CA2365303C - Laundry detergent compositions with certain cationically charged dye maintenance polymers - Google Patents
Laundry detergent compositions with certain cationically charged dye maintenance polymers Download PDFInfo
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- CA2365303C CA2365303C CA002365303A CA2365303A CA2365303C CA 2365303 C CA2365303 C CA 2365303C CA 002365303 A CA002365303 A CA 002365303A CA 2365303 A CA2365303 A CA 2365303A CA 2365303 C CA2365303 C CA 2365303C
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- 239000000203 mixture Substances 0.000 title claims abstract description 148
- 239000003599 detergent Substances 0.000 title claims abstract description 66
- 238000012423 maintenance Methods 0.000 title claims abstract description 40
- 229920000642 polymer Polymers 0.000 title abstract description 72
- 239000004744 fabric Substances 0.000 claims abstract description 53
- 229920001577 copolymer Polymers 0.000 claims abstract description 50
- 239000000178 monomer Substances 0.000 claims abstract description 45
- 239000004094 surface-active agent Substances 0.000 claims abstract description 26
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 23
- 239000004615 ingredient Substances 0.000 claims abstract description 18
- 239000000969 carrier Substances 0.000 claims abstract description 5
- -1 dispersibility aids Substances 0.000 claims description 62
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- 239000001257 hydrogen Substances 0.000 claims description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims description 30
- 125000002091 cationic group Chemical group 0.000 claims description 15
- 150000002431 hydrogen Chemical group 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 150000001450 anions Chemical class 0.000 claims description 9
- 229920002554 vinyl polymer Polymers 0.000 claims description 9
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 6
- 239000002304 perfume Substances 0.000 claims description 6
- 239000002689 soil Substances 0.000 claims description 6
- 229920002873 Polyethylenimine Polymers 0.000 claims description 3
- 238000013019 agitation Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 230000002070 germicidal effect Effects 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- 239000003755 preservative agent Substances 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 239000004902 Softening Agent Substances 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 239000002738 chelating agent Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 239000003605 opacifier Substances 0.000 claims description 2
- 239000003021 water soluble solvent Substances 0.000 claims description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- 230000008901 benefit Effects 0.000 abstract description 17
- 239000000975 dye Substances 0.000 description 35
- 229910052757 nitrogen Inorganic materials 0.000 description 30
- 239000007844 bleaching agent Substances 0.000 description 28
- 102000004190 Enzymes Human genes 0.000 description 18
- 108090000790 Enzymes Proteins 0.000 description 18
- 229940088598 enzyme Drugs 0.000 description 18
- 239000012190 activator Substances 0.000 description 15
- 239000007788 liquid Substances 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 239000004753 textile Substances 0.000 description 15
- 238000005406 washing Methods 0.000 description 12
- 238000004900 laundering Methods 0.000 description 11
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 10
- 150000008051 alkyl sulfates Chemical class 0.000 description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 8
- 125000004122 cyclic group Chemical group 0.000 description 8
- 125000000623 heterocyclic group Chemical group 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000000670 limiting effect Effects 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- QNIINJSIHZISAD-UHFFFAOYSA-N 1-prop-1-enyl-2H-pyridine Chemical compound CC=CN1CC=CC=C1 QNIINJSIHZISAD-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 6
- 125000002837 carbocyclic group Chemical group 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 101100490437 Mus musculus Acvrl1 gene Proteins 0.000 description 5
- 150000001204 N-oxides Chemical class 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 238000011065 in-situ storage Methods 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 102000005575 Cellulases Human genes 0.000 description 4
- 108010084185 Cellulases Proteins 0.000 description 4
- 108091005804 Peptidases Proteins 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 229960001922 sodium perborate Drugs 0.000 description 4
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 4
- 230000000087 stabilizing effect Effects 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- 102000013142 Amylases Human genes 0.000 description 3
- 108010065511 Amylases Proteins 0.000 description 3
- 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 3
- 102000035195 Peptidases Human genes 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 235000019418 amylase Nutrition 0.000 description 3
- 229940025131 amylases Drugs 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005562 fading Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 230000002538 fungal effect Effects 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000003002 pH adjusting agent Substances 0.000 description 3
- 239000006187 pill Substances 0.000 description 3
- 229920005646 polycarboxylate Polymers 0.000 description 3
- 150000004760 silicates Chemical class 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 3
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- LTMQZVLXCLQPCT-UHFFFAOYSA-N 1,1,6-trimethyltetralin Chemical compound C1CCC(C)(C)C=2C1=CC(C)=CC=2 LTMQZVLXCLQPCT-UHFFFAOYSA-N 0.000 description 2
- XWRBMHSLXKNRJX-UHFFFAOYSA-N 2-ethenyl-1-oxidopyridin-1-ium Chemical compound [O-][N+]1=CC=CC=C1C=C XWRBMHSLXKNRJX-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 108700020962 Peroxidase Proteins 0.000 description 2
- 102000003992 Peroxidases Human genes 0.000 description 2
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000005228 aryl sulfonate group Chemical group 0.000 description 2
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 229920005565 cyclic polymer Polymers 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000002979 fabric softener Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000001902 propagating effect Effects 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 2
- 239000002888 zwitterionic surfactant Substances 0.000 description 2
- SGRHVVLXEBNBDV-UHFFFAOYSA-N 1,6-dibromohexane Chemical compound BrCCCCCCBr SGRHVVLXEBNBDV-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 1
- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical class OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- JADMAVSCPFDMLP-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate;prop-2-enamide Chemical compound NC(=O)C=C.CN(C)CCOC(=O)C(C)=C JADMAVSCPFDMLP-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- GOKVKLCCWGRQJV-UHFFFAOYSA-N 2-[6-(decanoylamino)hexanoyloxy]benzenesulfonic acid Chemical compound CCCCCCCCCC(=O)NCCCCCC(=O)OC1=CC=CC=C1S(O)(=O)=O GOKVKLCCWGRQJV-UHFFFAOYSA-N 0.000 description 1
- JKZLOWDYIRTRJZ-UHFFFAOYSA-N 2-[6-(octanoylamino)hexanoyloxy]benzenesulfonic acid Chemical compound CCCCCCCC(=O)NCCCCCC(=O)OC1=CC=CC=C1S(O)(=O)=O JKZLOWDYIRTRJZ-UHFFFAOYSA-N 0.000 description 1
- KKBHSBATGOQADJ-UHFFFAOYSA-N 2-ethenyl-1,3-dioxolane Chemical compound C=CC1OCCO1 KKBHSBATGOQADJ-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- FAGGUIDTQQXDSJ-UHFFFAOYSA-N 3-benzoylazepan-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCNC1=O FAGGUIDTQQXDSJ-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- KOEDSBONUVRKAF-UHFFFAOYSA-N 4-(nonylamino)-4-oxobutaneperoxoic acid Chemical compound CCCCCCCCCNC(=O)CCC(=O)OO KOEDSBONUVRKAF-UHFFFAOYSA-N 0.000 description 1
- KRFXUBMJBAXOOZ-UHFFFAOYSA-N 4-ethenyl-1-oxidopyridin-1-ium Chemical compound [O-][N+]1=CC=C(C=C)C=C1 KRFXUBMJBAXOOZ-UHFFFAOYSA-N 0.000 description 1
- AVLQNPBLHZMWFC-UHFFFAOYSA-N 6-(nonylamino)-6-oxohexaneperoxoic acid Chemical compound CCCCCCCCCNC(=O)CCCCC(=O)OO AVLQNPBLHZMWFC-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical group [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
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- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 125000000815 N-oxide group Chemical group 0.000 description 1
- SXKQTYJLWWQUKA-UHFFFAOYSA-N O.O.O.O.O.O.O.O.O.O.OB(O)O.OB(O)O.OB(O)O.OB(O)O Chemical compound O.O.O.O.O.O.O.O.O.O.OB(O)O.OB(O)O.OB(O)O.OB(O)O SXKQTYJLWWQUKA-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 1
- 229920000691 Poly[bis(2-chloroethyl) ether-alt-1,3-bis[3-(dimethylamino)propyl]urea] Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 229920000289 Polyquaternium Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 238000010936 aqueous wash Methods 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 125000005620 boronic acid group Chemical class 0.000 description 1
- ABBZJHFBQXYTLU-UHFFFAOYSA-N but-3-enamide Chemical compound NC(=O)CC=C ABBZJHFBQXYTLU-UHFFFAOYSA-N 0.000 description 1
- CMFFZBGFNICZIS-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O CMFFZBGFNICZIS-UHFFFAOYSA-N 0.000 description 1
- HXDRSFFFXJISME-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O HXDRSFFFXJISME-UHFFFAOYSA-N 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YIOJGTBNHQAVBO-UHFFFAOYSA-N dimethyl-bis(prop-2-enyl)azanium Chemical group C=CC[N+](C)(C)CC=C YIOJGTBNHQAVBO-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- JHUXOSATQXGREM-UHFFFAOYSA-N dodecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCC(=O)OO JHUXOSATQXGREM-UHFFFAOYSA-N 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229920005684 linear copolymer Polymers 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- FODOUIXGKGNSMR-UHFFFAOYSA-L magnesium;2-oxidooxycarbonylbenzoate;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[O-]OC(=O)C1=CC=CC=C1C([O-])=O FODOUIXGKGNSMR-UHFFFAOYSA-L 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- TXXWBTOATXBWDR-UHFFFAOYSA-N n,n,n',n'-tetramethylhexane-1,6-diamine Chemical compound CN(C)CCCCCCN(C)C TXXWBTOATXBWDR-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229940044652 phenolsulfonate Drugs 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000083 poly(allylamine) Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003141 primary amines Chemical group 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 229940071207 sesquicarbonate Drugs 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0021—Dye-stain or dye-transfer inhibiting compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3792—Amine oxide containing polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The present invention relates to laundry detergent compositions providing dye protection benefits to fabric comprising: a) from about 4 % to about 70 % by weight, of a surfactant; b) from about 0.01 % by weight, of a dye maintenance polymer or oligomer, said polymer or copolymer comprising one or more linearly polymerizing monomers, cyclically polymerizing monomers, and mixtures thereof; and c) the balance carriers and adjunct ingredients.
