USRE31936E - Dispersing paint pigments - Google Patents
Dispersing paint pigments Download PDFInfo
- Publication number
- USRE31936E USRE31936E US06/536,821 US53682183A USRE31936E US RE31936 E USRE31936 E US RE31936E US 53682183 A US53682183 A US 53682183A US RE31936 E USRE31936 E US RE31936E
- Authority
- US
- United States
- Prior art keywords
- methacrylate
- copolymer
- acrylate
- component
- iadd
- 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.)
- Expired - Lifetime
Links
- 239000000049 pigment Substances 0.000 title claims abstract description 54
- 239000003973 paint Substances 0.000 title claims abstract description 52
- 229920001577 copolymer Polymers 0.000 claims abstract description 74
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000002270 dispersing agent Substances 0.000 claims abstract description 40
- -1 hydroxyalkyl ester Chemical class 0.000 claims abstract description 36
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 33
- 150000003839 salts Chemical class 0.000 claims abstract description 32
- 229920000642 polymer Polymers 0.000 claims abstract description 18
- 229920000126 latex Polymers 0.000 claims abstract description 14
- 239000000839 emulsion Substances 0.000 claims abstract description 13
- 239000004816 latex Substances 0.000 claims abstract description 13
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 42
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 34
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 29
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 150000002148 esters Chemical group 0.000 claims description 22
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims description 18
- 239000000178 monomer Substances 0.000 claims description 18
- 159000000000 sodium salts Chemical class 0.000 claims description 17
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims description 15
- 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 15
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 15
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 14
- 239000006185 dispersion Substances 0.000 claims description 14
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 claims description 12
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 12
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 claims description 12
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- 150000001340 alkali metals Chemical class 0.000 claims description 9
- 150000001408 amides Chemical class 0.000 claims description 9
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 9
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 7
- 229940051250 hexylene glycol Drugs 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 5
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 5
- LMAUULKNZLEMGN-UHFFFAOYSA-N 1-ethyl-3,5-dimethylbenzene Chemical compound CCC1=CC(C)=CC(C)=C1 LMAUULKNZLEMGN-UHFFFAOYSA-N 0.000 claims description 4
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 claims description 4
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical group CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 3
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 19
- 150000003863 ammonium salts Chemical class 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 2
- 238000010348 incorporation Methods 0.000 claims 2
- MUZDXNQOSGWMJJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=C)C(O)=O MUZDXNQOSGWMJJ-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 14
- 239000007787 solid Substances 0.000 description 13
- 102100026735 Coagulation factor VIII Human genes 0.000 description 10
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 5
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 4
- 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 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 3
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-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
- 239000004908 Emulsion polymer Substances 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000019241 carbon black Nutrition 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 1
- XFKFBBVGUXNVOU-UHFFFAOYSA-N (4,5-dihydroxy-2-methylpent-2-en-3-yl) 2-methylprop-2-enoate Chemical compound OCC(O)C(=C(C)C)OC(=O)C(C)=C XFKFBBVGUXNVOU-UHFFFAOYSA-N 0.000 description 1
- ARFDIYMUJAUTDK-UHFFFAOYSA-N 1-hydroxypentyl 2-methylpropanoate Chemical compound CCCCC(O)OC(=O)C(C)C ARFDIYMUJAUTDK-UHFFFAOYSA-N 0.000 description 1
- IUXYVKZUDNLISR-UHFFFAOYSA-N 2-(tert-butylamino)ethanol Chemical compound CC(C)(C)NCCO IUXYVKZUDNLISR-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241001561902 Chaetodon citrinellus Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- VAPILSUCBNPFBS-UHFFFAOYSA-L disodium 2-oxido-5-[[4-[(4-sulfophenyl)diazenyl]phenyl]diazenyl]benzoate Chemical compound [Na+].[Na+].Oc1ccc(cc1C([O-])=O)N=Nc1ccc(cc1)N=Nc1ccc(cc1)S([O-])(=O)=O VAPILSUCBNPFBS-UHFFFAOYSA-L 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011953 free-radical catalyst Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 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
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000001038 titanium pigment Substances 0.000 description 1
- 229940086542 triethylamine Drugs 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-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
- 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
- C09D133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
-
- 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
- C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
Definitions
- This invention concerns the improvement of water-based, emulsion coating compositions containing a film-forming latex polymer and dispersed pigment, and especially of those compositions containing alkylene glycols and intended to yield moderate to high specular gloss, wherein is incorporated, as pigment dispersant, a water-soluble salt of a relativelly low molecular weight copolymer of certain polar alkyl acrylates or methacrylates and acrylic or methacrylic acid which is compatible with and improves the properties of said aqueous and glycol-containing, pigmented paints.
- the invention also concerns improved fluid pigment pastes of high solids and low water content containing salt of said copolymer.
- U.S. Pat. No. 3,840,487 describes dispersing agents which are the salts of the copolymers of 40-95 mole percent acrylic or methacrylic acid and 5 to 60 mole percent of non-functional alkyl acrylate ester. Although such disclosed polyacrylate type compositions are good dispersing agents, we have found they confer greater foaming tendency, have poor stability, and confer generally poorer adhesion and less gloss to latex paint formulations than the copolymers used herein.
- U.S. Pat. Nos. 3,645,099 and 3,859,260 disclose water-soluble oligomers of the formulas H-(hydroxyethyl acrylate) 10 -(acrylic acid) 1 -SO 3 Na and H-(hydroxypropyl acrylate) 5 -(acrylic acid) 15 -SO 3 An which are described as useful as conductive agents and surface active agents. There is no suggestion that such sulfonate (sulfamate) salts of said oligomers could be used as pigment dispersants in paint formulations.
- the pigment dispersant embodied in this invention is the water-soluble, alkali metal (e.g., sodium, potassium), ammonium, or amine (e.g., triethyl amine, dimethylaminoethanol, 2-amino-2-methyl-1-propanol, ethyl amine, diethyl amine, butyl amine, ethanol amine, N-methyl ethanol amine, and the like) salt of a copolymer consisting essentially of polymerized units of .[.(A) 45 to 90 weight percent, preferably 55 to 80%, and more preferably 60-75%, of at least one hydroxyalkylester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms, preferably two to three, (representative esters include 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl
- esters include 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 2,3-dihydroxypropyl acrylate, and the like); and
- the copolymer may optionally contain minor amounts, i.e., up to about 30% of polymerized units of other monomers which, in such limited amounts, do not .[.effect.]. .Iadd.affect .Iaddend.the solubility of the copolymer.
- Such comonomers include methyl acrylate, ethyl acrylate, n-butyl acrylate, sec-butyl acrylate, isobutyl acrylate, t-butyl acrylate, the corresponding methacrylate analogs, acrylamide, acrylonitrile, and diacetone acrylamide.
- the number average molecular weight of the copolymer dispersant embodied herein is in the range of about 500 to about 15,000, preferably from about 1,000 to about 10,000, determined by gel permeation chromatography.
- the copolymer dispersants are prepared by solution polymerization techniques in aqueous media which optionally for economy and convenience may contain the desired alkylene glycol diluent.
- the appropriate monomeric mixture is generally reacted under oxygen-free conditions at temperatures within the range of about 30° to 150° C. in the presence of such free radical initiators as t-butyl peroxypivalate, t-butyl peracetate, ammonium persulfate, t-butyl hydroperoxide, cumene hydroperoxide, and like free radical catalysts including free radial redox polymerization initiators.
- Catalyst concentrations of about 1 to 15% by weight of the monomers are useful to obtain the low molecular weight polymers desired.
- a method for improving the properties and performance of an aqueous emulsion (latex) paint comprising a mixture of a film-forming latex polymer and a pigment dispersion, from about 0.1 to about 5%, based on weight of the pigment, preferably 0.1 to 2%, of the aforedescribed copolymer salt is incorporated.
