-09-12 |
| EP0764699A2 (en) | 1997-03-26 |
| SG68592A1 (en) | 1999-11-16 |
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Effective date: 20010917 |