Description
LAUNDRY DETERGENT COMPOSITIONS WITH CERTAIN CATIONICALLY CHARGED
DYE MAINTENANCE POLYMERS
FIELD OF THE INVENTION
The present invention relates to compositions, in either liquid or granular form, for use in laundry applications, wherein the compositions comprise certain dye maintenance polymers that have a net positive charge. Compositions comprising the dye maintenance polymers of this invention impart appearance and integrity benefits to fabrics and textiles laundered in washing solutions formed from such compositions.
BACKGROUND OF THE INVENTION
It is, of course, well lrnown that alternating cycles of using and laundering fabrics and textiles, such as articles of worn clothing and apparel, will inevitably adversely affect the appearance and integrity of the fabric and textile items so used and laundered. Fabrics and textiles simply wear out over time and with use. Laundering of fabrics and textiles is necessary to remove soils and stains which accumulate therein and thereon during ordinary use. However, the laundering operation itself, over many cycles, can accentuate and contribute to the deterioration of the integrity and the appearance of such fabrics and textiles.
Deterioration of fabric integrity and appearance can manifest itself in several ways. Short fibers are dislodged from woven and lrnit fabric/textile structures by the mechanical action of laundering. These dislodged fibers may form lint, fuzz or "pills" which are visible on the surface of fabrics and diminish the appearance of newness of the fabric. Further, repeated laundering of fabrics and textiles, especially with bleach-containing laundry products, can remove dye from fabrics and textiles and impart a faded, worn out appearance as a result of diminished color intensity, and in many cases, as a result of changes in hues or shades of color.
Given the foregoing, there is clearly an ongoing need to identify materials which could be added to laundry products that would associate themselves with the fibers of the fabrics and textiles laundered using such products and thereby reduce or minimize the tendency of the laundered fabric/textiles to deteriorate in appearance. Any such detergent product additive material should, of course, be able to benefit fabric appearance and integrity without unduly interfering with the ability of the laundry product to perform its intended function. The present invention is directed to the use of dye maintenance polymers in laundry applications that perform in this desired manner.
SUMMARY OF TIC INVENTION
The present invention meets the aforementioned need in that it has been surprisingly discovered that fabric which is treated, and subsequently re-treated with the compositions of the present invention, will resist normal fading and color loss without regard to the circumstances, inter alia, due to mechanical wear and abrasion. In addition, fabric which has not been treated can have the loss of fabric dye attenuated by washing clothing with the laundry detergent compositions of the present invention. The compositions of the present invention can take any form, inter alia, heavy duty liquid (HDL), heavy duty granular (HDG), bars, pastes, thixotropic compositions.
In one embodiment the present invention provides a detergent composition comprising:
a) from 4% to 70% by weight, of a surfactant; b) from 0.01 % to 10% by weight, of a dye maintenance co-polymer, said copolymer having the general formula:
A
x has the value of from 10 to 100,000; y has the value of from 10 to 100,000;
the ratio of x to y is from 9:1 to 1:9; each Z is independently (CH2)mCOR' wherein R' is selected from: i) -OR3;
ii) -O(CHz)°N(R3h; iii) -0(CHz)r,N+(R3)3X ; iv) -NR3(CHZ)°N(R3~;
v) -NR3(CHZ~,N+(R3~X ;
vi) -(CHz)"N(R3)Z; vii) -(CHZ)"N+(R3)3X-; viii) or mixtures thereof; each R3 is independently hydrogen, Cl-Cg alkyl, CZ-C$ hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6; the index m is from 0 to 6; provided said co-polymer has a net cationic charge; and wherein said dye maintenance co-polymer is not an polyethyleneimine or alkoxylated derivative thereof; and c) the balance carriers and other adjunct ingredients.
Another aspect of the present invention relates to laundry detergent compositions providing dye protection benefits to fabric comprising:
2a a) from about 4% to about 70% by weight, of a surfactant selected from the group consisting of nonionic, anionic, cationic, amphoteric, zwitterionic surfactants and mixtures thereof, preferably at least one of said surfactants is an anionic surfactant;
b) from about 0.01 %, preferably from about 0.1 %, more preferably from about 0.5%, most preferably from about 0.8% to about 10%, preferably to about 8%, more preferably to about 6%, most preferably to about 5% by weight, of a dye maintenance polymer or oligomer, said polymer or copolymer comprising one or more units having the formula:
I) linear polymer units having the formula:
R~ R2 I ~
C-C
R~ Z
wherein each R' is independently a) hydrogen;
b) C1-C4 alkyl;
c) substituted or unsubstituted phenyl;
d) substituted or unsubstituted benzyl;
e) carbocyclic;
f) heterocyclic;
g) and mixtures thereof;
eachRZ is independently a) hydrogen;
b) halogen c) C,-C4 alkyl;
d) C,-C4 alkoxy;
e) substituted or unsubstituted phenyl;
f) substituted or unsubstituted benzyl;
g) carbocyclic;
h) heterocyclic;
i) and mixtures thereof;
eachZ is independently a) hydrogen;
b) hydroxyl;
c) halogen;
d) -(CHZ),"R;
wherein R is:
i) hydrogen;
ii) hydroxyl iii) halogen;
iv) nitrilo;
v) -OR3;
vi) -O(CHZ)"N(R3)Z;
vii) -O(CHZ)"N+(R3)3X
;
viii) -OCO(CHZ)"N(R3)z;
ix) -OCO(CHZ)"N+(R3)3X
-;
x) -NHCO(CHZ)"N(R3)2;
xi) -NHCO(CHZ)"N+(R3)3X-;
xii) -(CHZ)"N(R3)z;
xiii) -(CHz)oN+(R3)sX ;
xiv) carbocyclic;
xv) heterocyclic;
xvi) nitrogen heterocycle quaternary ammonium;
xvii) nitrogen heterocycle N-oxide;
xviii) aromatic N-heterocyclic quaternary ammonium;
xix) aromatic N-heterocyclic N-oxide;
xx) -NHCHO;
xxi) or mixtures thereof;
each R3 is independently hydrogen, C,-Cg alkyl, CZ-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion;
the index n is from 0 to 6 e) -(CHZ)",COR' wherein R' is i) -OR3;
ii) -O(CHZ)nN(R3)2;
iii) -O(CHz)"N+(R3)sX
-;
iv) -NR3(CHZ)"N(R3)z;
-NR3(CHz)nN+(R3)sX
v1) -(CHZ)nN(R3)2i v11) -(CHZ)nN+(R3)sX
, viii) or mixtures thereof;
each R3 is independently hydrogen, C,-Cg alkyl, CZ-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion;
the index n is from 0 to 6;
f) and mixtures thereof;
the index m is from 0 to 6;
II) cyclic units derived from cyclically polymerizing monomers having the formula:
Ra _ X
Ra-N~ Rs Rs wherein each R4 is independently an olefin comprising unit which is capable of propagating polymerization in addition to forming a cyclic residue with an adjacent R4 unit; RS is C,-C,2 linear or branched alkyl, benzyl, substituted benzyl, and mixtures thereof; X is a water soluble anion; and III) mixtures thereof;
provided said polymer or co-polymer has a net cationic charge; and wherein said dye maintenance polymer is not an polyethyleneimine or alkoxylated derivative thereof; and b) the balance carriers and other adjunct ingredients.