- An additional embodiment of the invention involves such an aqueous emulsion paint formulation modified for higher gloss by the addition thereto of from about 0.1 to about 2 pounds, preferably 0.5 to 1.3 lbs., of alkylene glycol per gallon of paint.
- the alkylene glycol for example, ethylene glycool, propylene glycol, which is preferred, and hexylene glycol, functions to slow the drying rate of the paint, increasing the wet-edge time, and to improve leveling, as well as generally causing the development of higher glass than with an all aqueous system.
- Suitable latexes for paints are aqueous addition polymer dispersions, generally obtained most conveniently by direct emulsion polymerization.
- the most important of these dispersions used in making water-based paints are polymers including homopolymers and copolymers of: (1) vinyl esters of an aliphatic acid having 1 to 18 carbon atoms, especially vinyl acetate; (2) acrylic acid esters and methacrylic acid esters of an alcohol having 1 to 18 carbon atoms, especially methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylte, ethyl methacrylate and butyl methacrylate; and (3) mono- and di-ethylenically unsaturated hydrocarbons, such as ethylene, isobutylene, styrene, and alipatic dienes, such as butadiene, isoprene, and chloroprene.
- Homopolymers of ethylene, isobutylene, and styrene, and copolymers of one or more of these hydrocarbons with one or more esters, nitriles or amides of acylic acid or of methacrylic acid or with vinyl esters, such as vinyl acetate and vinyl chloride, or with vinylidene chloride are also used.
- the diene polymers are generally used in aqueous base paints in the form of copolymers with one or more monomers following: styrene, vinyltoluene, acrylonitrile, methacrylonitrile, and the abovementioned esters of acrylic acid or methacrylonitrile, and the abovementioned esters of acrylic acid or methacrylic acid. It is also quite common to include a small amount, such as 1/2 to 2.5% or more, of an acid monomer in the monomer mixture used for making the copolymers for all three general types mentioned above by emulsion polymerzation. Acids used include acrylic, methacrylic, itaconic, aconitic, citraconic, crotonic, maleic, fumaric, the dimer of acrylic acid, and so on.
- aqueous dispersions as the emulsion polymer in the paint may be made using one or more emulsifiers of anionic, cationic, or non-ionic type. Mixtures of two or more emulsifiers rgardless of type may be used, except that it is generally undesirable to mix a cationic with an anionic type in any appreciable amounts since they tend to neutralize each other.
- the amount of emulsifier may range from about 0.1 to 6% by weight or sometimes even more, based on the weight of the total monomer charge.
- emulsifiers When using a persulfate type of initiator, the addition of emulsifiers is often unnecessary and this omission or the use of only a small amount, e.g., less than about 0.5%, of emulsifier, may sometimes be desirable from the cost standpoint (elimination of expensive emulsifier), and less sensitivity of the dried coating or impregnation to moisture, and hence less liability of the coated substrate to be affected by moisture, which, for instance, would produce coatings less liable to swelling or softening, particularly when subjected to humid atmospheres.
- the average particle size or diameter of these dispersed polymers may be from about 0.03 to 3 microns or even larger.
- the particle size is the "weight average diameter.” This number, expressed in microns, is determined using the ultra-centrifuge. A description of the method can be found in the Journal of Colloid Science 15, pp. 563-572, 1960 (J. Brodnyan). In general, the molecular weights of these emulsion polymers are high, e.g., from about 100,000 to 10 million viscosity average, most commonly above 500,000.
- a gallon of emulsion paint is comprised of about 0.5 to 3 lbs. of film-forming resin and about 0.2 to about 5 lbs. of finely-divided pigment.
- Typical pigments are titanium dioxide and other titanium pigments, white lead, zinc, oxide, zinc sulfide, barium sulfate, calcium carbonate, lithopone, silica, talc, mica, clays, iron oxide, carbon black, cadmium sulfide, toluidene red, chrome orange, chrome yellow, chrome green, and others known in the artm.
- Tyical latices of film-forming resins are those of the alkyl acrylates and methacrylates, vinyl acetate, styrene-butadiene, and others known in the art. Minor amounts of other coatings additives may be included in the paint formulations, for example, antifoams, mildewcides, thickeners, wetting agents, bacteriostats, etc.
- Another aspect of the invention is the provision of dispersions of pigments as fluid pastes of high solids content and low aqueous media content (said aqueous media comprising water or water and a minor or major proportion of alkylene glycol as aforementioned) containing in admixture a relatively minor amount of the described water-soluble salt of the copolymer of ethylenically unsaturated acid and the hydroxyalkyl ester thereof as dispersant.
- the amount of the salt of the copolymer effecting dispersion of solids and fluidity of the pigment paste will usually not be over about three percent of the weight of pigment and may be as low as about 0.05%.
- aqueous solution of copolymer in salt form Concentrations of 5 to 40% may be used, although those of 10 to 20% are usually preferred.
- Pigment, water (including an alkylene glycol), and solutions are mixed.
- the paste or suspension may be ground in a mill--a pebble mill, roll mill, colloid mill, or high speed stone mill, or in some instances a high shear mixer being suitable.
- Sufficient copolymer is used to ensure good dispersion and fluidity of the paste. The optimum amount of copolymer will depend upon the specific pigmement or pigments and upon the state of subdivision thereof. In general, the finer the particle size the more dispersant should be used.
- Concentrated pastes can be extended to give dilute pastes, when the latter are needed.
- the pigment pastes are a suitable and convenient composition for addition to aqueous resin latexes or dispersions, as previously discussed, to form emulsion paints.
- fluid pastes of certain pigments have diverse uses, for example, such high solids content slurries of calcium hydroxide are useful for coatings as white-wash, field markings, or the like, or as concentrated alkaline reagents in chemical manufacturing; dispersions of carbon blacks in aqueous media are useful in the fields of paper, cement, water-base paints, coating compositions, inks, rayons, and rubber.
- the pigments may be present in the foregoing pastes in an amount up to 85% by weight of the paste.
- MAA methacrylic acid
- HMPA 2-hydroxypropyl methacrylate
- a monomer mixture of 143 g. HEMA and 94.6 g. glacial MAA is added simultaneously over a one hour period with the addition of a solution of 18.8 g. "Lupersol 11" (57% t-butyl peroxypivalate) in 94 g. isopropanol while maintaining the reactor contents at reflux (84° C.). Reflux is maintained for another hour.
- the dissolved copolymer is composed of HEMA/MAA in a 60/40 weight ratio.
- a reaction flask as described above is charged with 300 g. propylene glycol which is heated to 150° C. under nitrogen blanket.
- a solution of 210 g. HEMA, 90 g. MMA, 3 g. mercaptoethanol and 12 g. "Lupersol 70" (75% t-butyl peracetate) is added over a five hour period while maintaining temperature at 150° C. Addition of 1.2 g. more of "Lupersol 70" without exotherm indicates completion of reaction; however, heating is continued for 30-45 minutes.
- a five-liter flask equipped as those described above is charged with 1955 g. water and 567.3 g. propylene glycol and the solution heated to 90° C. while sparging with nitrogen. 45% of a catalyst solution of 62.5 g. ammonium persulfate in 312.5 g. water is added, and then the remainder of the catalyst solution and 480.75 g. MAA and 1121.75 g. HEMA are added simultaneously over a 1.5 hours period. The reaction mixture is held at 92°-95° C. for an additional hour. The viscosity of the mixture is 82.5 cps. (LV, #2, 60 rpm).
- the mixture is cooled and 430 g. of 50% aqueous NaOh are added gradually to give a pH of 9.6.
- the propylene glycol content of the solution is 11.2%, dissolved solids content is 42%, viscosity 360 cps. (LV #2, 30 rpm); when diluted to 25% solids, viscosity is 23 centipoise.
- the dissolved copolymer is composed HEMA/MAA in a 70/30 weight ratio.