In addition to the surfactant and the dye maintenance polymer of this invention, the laundry detergent compositions herein comprise from about 0.01% to 80% by weight of an organic or inorganic detergency builder and other conventional laundry detergent products.
In its method aspect, the present invention relates to the laundering or treating of fabrics and textiles in aqueous washing, rinsing, or treating solutions formed from effective amounts of any of the detergent compositions, fabric softener compositions, or aqueous solution treatments described herein, or formed from the individual components of such compositions. Laundering of fabrics and textiles in such washing, rinsing and/or treatment solutions, followed by drying, imparts fabric appearance benefits to the fabric and textile articles so treated. Such benefits can include improved overall appearance, pill/fuzz reduction, anti-fading, improved abrasion resistance, and/or enhanced softness. It has been surprisingly determined that the dye maintenance polymers of this invention impart fabric appearance and integrity benefits that are greater than the benefits achieved by a corresponding amount of either component by itself.
These and other objects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. All percentages, ratios and proportions herein are by weight, unless otherwise specified.
All temperatures are in degrees Celsius (° C) unless otherwise specified.
DETAILED DESCRIPTION OF THE INVENTION
As noted, when fabric or textiles are laundered in solutions which comprise the dye maintenance polymers of the present invention fabric appearance and integrity are enhanced. The dye maintenance polymers can be added to wash solutions by incorporating them into a detergent composition, a fabric softener or by adding them separately to the washing solution. The dye maintenance polymers are described herein primarily as liquid or granular detergent additives but the present invention is not meant to be so limited. The dye maintenance polymers, detergent composition components, optional ingredients for such compositions and methods of using such compositions, are described in detail below. All percentages are by weight unless other specified.
Dve Maintenance Polymers Compositions and systems of the present invention comprise from about 0.1 %, preferably for about 1%, more preferably from about 2%, most preferably from about 3% to about 10%, preferably to about 7%, more preferably to about 5% by weight, of a polymer, co-polymer, or mixture thereof, wherein said polymer or co-polymer comprises at least one cationically charged unit, inter alia, quaternary ammonium moiety or unit which can form a cationic charge in situ, inter alia, primary amine moiety. Stated in another way, the oligomer, polymer, or co-polymer resulting from the herein below described monomer units must have a net cationic charge. The charge can be distributed among any of the herein described units.
The dye maintenance polymers of this invention can be used in any fabric laundering process and provide certain appearance benefits to the fabrics laundered in these processes. Such fabric appearance benefits can include, for example, improved overall appearance of the laundered fabrics, reduction of the formation of pills and fuzz, protection against color fading, improved abrasion resistance, etc. The dye maintenance polymers used in the compositions and methods herein can provide such fabric appearance benefits when incorporated in a wash or rinse added products.
As will be apparent to those skilled in the art, an oligomer is a molecule consisting of only a few monomer units while polymers comprise considerably more monomer units. For the present invention, oligomers are defined as molecules having an average molecular weight below about 1,000 and polymers are molecules having an average molecular weight of greater than about 1,000. Copolymers are polymers or oligomers wherein two or more dissimilar monomers have been simultaneously or sequentially polymerized. Copolymers of the present invention can include, for example, polymers or oligomers copolymerizing acrylamide with dimethyldiallylammonium chloride, vinyl amine with vinyl alcohol, etc Cationic polymers in general and their method of manufacture are know. For example, a detailed description of cationic polymers can be found in an article by M.
Fred Hoover that was published in the Journal ofMacromolecular Science-Chemistry, A4(6), pp 1327-1417, October, 1970. The dye maintenance polymers of this invention will be better understood when read in light of the Hoover article, the present disclosure and the Examples herein.
Linear Polymer Units The polymers or co-polymers of the present invention can comprise one or more linear polymer units having the formula:
C-C
RI Z
wherein R', RZ, and Z are defined herein below. Preferably, the linear polymer units are formed from linearly polymerizing monomers. Linearly polymerizing monomers are defined herein as monomers which under standard polymerizing conditions result in a linear polymer chain or alternatively which linearly propagate polymerization. The linearly polymerizing monomers of the present invention have the formula:
\C=C~
Rl~ Z .
however, those of skill in the art recognize that many useful linear monomer units are introduced indirectly, inter alia, vinyl amine units, vinyl alcohol units, and not by way of linearly polymerizing monomers. For example, vinyl acetate monomers once incorporated into the backbone are hydrolyzed to form vinyl alcohol units. For the purposes of the present invention, linear polymer units may be directly introduced, i.e. via linearly polymerizing units, or indirectly, i.e. via a precursor as in the case of vinyl alcohol cited herein above.
Each R' is independently hydrogen, C,-C4 alkyl, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic, and mixtures thereof. Preferably R' is hydrogen, C,-CQ alkyl, phenyl, and mixtures thereof, more preferably hydrogen and methyl.
Each RZ is independently hydrogen, halogen, C,-C4 alkyl, C,-C4 alkoxy, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic, and mixtures thereof. Preferred Rz is hydrogen, C,-CQ alkyl, and mixtures thereof.
Each Z is independently hydrogen; hydroxyl; halogen; -(CHZ)mR, wherein R is hydrogen, hydroxyl, halogen, nitrilo, -OR3, -O(CHZ)"N(R3)2, -O(CHZ)"N+(R3)3X-, -OCO(CHZ)~N(R3)z, OCO(CHZ)nN+(R3)3X , -NHCO(CHZ)"N(R3)z, -NHCO(CHZ)~N+(R3)3X , -(CHZ)"N(R3)2, -(CHZ)~N+(R3)3X-, a non-aromatic nitrogen heterocycle comprising a quaternary ammonium ion, a non-aromatic nitrogen heterocycle comprising an N-oxide moiety, an aromatic nitrogen containing heterocyclic wherein one or more or the nitrogen atoms is quaternized; an aromatic nitrogen containing heterocycle wherein at least one nitrogen is an N-oxide; -NHCHO
(formamide), -or mixtures thereof; wherein each R3 is independently hydrogen, C,-C8 alkyl, C,-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6;
carbocyclic, heterocyclic, or mixtures thereof; -(CHZ)mCOR' wherein R' is -OR3, -O(CHz)nN(R3)z, -O(CHz)nN+(R3)sX ~ -~3(CHz)~N(R3)z~ -~3(CHz)nN+(R3)sX ~ -(CHZ)nN(R3)2~ -(CHz)aN+(R3)sX
or mixtures thereof, wherein R3, X, and n are the same as defined herein above. A preferred Z is -O(CHZ)nN+(R3)3X-, wherein the index n is 2 to 4. The index m is from 0 to 6, preferably 0 to 2, more preferably 0.
Non-limiting examples of linearly polymerizing monomers comprising a heterocyclic Z
unit includes 1-vinyl-2-pyrrolidinone, 1-vinylimidazole, 2-vinyl-1,3-dioxolane, 4-vinyl-1-cyclohexenel,2-epoxide, and 2-vinylpyridine.
The polymers and co-polymers of the present invention comprise Z units which have a cationic charge or which result in a unit which forms a cationic charge in situ. When the co-polymers of the present invention comprise more than one Z unit, for example, Z', ZZ,...Z° units, at least about 1 % of the monomers which comprise the co-polymers will comprise a cationic unit.
Preferred cationic units include -O(CHZ)"N+(R3)3X- and -(CHZ)oN+(R3)3X-. When the co-polymers of the present invention are formed from two monomers, Z' and ZZ, the ratio of Z' to ZZ
is preferably from about 9:1 to about 1:9.
A non-limiting example of a Z unit which can be made to form a cationic charge in situ is the -NHCHO unit, formamide. The formulator can prepare a polymer or co-polymer comprising formamide units some of which are subsequently hydrolyzed to form vinyl amine equivalents.
For example the formulator may prepare a co-polymer having the general formula:
which comprises a formamide unit and then subsequently treat the co-polymer such that some of the formamide units are hydrolyzed to form a co-polymer comprising vinyl amine units, said polymer having the formula:
wherein Z may be a cationic unit comprising or non-cationic unit comprising moiety and x' + x" _ x.
Another class of preferred linearly polymerizable monomers comprise canonically charged heteroaromatic Z units having the formula:
/C=C
R
N+
R
an non-limiting example of which is 4-vinyl (N-alkyl)pyridine wherein R' and RZ are each hydrogen and R6 is methyl.
Another class of preferred linearly polymerizable monomers which comprises a heterocyclic ring includes Z units comprising an N-oxide, for example, the N-oxide having the formula:
R' RZ
\C=C~
R~~
N/
~O
a non-limiting example of which is 4-vinyl pyridine N-oxide.
N-alkyl vinylpyridine monomers and N-oxide vinylpyridine monomers can be suitably combined with other non aromatic monomers, inter alia, vinyl amine. However, preferred polymers of the present invention include co-polymers derived from a combination of quaternized, N-oxide, and nitrogen containing heteroaromatic monomers, non-limiting examples of which includes a copolymer of N-methyl vinyl pyridine and vinyl pyridine in a ratio of 4: l; a copolymer of N-methyl vinyl pyridine and vinyl pyridine in a ratio of 4:6; a co-polymer of poly(N-methyl vinyl pyridine) and vinyl pyridine N-oxide in a ratio of polymer to monomer of 4:1; poly(N-methyl vinyl pyridine) and vinyl pyridine N-oxide in a ratio of polymer to monomer of 4:6; and mixtures thereof.
A preferred linear co-polymer according to the present has the formula:
Z~ Jx ~ ZZ J y wherein Z' has the formula:
O NH2.
Z2 has the formula:
~H3 X_ N+_ O O~ ~ CH3 wherein X is chlorine; x has the value of from about 10 to about 100,000; y has the value of from about 10 to about 100,000; the ratio of x to y is from 9:1 to 1:9. Co-polymers of this type are available as, e.g., Sedipur~ CF104 ex BASF.
As described herein above, some preferred polymer residues may be formed by treatment of the resulting polymer. For example, vinyl amine residues are preferably introduced via formamide monomers which are subsequently hydrolyzed to the free amino unit. Also vinyl alcohol units are obtained by hydrolysis of residues formed form vinyl acetate monomers.
Likewise, acrylic acid residues may be esterified after polymerization, for example, units having the formula:
N+_ O O~ ~ CH3 may be more conveniently formed after the backbone has been formed by polymerization with acrylic acid or acrylic acid precursor monomers.
II) Cyclic Units Derived from Cyclically Polymerizing Monomers The polymers or co-polymers of the present invention can comprise one or more cyclic polymer units which are derived from cyclically polymerizing monomers.
Cyclically polymerizing monomers are defined herein as monomers which under standard polymerizing conditions result in a cyclic polymer residue as well as serving to linearly propagate polymerization. Preferred cyclically polymerizing monomers of the present invention have the formula:
Ra _ X
Ra-N~ Rs Rs wherein each R4 is independently an olefin comprising unit which is capable of propagating polymerization in addition to forming a cyclic residue with an adjacent R4 unit; RS is C,-C,2 linear or branched alkyl, benzyl, substituted benzyl, and mixtures thereof; X is a water soluble anion.
Non-limiting examples of R4 units include allyl and alkyl substituted allyl units.
Preferably the resulting cyclic residue is a six-member ring comprising a quaternary nitrogen atom.
RS is preferably C,-C4 alkyl, preferably methyl.
An example of a cyclically polymerizing monomer is dimethyl diallyl ammonium having the formula:
N+
/\
which results in a polymer or co-polymer having units with the formula:
N+ X-z wherein preferably the index z is from about 10 to about 50,000.
III) Mixtures thereof.
The polymers or co-polymers of the present invention must retain a net cationic charge, whether the charged is developed in situ, or whether the polymer or co-polymer itself has a formal positive charge. Preferably the polymer or co-polymer has at least 10%, more preferably at least about 25%, more preferably at least about 35%, most preferably at least about 50% of the residues comprise a cationic charge.
The polymers or co-polymers of the present invention can comprise mixtures of linearly and cyclically polymerizing monomers, for example the poly(dimethyldiallyl-ammonium chloride/acrylamide) co-polymer having the formula:
wherein Z', Z2, x, y, and z are the same as defined herein above and X is chloride ion.
A particularly preferred embodiment of this invention is the composition comprising a polymer based on dimethyldiallylammonium chloride and a copolymer which is based upon acrylamide with a co-monomer selected from the group consisting of N, N
dialkylaminoalkyl(meth)acrylate, N, N dialkylaminoalkylacrylate, N,N
dialkylaminoalkylacrylamide, N,N dialkylaminoalkyl(meth)acrylamide, their quaternized derivatives and mixtures thereof.
Non-limiting examples of preferred polymers according to the present invention include dye maintenance copolymers comprising:
i) a first monomer selected from the group consisting of N, N
dialkylaminoalkyl(meth)acrylate, N, N dialkylaminoalkylacrylate, N,N
dialkylaminoalkylacrylamide, N,N dialkylaminoalkyl(meth)acrylamide, their quaternized derivatives and mixtures thereof; and ii) a second monomer selected from the group consisting of acrylic acid, methacrylic acid, C,-C6 alkylmethacrylate, C,-C6 alkyl acrylate, C,-C8 hydroxyalkylacrylate, C,-C8 hydroxyalkylmethacrylate, acrylamide, C,-C,6 alkyl acrylamide, C,-C,6 dialkylacrylamide, 2-acrylamido-2-methylpropane sulfonic acid or its alkali salt, methacrylamide, C,-C,6 alkylmethacrylamide, C,-C,6 dialkylmethacrylamide, vinyl formamide, vinylacetamide, vinyl alcohol, C,-C8 vinylalkylether, vinyl pyridine, itaconic acid, vinyl acetate, vinyl propionate, vinyl butyrate and mixtures thereof;
wherein the copolymer comprises at least 25 mole % of the first monomer.
ADJUNCT INGREDIENTS
The compositions of the present invention may also optionally comprise one or more adjunct ingredients. Non-limiting examples of adjunct ingredients are selected from the group consisting of detersive surfactants, electrolytes, stabilizers, low molecular weight water soluble solvents, chelating agents, dispersibility aids, soil release agents, nonionic fabric softening agents, concentration aid, perfume, preservatives, colorants, optical brighteners, opacifiers, germicides, fungicides, anti-corrosion agents, antifoam agents, and mixtures thereof.
The following are applications which describe various detergent additive, methods of making these additives and methods of using them. WO 99/07813 A 1 Randall et al., "Laundry Detergent Compositions with Amino Acid Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO 99/07814 Randall et al., "Laundry Detergent Compositions with Amino Acid Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO
Panandiker et al., "Laundry Detergent Compositions with Anionically Modified, Cyclic Amine Based Polymers; WO 99/14300 A1 Panandiker et al., "Laundry Detergent Compositions with Cyclic Amine-Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO 99/14301 A1 Panandiker et al., "Laundry Detergent Compositions and Fabric Conditioning Compositions with Oxidized Cyclic Amine-Based Polymers"; and WO 00/22078 Panandiker et al., "Laundry Detergent Compositions with A
Combination of Cyclic Amine Based Polymers and Hydrophobically Modified Carboxy Methyl Cellulose".