- the paint formulations are evaluated for the critical properties of specular gloss, viscosity at high and low shear rate, and stability thereof when subjected to elevated temperature and to freeze-thaw cycling in accordance with the following procedures.
- dispersant samples are diluted to 5 weight percent solids with water and shaken vigorously in jars. With the exception of the control dispersant used in Formulation b, all of the materials confer little or no foaming tendency.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
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- Paints Or Removers (AREA)
Abstract
An improved glossy, aqueous emulsion paint comprised of a mixture of a film-forming latex polymer and dispersed pigment is prepared by incorporating therein, as pigment dispersant, a water-soluble salt of a low molecular weight copolymer of hydroxyalkyl ester of acrylic or methacrylic acid and acrylic or methacrylic acid.
Description
This application is a continuation, of application Ser. No. 006,132, filed Jan. 24, 1979. .Iaddend.
This invention concerns the improvement of water-based, emulsion coating compositions containing a film-forming latex polymer and dispersed pigment, and especially of those compositions containing alkylene glycols and intended to yield moderate to high specular gloss, wherein is incorporated, as pigment dispersant, a water-soluble salt of a relativelly low molecular weight copolymer of certain polar alkyl acrylates or methacrylates and acrylic or methacrylic acid which is compatible with and improves the properties of said aqueous and glycol-containing, pigmented paints. The invention also concerns improved fluid pigment pastes of high solids and low water content containing salt of said copolymer.
The use of low molecular weight polyelectrolytes as dispersing agents for pigments in water-based coatings is well known. U.S. Pat. No. 2,930,775 discloses that salts of copolymers of olefins and maleic anhydride are operable therefor. However, while these dispersants are excellent for many uses, formulations containing these dispersants often exhibit a tendency to foam, sometimes product coatings having inadequate adhesion, and may exhibit poor stability, especially in the presence of divalent cations deriving either from so-called reactive pigments containing zine, barium, lead, etc., or from paint formulation additives containing such cations.
British Pat. No. 998,380 (and its counter part, U.S. Pat. No. 3,223,751) teach that anionic copolymers of three moles of acrylamide and one mole of itaconic acid, or the salts thereof, are pigment dispersing agents. U.S. Pat. No. 3,320,275 deals with interpolymers of 5-45% acrylamide, at least 20% of an acrylic ester, 2-25% of a hydroxyalkylester of an unsaturated acid, and up to 15% of a carboxylic acid monomer which heat cure to form hard, flexible, solvent resistant coatings; however, the use of these resins in aqueous system formulations is not suggested or contemplated.
U.S. Pat. No. 3,840,487 describes dispersing agents which are the salts of the copolymers of 40-95 mole percent acrylic or methacrylic acid and 5 to 60 mole percent of non-functional alkyl acrylate ester. Although such disclosed polyacrylate type compositions are good dispersing agents, we have found they confer greater foaming tendency, have poor stability, and confer generally poorer adhesion and less gloss to latex paint formulations than the copolymers used herein. Such differences on a balance between a hydrophobic comonomer and (meth)acrylic acid to achieve solubility of the copolymer dispersant in alkylene glycols, whereas we rely on hydrophilic and hydrogen-bondable, yet nonionic, comonomers to promote solubility.
U.S. Pat. Nos. 3,645,099 and 3,859,260 disclose water-soluble oligomers of the formulas H-(hydroxyethyl acrylate)10 -(acrylic acid)1 -SO3 Na and H-(hydroxypropyl acrylate)5 -(acrylic acid)15 -SO3 An which are described as useful as conductive agents and surface active agents. There is no suggestion that such sulfonate (sulfamate) salts of said oligomers could be used as pigment dispersants in paint formulations.
The pigment dispersant embodied in this invention is the water-soluble, alkali metal (e.g., sodium, potassium), ammonium, or amine (e.g., triethyl amine, dimethylaminoethanol, 2-amino-2-methyl-1-propanol, ethyl amine, diethyl amine, butyl amine, ethanol amine, N-methyl ethanol amine, and the like) salt of a copolymer consisting essentially of polymerized units of .[.(A) 45 to 90 weight percent, preferably 55 to 80%, and more preferably 60-75%, of at least one hydroxyalkylester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms, preferably two to three, (representative esters include 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 2,3-dihydroxypropyl acrylate, and the like); and (B) 10 to 55 weight percent, preferably 20 to 45%, and more preferably 25-40%, of acrylic acid or methacrylic acid..].
(.Iadd.A) 30 to 90 weight percent, preferably 45 to 90% more preferably 55 to 80%, and still more preferably 60-75%, of at least one hydroxyalkylester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms, preferably two to three, (representative esters include 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 2,3-dihydroxypropyl acrylate, and the like); and
(B) 10 to 70 weight percent; preferably 10 to 55%, more preferably 20 to 45%, and still more preferably 25-40%, of acrylic acid, methacrylic acid, itaconic acid, or the half ester or half amide of itaconic acid, preferably methacrylic acid. .Iaddend.
Of course, mixtures of the various monomers can be used.
The copolymer may optionally contain minor amounts, i.e., up to about 30% of polymerized units of other monomers which, in such limited amounts, do not .[.effect.]. .Iadd.affect .Iaddend.the solubility of the copolymer. Such comonomers include methyl acrylate, ethyl acrylate, n-butyl acrylate, sec-butyl acrylate, isobutyl acrylate, t-butyl acrylate, the corresponding methacrylate analogs, acrylamide, acrylonitrile, and diacetone acrylamide.
The number average molecular weight of the copolymer dispersant embodied herein is in the range of about 500 to about 15,000, preferably from about 1,000 to about 10,000, determined by gel permeation chromatography.
The copolymer dispersants are prepared by solution polymerization techniques in aqueous media which optionally for economy and convenience may contain the desired alkylene glycol diluent. The appropriate monomeric mixture is generally reacted under oxygen-free conditions at temperatures within the range of about 30° to 150° C. in the presence of such free radical initiators as t-butyl peroxypivalate, t-butyl peracetate, ammonium persulfate, t-butyl hydroperoxide, cumene hydroperoxide, and like free radical catalysts including free radial redox polymerization initiators. Catalyst concentrations of about 1 to 15% by weight of the monomers are useful to obtain the low molecular weight polymers desired. Sufficient alkali metal hydroxide, ammonium hydroxide, or watersoluble amine, preferably a slight excess, is added during polymerization or subsequently to neutralize free acid groups on the copolymer, thus converting the dispersant to the operable salt. As is well known, catalyst fragments such as derived from a persulfate may appear as part of the polymer. In accordance with this invention, a method for improving the properties and performance of an aqueous emulsion (latex) paint is provided, wherein said paint, comprising a mixture of a film-forming latex polymer and a pigment dispersion, from about 0.1 to about 5%, based on weight of the pigment, preferably 0.1 to 2%, of the aforedescribed copolymer salt is incorporated. An additional embodiment of the invention involves such an aqueous emulsion paint formulation modified for higher gloss by the addition thereto of from about 0.1 to about 2 pounds, preferably 0.5 to 1.3 lbs., of alkylene glycol per gallon of paint. The alkylene glycol, for example, ethylene glycool, propylene glycol, which is preferred, and hexylene glycol, functions to slow the drying rate of the paint, increasing the wet-edge time, and to improve leveling, as well as generally causing the development of higher glass than with an all aqueous system.
Suitable latexes for paints are aqueous addition polymer dispersions, generally obtained most conveniently by direct emulsion polymerization. The most important of these dispersions used in making water-based paints are polymers including homopolymers and copolymers of: (1) vinyl esters of an aliphatic acid having 1 to 18 carbon atoms, especially vinyl acetate; (2) acrylic acid esters and methacrylic acid esters of an alcohol having 1 to 18 carbon atoms, especially methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylte, ethyl methacrylate and butyl methacrylate; and (3) mono- and di-ethylenically unsaturated hydrocarbons, such as ethylene, isobutylene, styrene, and alipatic dienes, such as butadiene, isoprene, and chloroprene.