SURFACTANT SYSTEM
The laundry detergent compositions of the present invention comprise a surfactant system. The surfactant systems of the present invention may comprise any type of detersive surfactant, non-limiting examples of which include one or more mid-chain branched alkyl sulfate surfactants, one or more mid-chain branched alkyl aIkoxy sulfate surfactants, one or more mid-chain branched aryl sulfonate surfactants, one or more non mid-chain branched sulphonates, sulphates, cationic surfactants, zwitterionic surfactants, ampholytic surfactants, and mixtures thereof.
The total amount of surfactant present in the compositions of the present invention is from about 4% by weight, preferably from about 10% more preferably from about 15% to about 60%, preferably to about 30% by weight, of said composition.
Nonlimiting examples of surfactants useful herein include:
a) C"-C,8 alkyl benzene sulfonates (LAS);
b) C6-C,8 mid-chain branched aryl sulfonates (BLAS);
c) C,°-CZO primary, a or cc~-branched, and random alkyl sulfates (AS);
d) C"-C~ mid-chain branched alkyl sulfates (BAS);
e) C,°-C,e secondary (2,3) alkyl sulfates as described in U.S.
3,234,258 Morris, issued February 8, 1966; U.S. 5,075,041 Lutz, issued December 24, 1991; U.S.
5,349,101 Lutz is et al., issued September 20, 1994; and U.S. 5,389,277 Prieto, issued February 14, 1995;
f) C,o-C,8 alkyl alkoxy sulfates (AExS) wherein preferably x is from 1-7;
g) C"-C~ mid-chain branched alkyl alkoxy sulfates (BAE,S);
h) C,o-C,e alkyl alkoxy carboxylates preferably comprising 1-5 ethoxy units;
i) C,2-C,e alkyl.ethoxylabes, C6-C,i alkyl phenol alkoxylates wherein the alkoxylate units are a mixture of ethyleneoxy and propyltneoxy units, C,2-C,e alcohol and C6-C,z alkyl phenol condensates with ethylene oxide/propylene oxide block polymers inter alia Pluronic~ ex BASF which are disclosed in U.S. 3,929,678 Laughlin et al., issued December 30, 1975;
j) C"-CZZ mid-chain branched alkyl alkoxylates, BAEx;
k) Alkylpolysaccharides as disclosed in U.S. 4;565,647 Llenado, issued January 26, 1986;
1) Polyhydroxy fatty acid' amides having the formula:
R~ C-N-Q
wherein R' is CS-C3, alkyl; R$ is selected from the group consisting of hydrogen, C,-C, alkyl, C,-C~ hydroxyalkyl, Q is a polyhydroxyalkyl moiety having a linear alkyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof; prefen ed alkoxy is ethoxy or propoxy, and mixtures thereof; prefer ed Q is derived from a reducing sugar in a reductive amination reaction, more preferably Q is a glycityl moiety; Q is more preferably selected from the group consisting of -CHZ(CHOH)"CHZOH, -CH(CHZOH)(CHOH)".,CH,OH, -CHZ(CHOH)Z(CHOR')(CHOH) CHZ OH, and alkoxylated derivatives thereof, wherein n is an integer from 3 to 5, inclusive, and R' is hydrogen or a cyclic or aliphatic monosaccharide, which are described in U.S. 5,489,393 Connor et al., issued February 6, 1996; and U.S. 5,45,982 Murch et al., issued October 3, 1995.
A non-limiting example of a nonionic surfactant suitable for use in the present invention has the formula:
O
R-C-N-((R~O)x(RZO)yR3)m ~~n wherein R is C,-C~, linear alkyl, C,-Ci, branched alkyl, CT-CZ, linear alkenyl, C,-CZ, branched alkenyl, and mixtures thereof.
R' is ethylene; RZis C3-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof;
preferably RZ is 1,2-propylene. Nonionic surfactants which comprise a mixture of R' and RZUnits preferably comprise from about 4 to about 12 ethylene units in combination with from about 1 to about 4 1,2-propylene units. The units may be alternating, or grouped together in any combination suitable to the formulator. Preferably the ratio of R' units to RZ
units is from about 4 1 to about 8 : 1. Preferably an RZ units (i.e. 1,2-propylene) is attached to the nitrogen atom followed by the balance of the chain comprising from 4 to 8 ethylene units.
R2 is hydrogen, C,-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof; preferably hydrogen or methyl, more preferably hydrogen.
R4 is hydrogen, C,-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof; preferably hydrogen. When the index m is equal to 2 the index n must be equal to 0 and the R' unit is absent and is instead replaced by a -[(R'O)X(RZO)yR3] unit.
The index m is 1 or 2, the index n is 0 or 1, provided that when m is equal to 1, n is equal to 1; and when m is 2 n is 0; preferably m is equal to 1 and n is equal to one, resulting in one -[(R'O)X(RZO)S.R3] unit and R4 being present on the nitrogen. The index x is from 0 to about 50, preferably from about 3 to about 25, more preferably from about 3 to about 10.
The index y is from 0 to about 10, preferably 0, however when the index y is not equal to 0, y is from 1 to about 4. Preferably all of the alkyleneoxy units are ethyleneoxy units. Those skilled in the art of ethoxylated polyoxyalkylene alkyl amide surface active agents will recognized that the values for the indices x and y are average values and the true values may range over several values depending upon the process used to alkoxylate the amides.
The mid-chain branched alkyl sulfate surfactants of the present invention have the formula:
DYE MAINTENANCE POLYMERS
FIELD OF THE INVENTION
The present invention relates to compositions, in either liquid or granular form, for use in laundry applications, wherein the compositions comprise certain dye maintenance polymers that have a net positive charge. Compositions comprising the dye maintenance polymers of this invention impart appearance and integrity benefits to fabrics and textiles laundered in washing solutions formed from such compositions.
BACKGROUND OF THE INVENTION
It is, of course, well lrnown that alternating cycles of using and laundering fabrics and textiles, such as articles of worn clothing and apparel, will inevitably adversely affect the appearance and integrity of the fabric and textile items so used and laundered. Fabrics and textiles simply wear out over time and with use. Laundering of fabrics and textiles is necessary to remove soils and stains which accumulate therein and thereon during ordinary use. However, the laundering operation itself, over many cycles, can accentuate and contribute to the deterioration of the integrity and the appearance of such fabrics and textiles.
Deterioration of fabric integrity and appearance can manifest itself in several ways. Short fibers are dislodged from woven and lrnit fabric/textile structures by the mechanical action of laundering. These dislodged fibers may form lint, fuzz or "pills" which are visible on the surface of fabrics and diminish the appearance of newness of the fabric. Further, repeated laundering of fabrics and textiles, especially with bleach-containing laundry products, can remove dye from fabrics and textiles and impart a faded, worn out appearance as a result of diminished color intensity, and in many cases, as a result of changes in hues or shades of color.
Given the foregoing, there is clearly an ongoing need to identify materials which could be added to laundry products that would associate themselves with the fibers of the fabrics and textiles laundered using such products and thereby reduce or minimize the tendency of the laundered fabric/textiles to deteriorate in appearance. Any such detergent product additive material should, of course, be able to benefit fabric appearance and integrity without unduly interfering with the ability of the laundry product to perform its intended function. The present invention is directed to the use of dye maintenance polymers in laundry applications that perform in this desired manner.
SUMMARY OF TIC INVENTION
The present invention meets the aforementioned need in that it has been surprisingly discovered that fabric which is treated, and subsequently re-treated with the compositions of the present invention, will resist normal fading and color loss without regard to the circumstances, inter alia, due to mechanical wear and abrasion. In addition, fabric which has not been treated can have the loss of fabric dye attenuated by washing clothing with the laundry detergent compositions of the present invention. The compositions of the present invention can take any form, inter alia, heavy duty liquid (HDL), heavy duty granular (HDG), bars, pastes, thixotropic compositions.
In one embodiment the present invention provides a detergent composition comprising:
a) from 4% to 70% by weight, of a surfactant; b) from 0.01 % to 10% by weight, of a dye maintenance co-polymer, said copolymer having the general formula:
A
x has the value of from 10 to 100,000; y has the value of from 10 to 100,000;
the ratio of x to y is from 9:1 to 1:9; each Z is independently (CH2)mCOR' wherein R' is selected from: i) -OR3;
ii) -O(CHz)°N(R3h; iii) -0(CHz)r,N+(R3)3X ; iv) -NR3(CHZ)°N(R3~;
v) -NR3(CHZ~,N+(R3~X ;
vi) -(CHz)"N(R3)Z; vii) -(CHZ)"N+(R3)3X-; viii) or mixtures thereof; each R3 is independently hydrogen, Cl-Cg alkyl, CZ-C$ hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6; the index m is from 0 to 6; provided said co-polymer has a net cationic charge; and wherein said dye maintenance co-polymer is not an polyethyleneimine or alkoxylated derivative thereof; and c) the balance carriers and other adjunct ingredients.
Another aspect of the present invention relates to laundry detergent compositions providing dye protection benefits to fabric comprising:
2a a) from about 4% to about 70% by weight, of a surfactant selected from the group consisting of nonionic, anionic, cationic, amphoteric, zwitterionic surfactants and mixtures thereof, preferably at least one of said surfactants is an anionic surfactant;
b) from about 0.01 %, preferably from about 0.1 %, more preferably from about 0.5%, most preferably from about 0.8% to about 10%, preferably to about 8%, more preferably to about 6%, most preferably to about 5% by weight, of a dye maintenance polymer or oligomer, said polymer or copolymer comprising one or more units having the formula:
I) linear polymer units having the formula:
R~ R2 I ~
C-C
R~ Z
wherein each R' is independently a) hydrogen;
b) C1-C4 alkyl;
c) substituted or unsubstituted phenyl;
d) substituted or unsubstituted benzyl;
e) carbocyclic;
f) heterocyclic;
g) and mixtures thereof;
eachRZ is independently a) hydrogen;
b) halogen c) C,-C4 alkyl;
d) C,-C4 alkoxy;
e) substituted or unsubstituted phenyl;
f) substituted or unsubstituted benzyl;
g) carbocyclic;
h) heterocyclic;
i) and mixtures thereof;
eachZ is independently a) hydrogen;
b) hydroxyl;
c) halogen;
d) -(CHZ),"R;
wherein R is:
i) hydrogen;
ii) hydroxyl iii) halogen;
iv) nitrilo;
v) -OR3;
vi) -O(CHZ)"N(R3)Z;
vii) -O(CHZ)"N+(R3)3X
;
viii) -OCO(CHZ)"N(R3)z;
ix) -OCO(CHZ)"N+(R3)3X
-;
x) -NHCO(CHZ)"N(R3)2;
xi) -NHCO(CHZ)"N+(R3)3X-;
xii) -(CHZ)"N(R3)z;
xiii) -(CHz)oN+(R3)sX ;
xiv) carbocyclic;
xv) heterocyclic;
xvi) nitrogen heterocycle quaternary ammonium;
xvii) nitrogen heterocycle N-oxide;
xviii) aromatic N-heterocyclic quaternary ammonium;
xix) aromatic N-heterocyclic N-oxide;
xx) -NHCHO;
xxi) or mixtures thereof;
each R3 is independently hydrogen, C,-Cg alkyl, CZ-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion;
the index n is from 0 to 6 e) -(CHZ)",COR' wherein R' is i) -OR3;
ii) -O(CHZ)nN(R3)2;
iii) -O(CHz)"N+(R3)sX
-;
iv) -NR3(CHZ)"N(R3)z;
-NR3(CHz)nN+(R3)sX
v1) -(CHZ)nN(R3)2i v11) -(CHZ)nN+(R3)sX
, viii) or mixtures thereof;
each R3 is independently hydrogen, C,-Cg alkyl, CZ-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion;
the index n is from 0 to 6;
f) and mixtures thereof;
the index m is from 0 to 6;
II) cyclic units derived from cyclically polymerizing monomers having the formula:
Ra _ X
Ra-N~ Rs Rs wherein each R4 is independently an olefin comprising unit which is capable of propagating polymerization in addition to forming a cyclic residue with an adjacent R4 unit; RS is C,-C,2 linear or branched alkyl, benzyl, substituted benzyl, and mixtures thereof; X is a water soluble anion; and III) mixtures thereof;
provided said polymer or co-polymer has a net cationic charge; and wherein said dye maintenance polymer is not an polyethyleneimine or alkoxylated derivative thereof; and b) the balance carriers and other adjunct ingredients.
In addition to the surfactant and the dye maintenance polymer of this invention, the laundry detergent compositions herein comprise from about 0.01% to 80% by weight of an organic or inorganic detergency builder and other conventional laundry detergent products.
In its method aspect, the present invention relates to the laundering or treating of fabrics and textiles in aqueous washing, rinsing, or treating solutions formed from effective amounts of any of the detergent compositions, fabric softener compositions, or aqueous solution treatments described herein, or formed from the individual components of such compositions. Laundering of fabrics and textiles in such washing, rinsing and/or treatment solutions, followed by drying, imparts fabric appearance benefits to the fabric and textile articles so treated. Such benefits can include improved overall appearance, pill/fuzz reduction, anti-fading, improved abrasion resistance, and/or enhanced softness. It has been surprisingly determined that the dye maintenance polymers of this invention impart fabric appearance and integrity benefits that are greater than the benefits achieved by a corresponding amount of either component by itself.
These and other objects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. All percentages, ratios and proportions herein are by weight, unless otherwise specified.
All temperatures are in degrees Celsius (° C) unless otherwise specified.
DETAILED DESCRIPTION OF THE INVENTION
As noted, when fabric or textiles are laundered in solutions which comprise the dye maintenance polymers of the present invention fabric appearance and integrity are enhanced. The dye maintenance polymers can be added to wash solutions by incorporating them into a detergent composition, a fabric softener or by adding them separately to the washing solution. The dye maintenance polymers are described herein primarily as liquid or granular detergent additives but the present invention is not meant to be so limited. The dye maintenance polymers, detergent composition components, optional ingredients for such compositions and methods of using such compositions, are described in detail below. All percentages are by weight unless other specified.
Dve Maintenance Polymers Compositions and systems of the present invention comprise from about 0.1 %, preferably for about 1%, more preferably from about 2%, most preferably from about 3% to about 10%, preferably to about 7%, more preferably to about 5% by weight, of a polymer, co-polymer, or mixture thereof, wherein said polymer or co-polymer comprises at least one cationically charged unit, inter alia, quaternary ammonium moiety or unit which can form a cationic charge in situ, inter alia, primary amine moiety. Stated in another way, the oligomer, polymer, or co-polymer resulting from the herein below described monomer units must have a net cationic charge. The charge can be distributed among any of the herein described units.
The dye maintenance polymers of this invention can be used in any fabric laundering process and provide certain appearance benefits to the fabrics laundered in these processes. Such fabric appearance benefits can include, for example, improved overall appearance of the laundered fabrics, reduction of the formation of pills and fuzz, protection against color fading, improved abrasion resistance, etc. The dye maintenance polymers used in the compositions and methods herein can provide such fabric appearance benefits when incorporated in a wash or rinse added products.
As will be apparent to those skilled in the art, an oligomer is a molecule consisting of only a few monomer units while polymers comprise considerably more monomer units. For the present invention, oligomers are defined as molecules having an average molecular weight below about 1,000 and polymers are molecules having an average molecular weight of greater than about 1,000. Copolymers are polymers or oligomers wherein two or more dissimilar monomers have been simultaneously or sequentially polymerized. Copolymers of the present invention can include, for example, polymers or oligomers copolymerizing acrylamide with dimethyldiallylammonium chloride, vinyl amine with vinyl alcohol, etc Cationic polymers in general and their method of manufacture are know. For example, a detailed description of cationic polymers can be found in an article by M.
Fred Hoover that was published in the Journal ofMacromolecular Science-Chemistry, A4(6), pp 1327-1417, October, 1970. The dye maintenance polymers of this invention will be better understood when read in light of the Hoover article, the present disclosure and the Examples herein.
Linear Polymer Units The polymers or co-polymers of the present invention can comprise one or more linear polymer units having the formula:
C-C
RI Z
wherein R', RZ, and Z are defined herein below. Preferably, the linear polymer units are formed from linearly polymerizing monomers. Linearly polymerizing monomers are defined herein as monomers which under standard polymerizing conditions result in a linear polymer chain or alternatively which linearly propagate polymerization. The linearly polymerizing monomers of the present invention have the formula:
\C=C~
Rl~ Z .
however, those of skill in the art recognize that many useful linear monomer units are introduced indirectly, inter alia, vinyl amine units, vinyl alcohol units, and not by way of linearly polymerizing monomers. For example, vinyl acetate monomers once incorporated into the backbone are hydrolyzed to form vinyl alcohol units. For the purposes of the present invention, linear polymer units may be directly introduced, i.e. via linearly polymerizing units, or indirectly, i.e. via a precursor as in the case of vinyl alcohol cited herein above.