Poly(vinyl acetate) and copolymers of vinyl acetate with one or more of the following monomers; vinyl chloride, vinylidene chloride, styrene, vinyltoluene, acrylonitrile, methacrylonitrile, one or two of the acrylic and methacrylic acid esters mentioned above are well known as the film-forming component of aqueous base paints. Similarly copolymers of one or more of the a crylic or methacrylic acid esters mentioned above with one or more of the following monomers: vinyl acetate, vinyl chloride, vinylidene chloride, styrene, vinyltoluene, acrylonitrile, and methacrylonitrile are also more or less conventionally employed in aqueous base paints. Homopolymers of ethylene, isobutylene, and styrene, and copolymers of one or more of these hydrocarbons with one or more esters, nitriles or amides of acylic acid or of methacrylic acid or with vinyl esters, such as vinyl acetate and vinyl chloride, or with vinylidene chloride are also used. The diene polymers are generally used in aqueous base paints in the form of copolymers with one or more monomers following: styrene, vinyltoluene, acrylonitrile, methacrylonitrile, and the abovementioned esters of acrylic acid or methacrylonitrile, and the abovementioned esters of acrylic acid or methacrylic acid. It is also quite common to include a small amount, such as 1/2 to 2.5% or more, of an acid monomer in the monomer mixture used for making the copolymers for all three general types mentioned above by emulsion polymerzation. Acids used include acrylic, methacrylic, itaconic, aconitic, citraconic, crotonic, maleic, fumaric, the dimer of acrylic acid, and so on.
These aqueous dispersions as the emulsion polymer in the paint may be made using one or more emulsifiers of anionic, cationic, or non-ionic type. Mixtures of two or more emulsifiers rgardless of type may be used, except that it is generally undesirable to mix a cationic with an anionic type in any appreciable amounts since they tend to neutralize each other. The amount of emulsifier may range from about 0.1 to 6% by weight or sometimes even more, based on the weight of the total monomer charge. When using a persulfate type of initiator, the addition of emulsifiers is often unnecessary and this omission or the use of only a small amount, e.g., less than about 0.5%, of emulsifier, may sometimes be desirable from the cost standpoint (elimination of expensive emulsifier), and less sensitivity of the dried coating or impregnation to moisture, and hence less liability of the coated substrate to be affected by moisture, which, for instance, would produce coatings less liable to swelling or softening, particularly when subjected to humid atmospheres. The average particle size or diameter of these dispersed polymers may be from about 0.03 to 3 microns or even larger. The particle size, whenever referred to herein, is the "weight average diameter." This number, expressed in microns, is determined using the ultra-centrifuge. A description of the method can be found in the Journal of Colloid Science 15, pp. 563-572, 1960 (J. Brodnyan). In general, the molecular weights of these emulsion polymers are high, e.g., from about 100,000 to 10 million viscosity average, most commonly above 500,000.
In general, a gallon of emulsion paint is comprised of about 0.5 to 3 lbs. of film-forming resin and about 0.2 to about 5 lbs. of finely-divided pigment. Typical pigments are titanium dioxide and other titanium pigments, white lead, zinc, oxide, zinc sulfide, barium sulfate, calcium carbonate, lithopone, silica, talc, mica, clays, iron oxide, carbon black, cadmium sulfide, toluidene red, chrome orange, chrome yellow, chrome green, and others known in the artm. Tyical latices of film-forming resins are those of the alkyl acrylates and methacrylates, vinyl acetate, styrene-butadiene, and others known in the art. Minor amounts of other coatings additives may be included in the paint formulations, for example, antifoams, mildewcides, thickeners, wetting agents, bacteriostats, etc.
Another aspect of the invention is the provision of dispersions of pigments as fluid pastes of high solids content and low aqueous media content (said aqueous media comprising water or water and a minor or major proportion of alkylene glycol as aforementioned) containing in admixture a relatively minor amount of the described water-soluble salt of the copolymer of ethylenically unsaturated acid and the hydroxyalkyl ester thereof as dispersant. The amount of the salt of the copolymer effecting dispersion of solids and fluidity of the pigment paste will usually not be over about three percent of the weight of pigment and may be as low as about 0.05%.
For the preparation of these pigment pastes, it is generally most convenient to prepare an aqueous solution of copolymer in salt form. Concentrations of 5 to 40% may be used, although those of 10 to 20% are usually preferred. Pigment, water (including an alkylene glycol), and solutions are mixed. If desired, the paste or suspension may be ground in a mill--a pebble mill, roll mill, colloid mill, or high speed stone mill, or in some instances a high shear mixer being suitable. Sufficient copolymer is used to ensure good dispersion and fluidity of the paste. The optimum amount of copolymer will depend upon the specific pigmement or pigments and upon the state of subdivision thereof. In general, the finer the particle size the more dispersant should be used. Concentrated pastes can be extended to give dilute pastes, when the latter are needed. The pigment pastes are a suitable and convenient composition for addition to aqueous resin latexes or dispersions, as previously discussed, to form emulsion paints. Moreover, fluid pastes of certain pigments have diverse uses, for example, such high solids content slurries of calcium hydroxide are useful for coatings as white-wash, field markings, or the like, or as concentrated alkaline reagents in chemical manufacturing; dispersions of carbon blacks in aqueous media are useful in the fields of paper, cement, water-base paints, coating compositions, inks, rayons, and rubber. The pigments may be present in the foregoing pastes in an amount up to 85% by weight of the paste.
In the representative examples next presented, the following abbreviations are used for the sake of brevity;
MAA: methacrylic acid
AA: acrylic acid
HEMA: 2-hydroxyethyl methacrylate
HMPA: 2-hydroxypropyl methacrylate
DHPMA: 2,3-dihydroxypropyl methacrylate
BMA: N-butyl methacrylate
Various illustrative processes for preparing the copolymer dispersants used in the invention are as follows.
A two-liter, four-necked, round bottomed flask fitted with stirrer, reflux condenser, heating mantle, two additional funnels and nitrogen inlet, is charged with 348 g. isopropanol which is heated to reflux under nitrogen. A monomer mixture of 143 g. HEMA and 94.6 g. glacial MAA is added simultaneously over a one hour period with the addition of a solution of 18.8 g. "Lupersol 11" (57% t-butyl peroxypivalate) in 94 g. isopropanol while maintaining the reactor contents at reflux (84° C.). Reflux is maintained for another hour. The resulting polymer solution (36.3% solids, viscosity=1825 centipoise, Brookfield LV #2, 12 rpm) is added gradually along with addition of equivalent amounts of 50% NaOH solution (to maintain homogeneity) to 300 g. water heated to reflux in a similar reaction vessel fitted with a distillation head. Isopropanol and water are distilled off until the vapor temperature reaches 100° C. The pH of the clear colorless product is adjusted to 9.6 with additional caustic solution, and solids concentration is diluted to 25% (solution viscosity=39.5 cps., LV #2, 60 rpm). The dissolved copolymer is composed of HEMA/MAA in a 60/40 weight ratio.
A reaction flask as described above is charged with 300 g. propylene glycol which is heated to 150° C. under nitrogen blanket. A solution of 210 g. HEMA, 90 g. MMA, 3 g. mercaptoethanol and 12 g. "Lupersol 70" (75% t-butyl peracetate) is added over a five hour period while maintaining temperature at 150° C. Addition of 1.2 g. more of "Lupersol 70" without exotherm indicates completion of reaction; however, heating is continued for 30-45 minutes.
Vacuum is applied and about 160 g. propylene glycol is removed at 120° C./30 mm Hg. The contents are cooled to 50° C. and 50% aqueous NaOH is added gradually until the pH of the solution is 9.2. The copolymer solution, adjusted to 50% solids concentration by water addition, contains 19% propylene glycol. Its appearance is light amber, viscosity=1,000 cps. (LV #2, 6 rpm); adjusted to 25% solids, viscosity=16 cps. The dissolved copolymer is composed of HEMA/MMA in a 70/30 weight ratio.