Each R' is independently hydrogen, C,-C4 alkyl, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic, and mixtures thereof. Preferably R' is hydrogen, C,-CQ alkyl, phenyl, and mixtures thereof, more preferably hydrogen and methyl.
Each RZ is independently hydrogen, halogen, C,-C4 alkyl, C,-C4 alkoxy, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic, and mixtures thereof. Preferred Rz is hydrogen, C,-CQ alkyl, and mixtures thereof.
Each Z is independently hydrogen; hydroxyl; halogen; -(CHZ)mR, wherein R is hydrogen, hydroxyl, halogen, nitrilo, -OR3, -O(CHZ)"N(R3)2, -O(CHZ)"N+(R3)3X-, -OCO(CHZ)~N(R3)z, OCO(CHZ)nN+(R3)3X , -NHCO(CHZ)"N(R3)z, -NHCO(CHZ)~N+(R3)3X , -(CHZ)"N(R3)2, -(CHZ)~N+(R3)3X-, a non-aromatic nitrogen heterocycle comprising a quaternary ammonium ion, a non-aromatic nitrogen heterocycle comprising an N-oxide moiety, an aromatic nitrogen containing heterocyclic wherein one or more or the nitrogen atoms is quaternized; an aromatic nitrogen containing heterocycle wherein at least one nitrogen is an N-oxide; -NHCHO
(formamide), -or mixtures thereof; wherein each R3 is independently hydrogen, C,-C8 alkyl, C,-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6;
carbocyclic, heterocyclic, or mixtures thereof; -(CHZ)mCOR' wherein R' is -OR3, -O(CHz)nN(R3)z, -O(CHz)nN+(R3)sX ~ -~3(CHz)~N(R3)z~ -~3(CHz)nN+(R3)sX ~ -(CHZ)nN(R3)2~ -(CHz)aN+(R3)sX
or mixtures thereof, wherein R3, X, and n are the same as defined herein above. A preferred Z is -O(CHZ)nN+(R3)3X-, wherein the index n is 2 to 4. The index m is from 0 to 6, preferably 0 to 2, more preferably 0.
Non-limiting examples of linearly polymerizing monomers comprising a heterocyclic Z
unit includes 1-vinyl-2-pyrrolidinone, 1-vinylimidazole, 2-vinyl-1,3-dioxolane, 4-vinyl-1-cyclohexenel,2-epoxide, and 2-vinylpyridine.
The polymers and co-polymers of the present invention comprise Z units which have a cationic charge or which result in a unit which forms a cationic charge in situ. When the co-polymers of the present invention comprise more than one Z unit, for example, Z', ZZ,...Z° units, at least about 1 % of the monomers which comprise the co-polymers will comprise a cationic unit.
Preferred cationic units include -O(CHZ)"N+(R3)3X- and -(CHZ)oN+(R3)3X-. When the co-polymers of the present invention are formed from two monomers, Z' and ZZ, the ratio of Z' to ZZ
is preferably from about 9:1 to about 1:9.
A non-limiting example of a Z unit which can be made to form a cationic charge in situ is the -NHCHO unit, formamide. The formulator can prepare a polymer or co-polymer comprising formamide units some of which are subsequently hydrolyzed to form vinyl amine equivalents.
For example the formulator may prepare a co-polymer having the general formula:
which comprises a formamide unit and then subsequently treat the co-polymer such that some of the formamide units are hydrolyzed to form a co-polymer comprising vinyl amine units, said polymer having the formula:
wherein Z may be a cationic unit comprising or non-cationic unit comprising moiety and x' + x" _ x.
Another class of preferred linearly polymerizable monomers comprise canonically charged heteroaromatic Z units having the formula:
/C=C
R
N+
R
an non-limiting example of which is 4-vinyl (N-alkyl)pyridine wherein R' and RZ are each hydrogen and R6 is methyl.
Another class of preferred linearly polymerizable monomers which comprises a heterocyclic ring includes Z units comprising an N-oxide, for example, the N-oxide having the formula:
R' RZ
\C=C~
R~~
N/
~O
a non-limiting example of which is 4-vinyl pyridine N-oxide.
N-alkyl vinylpyridine monomers and N-oxide vinylpyridine monomers can be suitably combined with other non aromatic monomers, inter alia, vinyl amine. However, preferred polymers of the present invention include co-polymers derived from a combination of quaternized, N-oxide, and nitrogen containing heteroaromatic monomers, non-limiting examples of which includes a copolymer of N-methyl vinyl pyridine and vinyl pyridine in a ratio of 4: l; a copolymer of N-methyl vinyl pyridine and vinyl pyridine in a ratio of 4:6; a co-polymer of poly(N-methyl vinyl pyridine) and vinyl pyridine N-oxide in a ratio of polymer to monomer of 4:1; poly(N-methyl vinyl pyridine) and vinyl pyridine N-oxide in a ratio of polymer to monomer of 4:6; and mixtures thereof.
A preferred linear co-polymer according to the present has the formula:
Z~ Jx ~ ZZ J y wherein Z' has the formula:
O NH2.
Z2 has the formula:
~H3 X_ N+_ O O~ ~ CH3 wherein X is chlorine; x has the value of from about 10 to about 100,000; y has the value of from about 10 to about 100,000; the ratio of x to y is from 9:1 to 1:9. Co-polymers of this type are available as, e.g., Sedipur~ CF104 ex BASF.
As described herein above, some preferred polymer residues may be formed by treatment of the resulting polymer. For example, vinyl amine residues are preferably introduced via formamide monomers which are subsequently hydrolyzed to the free amino unit. Also vinyl alcohol units are obtained by hydrolysis of residues formed form vinyl acetate monomers.
Likewise, acrylic acid residues may be esterified after polymerization, for example, units having the formula:
N+_ O O~ ~ CH3 may be more conveniently formed after the backbone has been formed by polymerization with acrylic acid or acrylic acid precursor monomers.
II) Cyclic Units Derived from Cyclically Polymerizing Monomers The polymers or co-polymers of the present invention can comprise one or more cyclic polymer units which are derived from cyclically polymerizing monomers.
Cyclically polymerizing monomers are defined herein as monomers which under standard polymerizing conditions result in a cyclic polymer residue as well as serving to linearly propagate polymerization. Preferred cyclically polymerizing monomers of the present invention have the formula:
Ra _ X
Ra-N~ Rs Rs wherein each R4 is independently an olefin comprising unit which is capable of propagating polymerization in addition to forming a cyclic residue with an adjacent R4 unit; RS is C,-C,2 linear or branched alkyl, benzyl, substituted benzyl, and mixtures thereof; X is a water soluble anion.
Non-limiting examples of R4 units include allyl and alkyl substituted allyl units.
Preferably the resulting cyclic residue is a six-member ring comprising a quaternary nitrogen atom.
RS is preferably C,-C4 alkyl, preferably methyl.
An example of a cyclically polymerizing monomer is dimethyl diallyl ammonium having the formula:
N+
/\
which results in a polymer or co-polymer having units with the formula:
N+ X-z wherein preferably the index z is from about 10 to about 50,000.
III) Mixtures thereof.
The polymers or co-polymers of the present invention must retain a net cationic charge, whether the charged is developed in situ, or whether the polymer or co-polymer itself has a formal positive charge. Preferably the polymer or co-polymer has at least 10%, more preferably at least about 25%, more preferably at least about 35%, most preferably at least about 50% of the residues comprise a cationic charge.
The polymers or co-polymers of the present invention can comprise mixtures of linearly and cyclically polymerizing monomers, for example the poly(dimethyldiallyl-ammonium chloride/acrylamide) co-polymer having the formula:
wherein Z', Z2, x, y, and z are the same as defined herein above and X is chloride ion.