A five-liter flask equipped as those described above is charged with 1955 g. water and 567.3 g. propylene glycol and the solution heated to 90° C. while sparging with nitrogen. 45% of a catalyst solution of 62.5 g. ammonium persulfate in 312.5 g. water is added, and then the remainder of the catalyst solution and 480.75 g. MAA and 1121.75 g. HEMA are added simultaneously over a 1.5 hours period. The reaction mixture is held at 92°-95° C. for an additional hour. The viscosity of the mixture is 82.5 cps. (LV, #2, 60 rpm).
The mixture is cooled and 430 g. of 50% aqueous NaOh are added gradually to give a pH of 9.6. The propylene glycol content of the solution is 11.2%, dissolved solids content is 42%, viscosity 360 cps. (LV #2, 30 rpm); when diluted to 25% solids, viscosity is 23 centipoise. The dissolved copolymer is composed HEMA/MAA in a 70/30 weight ratio.
Various copolymer compositions are thus prepared according to the one of the above processes, as summarized in Table I below.
TABLE I
__________________________________________________________________________
Monomers in
Copolymer, and
Process Product Solution (Na.sup.- Salt)
Example No.
Weight Ratios Polymerization
pH
% Solids
Viscosity Cps.
__________________________________________________________________________
1 (control)
MAA C 9.7
25 40
2 HEMA/MAA.
30/70
A 9.7
25 36
3 " 50/50
B 9.5
25 20
4 " 50/50
C 9.5
25 31
5 " 60/40
A 9.6
25 40
6 " 60/40
B 9.1
25 13
7 " 60/40
C 9.2
25 30
8 " 70/30
B 9.2
25 16
9 " 70/30
C 9.6
25 23
10 " 70/30
C 9.5
25 27
(NH.sup.- salt of
Exp. 9)
11 " 75/25
C 9.3
25 27
12 " 80/20
A 9.1
25 28
13 HPMA/MAA.
70/30
B 9.2
25 12
14 HEMA/AA. 60/40
A 9.7
35 28
15 " 80/20
A 9.5
26 25
16 *DHPMA/MAA.
30/70
C 9.5
35 856
17 " 50/50
C 9.5
35 498
18 " 70/30
C 9.8
35 210
19 BMA/HEMA/
32/29/39
A 9.1
35 125
MAA
__________________________________________________________________________
*DHPMA introduced as isopropylidene glycerol methacrylate and allowed to
hydrolyze to DHPMA in situ
The above described polymers, along with an additional prior art control U.S. Pat. No. 2,930,775), are evaluated as pigment dispersants to produce semigloss latex paints in accordance with the general formulation given below. All components are maintained in equal proportion with the exception of pigment dispersant level which is specified in Table II as a percentage based on total pigment weight.
The following ingredients in parts by weight are charged to a suitable steel vessel and ground in a Cowles dissolver (high speed dispersing mill) at about 4,000 peripheral feet per minute for 20 minutes to prepare a pigment paste.
______________________________________
Propylene glycol 60.0
Polymeric dispersant in water
9.2
Water 5.1
Zinc Oxide 25.0
Rutile Titanium Dioxide
250.0
Nopoc "NXZ" antifoaming agent
1.0
Octylphenoxypolyethoxyethanol
2.5
(OPE).sub.9-10 (surfactant)
Tert-butylaminoethanol
3.7
(wetting agent)
______________________________________
The dispersions are then "let-down" at a lower speed with:
______________________________________
Water 30.0
Propylene glycol 38.0
Eastman "Texanol" coalescing
25.0
aid (pentanediol monoisobutyrate)
Nopco "NXZ" antifoaming agent
1.0
2-N--octyl-4-isothiazolin-3-one,
2.0
45% active ingredient (mildew-
cide)
Hercules "Natrosol 250 MR"
72.7
hydroxyethyl cellulose thickener,
3% active ingredient in water
Acrylic copolymer latex (50.7%
546.7
Methyl methacrylate, 1.3% methyl
acrylate, 48% butyl acrylate, 46%
solids. pH 9.5)
______________________________________
The paint formulations are evaluated for the critical properties of specular gloss, viscosity at high and low shear rate, and stability thereof when subjected to elevated temperature and to freeze-thaw cycling in accordance with the following procedures.
______________________________________
Specular gloss: ASTM D523-67 (reapproved
1972)
Low Shear Viscosity:
Stormer viscosity (KU),
ASTM D562-55 (reapproved
1972)
High Shear Viscosity:
ICI Cone and Plate (poise),
Research Equipment (London),
Ltd.
Stability Conditions:
(Closed paint cans)
Equilibrated: 240 hours at room tempera-
ture
Heat Aged: 240 hours at 140° F.
Freeze thaw: 5 cycles wherein one cycle
is 16 hours at -10° C.,
followed by 8 hours at room
temperature.
______________________________________
All formulations are sheared by shaking for 15 minutes on a Red Devil paint mixer prior to measuring viscosity.
Test results are summarized In Table II, below.
TABLE II
__________________________________________________________________________
Stormer Viscosity
Brushing Viscosity
60° Gloss
(Low Shear, KU)
(High Shear, ICI)
Formulation
Dispersant
% Dispersant
Heat aged
equili-
Heat
freeze-
equili-
Heat
freeze-
No. (of example)
(on pigment)
sample
Init.
brated
aged
thaw
brated
aged
thaw
__________________________________________________________________________
a 1 (control)
1.0 25 71 70 67 80 1.1 1.1
1.1
b Control*
1.0 55 75 70-gel
gel
gel ˜2+
gel
gel
(Initial)
(var.
results)
c 2 1.0 43 72 72 69 72 1.2 1.0
1.2
1.1 36 72 72 63 72 1.2 1.1
1.1
d 3 1.0 48 70 72 72 79 1.3 1.1
1.4
1.8 43 70 72 72 77 1.0 1.0
1.1
e 4 1.0 54 72 67 67 67 1.0 1.0
1.1
f 5 1.0 56 72 74 67 72 1.3 1.1
1.2
1.7 51 72 76 69 72 1.2 1.1
1.2
g 6 1.0 52 72 72 77 79 1.0 1.1
1.1
2.2 45 72 72 72 79 1.1 1.0
1.2
h 7 1.0 59 74 67 67 72 1.1 1.1
1.1
i 8 1.0 64 70 72 77 87 1.2 1.3
1.3
2.7 60 70 72 67 79 1.1 1.1
1.1
j 9 1.0 67 83 82 82 77 1.2 1.2
1.3
1.5 62 72 72 77 82 1.1 1.1
1.1
2.0 55 72 72 67 77 1.2 1.1
1.1
2.5 53 72 72 67 72 1.1 1.1
1.1
k 10 2.5 43 -- 77 72 77 1.2 1.1
1.2
m 11 1.0 66 86 82 82 80 1.3 1.3
1.4
n 12 1.0 56 95 72 69 82 1.4 1.3
1.4
2.5 64 89 69 67 72 1.0 1.1
1.1
o 13 2.4 70 75 82 77 82 1.2 1.3
1.3
p 14 1.0 57 72 79 67 86 1.3 2.5
1.2
1.7 52 72 77 72 76 1.2 1.1
1.2
q 15 1.0 45 89 79 86 >141
1.5 1.8
2.0
3.0 59 89 82 67 88 1.3 1.3
1.6
r 16 1.0 47 74 67 67 67 1.1 1.0
1.0
s 17 1.0 57 77 67 67 72 1.1 1.0
0.9
t 18 1.0 67 86 86 82 82 1.2 1.2
1.2
u 19 1.0 58 82 82 77 84 1.3 1.2
1.3
__________________________________________________________________________
*This control is the sodium salt of diisobutylenemaleic copolymer
anhydride (1:1 mole ratio) described by Fordyce et al. U.S. Pat. No.
2,930,775
All paints with the present dispersants exhibit excellent viscosity stability. A steady improvement in specular gloss with increasing nonionic comonomer content is observed; however, excessive nonionic comonomer content leads to poor stability if used at inadequate levels (Formulation q). Very poor gloss is found with the methacrylic acid control dispersant (Formulation a). Very poor stability is found with the other control dispersant (Formulation b).
In all cases except Formulation b, adhesion of the test paints to a glossy oil based alkyl paint (duPont Outside Trim and Shutter Gloss Enamel, Code 801C Light Green) is excellent.
In a test for foaming tendency, dispersant samples are diluted to 5 weight percent solids with water and shaken vigorously in jars. With the exception of the control dispersant used in Formulation b, all of the materials confer little or no foaming tendency.
Claims (31)
1. An improved aqueous emulsion paint comprising a mixture of a film-forming latex polymer and a pigment dispersion, containing as dispersant, from about 0.01 to about 5%, based on pigment weight, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 15,000 consisting essentially of polymerized units of (A) 45 to 90 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 10 to 55 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the half ester or half amide of itaconic acid..].
2. A paint according to claim .[.1.]. .Iadd.48 .Iaddend.containing from about 0.1 to about 2 pounds per gallon of paint, of ethylene glycol, propylene glycol of hexylene glycol, about 0.5 to 3 pounds of film-forming latex polymer per gallon of paint and about 0.2 to about 5 pounds of pigment per gallon of paint.
3. A paint in accordance with claim .[.1.]. .Iadd.48 .Iaddend.wherein the copolymer dispersant has a number average molecular weight of from about 1,000 to about 10,000, component (A) is 55 to .[.80%.]. .Iadd.75% .Iaddend.and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydropropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate; and component (b) is .[.20.]. .Iadd.25 .Iaddend.to 45% and is selected from the group consisting of acrylic acid and methacrylic acid.
4. A paint in accordance with claim 3 containing from about 0.5 to 1.3 pounds per gallon of paint of ethylene glycol, propylene glycol or hexylene glycol.
5. A paint in accordance with claim 3 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxyethyl methacrylate, and component (B) is 25 to 40% and is methacrylic acid.
6. A paint in accordance with claim 3 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxypropyl methacrylate, and component (B) is 25 to 40% and is methacrylic acid.
7. A paint in accordance with claim 3 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2,3-dihydroxypropyl methacrylate, and component (B) is 25 to 40%, and is methacrylic acid.
8. A paint in accordance with claim 4 in which the salt of the copolymer is the sodium salt.
9. A paint in accordance with claim 4 in which the salt of the copolymer is the ammonium salt. .[.10. A method for improving the properties and performance of an aqueous emulsion paint comprising a mixture of a film-forming latex polymer and a pigment dispersion which comprises incorporation therein as pigment dispersant, from about 0.01 to about 5%, based on pigment weight of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 15,000 consisting essentially of polymerized units of (A) 45 to 90 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 10 to 55 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the half ester or half amide
thereof..]. 11. A method according to claim .[.10.]. .Iadd.49 .Iaddend.wherein the paint emulsion contains from about 0.1 to about 2 pounds per gallon of paint of ethylene glycol, propylene glycol or hexylene glycol, about 0.5 to 3 pounds of film-forming latex polymer per gallon of paint and about 0.2 to about 5 pounds of pigment per gallon of
paint. 12. A method in accordance with claim .[.10.]. .Iadd.49 .Iaddend.wherein the copolymer dispersant has a number average molecular weight of from about 1,000 to 10,000, component (A) is 55 to .[.80%.]. .Iadd.75% .Iaddend.and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate; and component (B) is .[.20.].
.Iadd.25 .Iaddend.to 45%, and acrylic acid or methacrylic acid. 13. A method in accordance with claim 12 wherein the paint emulsion contains from about 3.5 to 1.3 pounds per gallon of paint of ethylene glycol,
propylene glycol and hexylene glycol. 14. A method in accordance with claim 12 wherein the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxyethyl methacrylate, and component (B) is
25 to 40% and is methacrylic acid. 15. A method in accordance with claim 12 wherein the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxypropyl methacrylate, and component (B) is 25 to
40% and is methacrylic acid. 16. A method in accordance with claim 12 wherein the salt of the copolymer is the sodium salt, comonent (A) is 60 to 75% and is 2,3-hydroxypropyl methacrylate, and component (B) is 25 to
40% and is methacrylic acid. 17. A method in accordance with claim 13
wherein the salt of the copolymer is the sodium salt. 18. A method in accordance with claim 13 wherein the salt of the copolymer is the ammonium salt. .[.19. A method of dispersing a finely divided pigment in water, comprising the step of mixing said pigment with water and, with about 0.01 to about 5%, based on physical weight, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 15,000 consisting essentially of polymerized units of (A) 45 to 90 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 10 to 55 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the half ester or
half amide or itaconic acid..]. 20. The method of claim .[.19.]. .Iadd.50 .Iaddend.in which said copolymer dispersant has a number average molecular weight of from about 1,000 to about 10,000, component (A) is 55 to .[.90%.]. .Iadd.75% .Iaddend.and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate; and component (B) is .[.20.]. .Iadd.25 to 45% and is selected from acrylic acid and methacrylic acid, and said acid water contains up to 2 pounds of a glycol per gallon. .[.21. A pigment paste comprising a water-based suspension of finely-divided pigment dispersed with about 0.05% to about 3%, on the weight of pigment, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 1,000 to about 10,000 consisting essentially of polymerized units of (A) 45 to 90 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 10 to 55 weight percent of acrylic or methacrylic acid..].
2. .[.A paste.]. .Iadd.The method .Iaddend.in accordance with claim .[.19.]. .Iadd.58 .Iaddend.which contains ethylene glycol, propylene
glycol or hexylene glycol. 23. A paste in accordance with claim .[.19.]. .Iadd.50 .Iaddend.wherein the copolymer dispersant has a number average molecular weight of from about 2,000 to 7,000, component (A) is 55 to .[.80%.]. .Iadd.75% .Iaddend.and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate; and component (B) is 20 to
45%. 24. A .[.plate.]. .Iadd.paste .Iaddend.in accordance with claim .[.21.]. .Iadd.51 .Iaddend.which contains ethylene glycol, propylene
glycol or hexylene glycol. 25. A paste in accordance with claim 22 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxyethyl methacrylate, and component (B) is 25 to 40% and
is methacrylic acid. 26. A paste in accordance with claim 22 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2-hydroxypropyl methacrylate, and comonent (B) is 25 to 40% and is
methacrylic acid. 27. A paste in accordance with claim 22 in which the salt of the copolymer is the sodium salt, component (A) is 60 to 75% and is 2,3-dihydroxypropyl methacrylate, and component (B) is 25 to 40% and is
methacrylic acid. 28. A paste in accordance with claim 22 in which the
salt of the copolymer is the sodium salt. 29. A paste in accordance with claim 22 in which the salt of the copolymer is the ammonium salt.
.Iadd. An improved aqueous emulsion paint comprising a mixture of film-forming latex polymer and a pigment dispersion, containing as dispersant, from about 0.01 to about 5%, based on pigment weight, of a water-soluble alkai metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 5,000 consisting essentially of polymerized units of (A) 29 to 75 weight percent of a hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 25 to 70 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the half ester or half amide of itaconic acid. .Iaddend. .Iadd.31. A paint in accordance with claim 30 wherein the copolymer dispersant has a number average molecular weight of from about 1,000 to about 10,000, component (A) and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate and is selected from the group consisting of
acrylic acid and methacrylic acid. .Iaddend. .Iadd.32. A method for improving the properties and performance of an aqueous emulsion paint comprising a mixture of a film-forming latex polymer and a pigment dispersion which comprises incorporation therein as pigment dispersant, from about 0.01 to about 5%, based on pigment weight of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 15,000 consisting essentially of polymerized units of (A) 29 to 75 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 25 to 70 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the half ester or half amide thereof. .Iaddend. .Iadd.33. A method in accordance with claim 32 wherein the copolymer dispersant has a number average molecular weight of from about 1,000 to 10,000 component (A) selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate; and component (B) is acrylate acid or methacrylic acid. .Iaddend. .Iadd.34. A method of dispersing a finely divided pigment in water, comprising the step of mixing said pigment with water and, with about 0.01 to about 5%, based on physical weight, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 500 to about 15,000 consisting essentially of polymerized units of (A) 29 to 75 weight percent of hydroxyalkyl ester of acrylic acid or methacrylic percent of hydroxyalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 25 to 70 weight percent of acrylic acid, methacrylic acid, itaconic acid, or the
half amide of itaconic acid. .Iaddend. .Iadd.35. The method of claim 34 in which said copolymer dispersant has a number average molecular weight of from about 1,000 to about 10,000, component (A) and is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate and is selected from acrylic acid and methacrylic acid, and said water contains up to 2 pounds of a glycol per gallon. .Iaddend. .Iadd.36. A pigment paste comprising a water-based suspension of finelydivided pigment dispersed with about 0.05% to about 3%, on the weight of pigment, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight of pigment, of a water-soluble alkali metal, ammonium, or amine salt of a copolymer having a number average molecular weight in the range of about 1,000 to 10,000 consisting essentially of polymerized units of (A) 45 to 75 weight percent of a hydroxylalkyl ester of acrylic acid or methacrylic acid, wherein the alkyl group of the ester moiety has from two to six carbon atoms; and (B) 25 to 70 weight percent of acrylic acid methacrylic acid, itaconic acid, or the half ester or half amide of itaconic acid. .Iaddend. .Iadd.37. A paste in accordance with claim 36 wherein the copolymer dispersant has a number average molecular weight of from about 2,000 to 7,000, component (A) selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3,-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate. .Iaddend.
.Iadd.38. A paste in accordance with claim 24 in which the salt of the copolymer is the sodium salt, component (A) is 2-hydroxyethyl methacrylate, and component (B) is methacrylic acid. .Iaddend. .Iadd.39. A paste in accordance with claim 24 in which the salt of the copolymer is the sodium salt, component (A) is 2-hydroxypropyl methacrylate, and component (B) is methacrylic acid. .Iaddend. 40. A paste in accordance with claim 24 in which the salt of the copolymer is the sodium salt, component (A) is 2,3-dihydroxypropyl methacrylate, and component (B) is methacrylic acid. .Iadd.41. A paste in accordance with claim 36 in which the salt of the copolymer is the sodium salt. .Iaddend. .Iadd.42. A paste in accordance with claim 36 in which the salt of the copolymer is the ammonium salt. .Iaddend. .Iadd.43. A paste in accordance with claim 41 in which compound (A) is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate, and component (B) is acrylic acid or methacrylic acid. .Iaddend. .Iadd.44. A paste in accordance with claim 42, in which compound (A) is selected from the group consisting of 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2,3-dihydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 2,3-dihydroxypropyl acrylate, and component (B) is acrylic
acid or methacrylic acid. .Iaddend. .Iadd.45. A paint in accordance with claim 10 in which up to 30% of an optional monomer selected from methyl acrylate or methacrylate, ethyl acrylate or methacrylate, n-butyl acrylate or methacrylate, sec-butyl acrylate or methacrylate, isobutyl acrylate or methacrylate, tertiary butyl acrylate or methacrylate, acrylamide, acrylonitrile, or diacetone acrylamide is included among the polymerized monomers, with the proviso that they are used in such limited amounts as to not affect the solubility of the copolymer. .Iaddend. .Iadd.46. A method according to claim 1 in which up to 30% of an optional monomer selected from methyl acrylate or methacrylate, ethyl acrylate or methacrylate, n-butyl acrylate or methacrylate, sec-butyl acrylate or methacrylate, isobutyl acrylate or methacrylate, tertiary butyl acrylate or methacrylate, acrylamide, acrylonitrile, or diacetone acrylamide is included among the polymerized monomers, with the proviso that they are used in such limited amounts as to not affect the solubility of the copolymer. .Iaddend. .Iadd.47. A pigment paste according to claim 23 in which up to 30% of an optional monomer selected from methyl acrylate or methacrylate, ethyl acrylate or methacrylate, n-butyl acrylate or methacrylate, sec-butyl acrylate or methacrylate, isobutyl acrylate or methacrylate, tertiary butyl acrylate or methacrylate, acrylamide, acrylonitrile, or diacetone acrylamide is included among the polymerized monomers, with the proviso that they are used in such limited amounts as to not affect the solubility of the copolymer. .Iaddend.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/536,821 USRE31936E (en) | 1977-01-07 | 1983-09-27 | Dispersing paint pigments |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/757,718 US4102843A (en) | 1977-01-07 | 1977-01-07 | Dispersing paint pigments |
| US613279A | 1979-01-24 | 1979-01-24 | |
| US06/536,821 USRE31936E (en) | 1977-01-07 | 1983-09-27 | Dispersing paint pigments |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/757,718 Reissue US4102843A (en) | 1977-01-07 | 1977-01-07 | Dispersing paint pigments |
| US613279A Continuation | 1977-01-07 | 1979-01-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE31936E true USRE31936E (en) | 1985-07-02 |
Family
ID=27358048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/536,821 Expired - Lifetime USRE31936E (en) | 1977-01-07 | 1983-09-27 | Dispersing paint pigments |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE31936E (en) |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4836966A (en) | 1984-03-15 | 1989-06-06 | Isoo Shimuzu | Binder for ceramics |
| US4968734A (en) * | 1986-07-01 | 1990-11-06 | W. R. Grace & Co.-Conn. | Cement admixture |
| US5124393A (en) * | 1989-08-29 | 1992-06-23 | Union Oil Company Of California | Latex paints |
| US5134186A (en) * | 1989-08-29 | 1992-07-28 | Union Oil Company Of California | Latex paints |
| US5157071A (en) * | 1989-08-29 | 1992-10-20 | Union Oil Company Of California | Paints and polymers for use therein |
| US5183504A (en) * | 1990-05-21 | 1993-02-02 | Nippon Paint Co., Ltd. | Aqueous coating composition |
| US5212225A (en) * | 1989-08-29 | 1993-05-18 | Rohm And Haas Company | Binder synthesis process |
| US5213901A (en) * | 1989-08-29 | 1993-05-25 | Rohm And Haas Company | Coated articles |
| US5219917A (en) * | 1989-08-29 | 1993-06-15 | Rohm And Haas Company | Latex-paints |
| US5227423A (en) * | 1989-08-29 | 1993-07-13 | Rohm And Haas Company | Paints and binders for use therein |
| US5276096A (en) * | 1991-08-28 | 1994-01-04 | Basf Corporation | Two package coating composition comprising a polycarbodimide with improved rheology control |
| US5276075A (en) * | 1991-10-30 | 1994-01-04 | Binney & Smith Inc. | Washable acrylic paint |
| US5356988A (en) * | 1991-07-17 | 1994-10-18 | Cargill, Incorporated | Acrylic polymer aqueous dispersion made through a micro dispersion |
| US5663224A (en) * | 1991-12-03 | 1997-09-02 | Rohm And Haas Company | Process for preparing an aqueous dispersion |
| US6080802A (en) | 1991-12-03 | 2000-06-27 | Rohm And Haas Company | Process for preparing an aqueous dispersion of composite particles including polymeric latex adsorbed to titanium dioxide |
| US6548596B1 (en) * | 1997-09-08 | 2003-04-15 | Rohm And Haas Company | Polymer compositions |
| US6869996B1 (en) | 1999-06-08 | 2005-03-22 | The Sherwin-Williams Company | Waterborne coating having improved chemical resistance |
| US20050288388A1 (en) * | 2002-05-08 | 2005-12-29 | Gernon Michael D | Compositions providing physical biocide synergist activity in paints, coatings, sealants and adhesives during storage |
| US20060106129A1 (en) * | 2002-05-08 | 2006-05-18 | Michael Gernon | Optimized alkanolamines for latex paints |
| US20060155022A1 (en) * | 2002-09-02 | 2006-07-13 | Anne Hupp | Aqueous pigment pastes containing metallic pigments and the use thereof for producing substances for decorative aqueous coatings |
| US20070135567A1 (en) * | 2004-10-08 | 2007-06-14 | Ruhoff Philip J | Self crosslinking waterborne coatings |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2930775A (en) * | 1958-10-14 | 1960-03-29 | Rohm & Haas | Pigment pastes containing water-soluble diisobutylene-maleic anhydride copolymer salts |
| GB998380A (en) * | 1960-10-05 | 1965-07-14 | Nopco Chem Co | Anionic copolymers |
| US3230275A (en) * | 1962-08-30 | 1966-01-18 | Soto Chemical Coatings Inc De | Interpolymers comprising acrylamide and a hydroxy-substituted monomer and heat curable resin compositions therewith |
| US3646099A (en) * | 1967-10-12 | 1972-02-29 | Uniroyal Inc | Cyano containing oligomers |
| US3840487A (en) * | 1971-06-03 | 1974-10-08 | Allied Colloids Mfg | Aqueous emulsion paint employing novel low molecular weight acrylic polymer dispersing agents to achieve higher gloss |
| US3859260A (en) * | 1967-10-12 | 1975-01-07 | Leland E Dannals | Oligomers |
| JPS5011440A (en) * | 1973-06-01 | 1975-02-05 | ||
| US3957711A (en) * | 1974-12-20 | 1976-05-18 | Celanese Coatings & Specialties Company | Dispersion polymerization process using hydroxyalkyl acrylate as protective colloids |
| US3980602A (en) * | 1975-02-28 | 1976-09-14 | E. I. Du Pont De Nemours And Company | Acrylic polymer dispersant for aqueous acrylic coating compositions |
| US3985698A (en) * | 1974-02-26 | 1976-10-12 | Kansai Paint Company, Ltd. | Method for improving emulsion paint by adding an acrylic resin produced from a tertiary amine containing ethylenically unsaturated monomer |
-
1983
- 1983-09-27 US US06/536,821 patent/USRE31936E/en not_active Expired - Lifetime
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2930775A (en) * | 1958-10-14 | 1960-03-29 | Rohm & Haas | Pigment pastes containing water-soluble diisobutylene-maleic anhydride copolymer salts |
| GB998380A (en) * | 1960-10-05 | 1965-07-14 | Nopco Chem Co | Anionic copolymers |
| US3223751A (en) * | 1960-10-05 | 1965-12-14 | Nopco Chem Co | Treating agents comprising carboxyl containing copolymers and amino resin or amino resin base |
| US3230275A (en) * | 1962-08-30 | 1966-01-18 | Soto Chemical Coatings Inc De | Interpolymers comprising acrylamide and a hydroxy-substituted monomer and heat curable resin compositions therewith |
| US3646099A (en) * | 1967-10-12 | 1972-02-29 | Uniroyal Inc | Cyano containing oligomers |
| US3859260A (en) * | 1967-10-12 | 1975-01-07 | Leland E Dannals | Oligomers |
| US3840487A (en) * | 1971-06-03 | 1974-10-08 | Allied Colloids Mfg | Aqueous emulsion paint employing novel low molecular weight acrylic polymer dispersing agents to achieve higher gloss |
| JPS5011440A (en) * | 1973-06-01 | 1975-02-05 | ||
| US3985698A (en) * | 1974-02-26 | 1976-10-12 | Kansai Paint Company, Ltd. | Method for improving emulsion paint by adding an acrylic resin produced from a tertiary amine containing ethylenically unsaturated monomer |
| US3957711A (en) * | 1974-12-20 | 1976-05-18 | Celanese Coatings & Specialties Company | Dispersion polymerization process using hydroxyalkyl acrylate as protective colloids |
| US3980602A (en) * | 1975-02-28 | 1976-09-14 | E. I. Du Pont De Nemours And Company | Acrylic polymer dispersant for aqueous acrylic coating compositions |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4836966A (en) | 1984-03-15 | 1989-06-06 | Isoo Shimuzu | Binder for ceramics |
| US4968734A (en) * | 1986-07-01 | 1990-11-06 | W. R. Grace & Co.-Conn. | Cement admixture |
| US5124393A (en) * | 1989-08-29 | 1992-06-23 | Union Oil Company Of California | Latex paints |
| US5134186A (en) * | 1989-08-29 | 1992-07-28 | Union Oil Company Of California | Latex paints |
| US5157071A (en) * | 1989-08-29 | 1992-10-20 | Union Oil Company Of California | Paints and polymers for use therein |
| US5212225A (en) * | 1989-08-29 | 1993-05-18 | Rohm And Haas Company | Binder synthesis process |
| US5213901A (en) * | 1989-08-29 | 1993-05-25 | Rohm And Haas Company | Coated articles |
| US5219917A (en) * | 1989-08-29 | 1993-06-15 | Rohm And Haas Company | Latex-paints |
| US5227423A (en) * | 1989-08-29 | 1993-07-13 | Rohm And Haas Company | Paints and binders for use therein |
| US5183504A (en) * | 1990-05-21 | 1993-02-02 | Nippon Paint Co., Ltd. | Aqueous coating composition |
| US5356988A (en) * | 1991-07-17 | 1994-10-18 | Cargill, Incorporated | Acrylic polymer aqueous dispersion made through a micro dispersion |
| US5380771A (en) * | 1991-07-17 | 1995-01-10 | Cargill Incorporated | Aqueous dispersion of amine salts of an acrylic polymer |
| US5276096A (en) * | 1991-08-28 | 1994-01-04 | Basf Corporation | Two package coating composition comprising a polycarbodimide with improved rheology control |
| US5276075A (en) * | 1991-10-30 | 1994-01-04 | Binney & Smith Inc. | Washable acrylic paint |
| US5663224A (en) * | 1991-12-03 | 1997-09-02 | Rohm And Haas Company | Process for preparing an aqueous dispersion |
| US6080802A (en) | 1991-12-03 | 2000-06-27 | Rohm And Haas Company | Process for preparing an aqueous dispersion of composite particles including polymeric latex adsorbed to titanium dioxide |
| US6548596B1 (en) * | 1997-09-08 | 2003-04-15 | Rohm And Haas Company | Polymer compositions |
| US6869996B1 (en) | 1999-06-08 | 2005-03-22 | The Sherwin-Williams Company | Waterborne coating having improved chemical resistance |
| US20050288388A1 (en) * | 2002-05-08 | 2005-12-29 | Gernon Michael D | Compositions providing physical biocide synergist activity in paints, coatings, sealants and adhesives during storage |
| US20060106129A1 (en) * | 2002-05-08 | 2006-05-18 | Michael Gernon | Optimized alkanolamines for latex paints |
| US7553882B2 (en) * | 2002-05-08 | 2009-06-30 | Taminco | Compositions providing physical biocide synergist activity in paints, coatings, sealants and adhesives during storage |
| US20060155022A1 (en) * | 2002-09-02 | 2006-07-13 | Anne Hupp | Aqueous pigment pastes containing metallic pigments and the use thereof for producing substances for decorative aqueous coatings |
| US7691933B2 (en) * | 2002-09-02 | 2010-04-06 | Basf Coatings Ag | Aqueous pigment pastes containing metallic pigments and the use thereof for producing substances for decorative aqueous coatings |
| US20070135567A1 (en) * | 2004-10-08 | 2007-06-14 | Ruhoff Philip J | Self crosslinking waterborne coatings |
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