A particularly preferred embodiment of this invention is the composition comprising a polymer based on dimethyldiallylammonium chloride and a copolymer which is based upon acrylamide with a co-monomer selected from the group consisting of N, N
dialkylaminoalkyl(meth)acrylate, N, N dialkylaminoalkylacrylate, N,N
dialkylaminoalkylacrylamide, N,N dialkylaminoalkyl(meth)acrylamide, their quaternized derivatives and mixtures thereof.
Non-limiting examples of preferred polymers according to the present invention include dye maintenance copolymers comprising:
i) a first monomer selected from the group consisting of N, N
dialkylaminoalkyl(meth)acrylate, N, N dialkylaminoalkylacrylate, N,N
dialkylaminoalkylacrylamide, N,N dialkylaminoalkyl(meth)acrylamide, their quaternized derivatives and mixtures thereof; and ii) a second monomer selected from the group consisting of acrylic acid, methacrylic acid, C,-C6 alkylmethacrylate, C,-C6 alkyl acrylate, C,-C8 hydroxyalkylacrylate, C,-C8 hydroxyalkylmethacrylate, acrylamide, C,-C,6 alkyl acrylamide, C,-C,6 dialkylacrylamide, 2-acrylamido-2-methylpropane sulfonic acid or its alkali salt, methacrylamide, C,-C,6 alkylmethacrylamide, C,-C,6 dialkylmethacrylamide, vinyl formamide, vinylacetamide, vinyl alcohol, C,-C8 vinylalkylether, vinyl pyridine, itaconic acid, vinyl acetate, vinyl propionate, vinyl butyrate and mixtures thereof;
wherein the copolymer comprises at least 25 mole % of the first monomer.
ADJUNCT INGREDIENTS
The compositions of the present invention may also optionally comprise one or more adjunct ingredients. Non-limiting examples of adjunct ingredients are selected from the group consisting of detersive surfactants, electrolytes, stabilizers, low molecular weight water soluble solvents, chelating agents, dispersibility aids, soil release agents, nonionic fabric softening agents, concentration aid, perfume, preservatives, colorants, optical brighteners, opacifiers, germicides, fungicides, anti-corrosion agents, antifoam agents, and mixtures thereof.
The following are applications which describe various detergent additive, methods of making these additives and methods of using them. WO 99/07813 A 1 Randall et al., "Laundry Detergent Compositions with Amino Acid Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO 99/07814 Randall et al., "Laundry Detergent Compositions with Amino Acid Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO
Panandiker et al., "Laundry Detergent Compositions with Anionically Modified, Cyclic Amine Based Polymers; WO 99/14300 A1 Panandiker et al., "Laundry Detergent Compositions with Cyclic Amine-Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO 99/14301 A1 Panandiker et al., "Laundry Detergent Compositions and Fabric Conditioning Compositions with Oxidized Cyclic Amine-Based Polymers"; and WO 00/22078 Panandiker et al., "Laundry Detergent Compositions with A
Combination of Cyclic Amine Based Polymers and Hydrophobically Modified Carboxy Methyl Cellulose".
SURFACTANT SYSTEM
The laundry detergent compositions of the present invention comprise a surfactant system. The surfactant systems of the present invention may comprise any type of detersive surfactant, non-limiting examples of which include one or more mid-chain branched alkyl sulfate surfactants, one or more mid-chain branched alkyl aIkoxy sulfate surfactants, one or more mid-chain branched aryl sulfonate surfactants, one or more non mid-chain branched sulphonates, sulphates, cationic surfactants, zwitterionic surfactants, ampholytic surfactants, and mixtures thereof.
The total amount of surfactant present in the compositions of the present invention is from about 4% by weight, preferably from about 10% more preferably from about 15% to about 60%, preferably to about 30% by weight, of said composition.
Nonlimiting examples of surfactants useful herein include:
a) C"-C,8 alkyl benzene sulfonates (LAS);
b) C6-C,8 mid-chain branched aryl sulfonates (BLAS);
c) C,°-CZO primary, a or cc~-branched, and random alkyl sulfates (AS);
d) C"-C~ mid-chain branched alkyl sulfates (BAS);
e) C,°-C,e secondary (2,3) alkyl sulfates as described in U.S.
3,234,258 Morris, issued February 8, 1966; U.S. 5,075,041 Lutz, issued December 24, 1991; U.S.
5,349,101 Lutz is et al., issued September 20, 1994; and U.S. 5,389,277 Prieto, issued February 14, 1995;
f) C,o-C,8 alkyl alkoxy sulfates (AExS) wherein preferably x is from 1-7;
g) C"-C~ mid-chain branched alkyl alkoxy sulfates (BAE,S);
h) C,o-C,e alkyl alkoxy carboxylates preferably comprising 1-5 ethoxy units;
i) C,2-C,e alkyl.ethoxylabes, C6-C,i alkyl phenol alkoxylates wherein the alkoxylate units are a mixture of ethyleneoxy and propyltneoxy units, C,2-C,e alcohol and C6-C,z alkyl phenol condensates with ethylene oxide/propylene oxide block polymers inter alia Pluronic~ ex BASF which are disclosed in U.S. 3,929,678 Laughlin et al., issued December 30, 1975;
j) C"-CZZ mid-chain branched alkyl alkoxylates, BAEx;
k) Alkylpolysaccharides as disclosed in U.S. 4;565,647 Llenado, issued January 26, 1986;
1) Polyhydroxy fatty acid' amides having the formula:
R~ C-N-Q
wherein R' is CS-C3, alkyl; R$ is selected from the group consisting of hydrogen, C,-C, alkyl, C,-C~ hydroxyalkyl, Q is a polyhydroxyalkyl moiety having a linear alkyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof; prefen ed alkoxy is ethoxy or propoxy, and mixtures thereof; prefer ed Q is derived from a reducing sugar in a reductive amination reaction, more preferably Q is a glycityl moiety; Q is more preferably selected from the group consisting of -CHZ(CHOH)"CHZOH, -CH(CHZOH)(CHOH)".,CH,OH, -CHZ(CHOH)Z(CHOR')(CHOH) CHZ OH, and alkoxylated derivatives thereof, wherein n is an integer from 3 to 5, inclusive, and R' is hydrogen or a cyclic or aliphatic monosaccharide, which are described in U.S. 5,489,393 Connor et al., issued February 6, 1996; and U.S. 5,45,982 Murch et al., issued October 3, 1995.
A non-limiting example of a nonionic surfactant suitable for use in the present invention has the formula:
O
R-C-N-((R~O)x(RZO)yR3)m ~~n wherein R is C,-C~, linear alkyl, C,-Ci, branched alkyl, CT-CZ, linear alkenyl, C,-CZ, branched alkenyl, and mixtures thereof.
R' is ethylene; RZis C3-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof;
preferably RZ is 1,2-propylene. Nonionic surfactants which comprise a mixture of R' and RZUnits preferably comprise from about 4 to about 12 ethylene units in combination with from about 1 to about 4 1,2-propylene units. The units may be alternating, or grouped together in any combination suitable to the formulator. Preferably the ratio of R' units to RZ
units is from about 4 1 to about 8 : 1. Preferably an RZ units (i.e. 1,2-propylene) is attached to the nitrogen atom followed by the balance of the chain comprising from 4 to 8 ethylene units.
R2 is hydrogen, C,-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof; preferably hydrogen or methyl, more preferably hydrogen.
R4 is hydrogen, C,-C4 linear alkyl, C3-C4 branched alkyl, and mixtures thereof; preferably hydrogen. When the index m is equal to 2 the index n must be equal to 0 and the R' unit is absent and is instead replaced by a -[(R'O)X(RZO)yR3] unit.
The index m is 1 or 2, the index n is 0 or 1, provided that when m is equal to 1, n is equal to 1; and when m is 2 n is 0; preferably m is equal to 1 and n is equal to one, resulting in one -[(R'O)X(RZO)S.R3] unit and R4 being present on the nitrogen. The index x is from 0 to about 50, preferably from about 3 to about 25, more preferably from about 3 to about 10.
The index y is from 0 to about 10, preferably 0, however when the index y is not equal to 0, y is from 1 to about 4. Preferably all of the alkyleneoxy units are ethyleneoxy units. Those skilled in the art of ethoxylated polyoxyalkylene alkyl amide surface active agents will recognized that the values for the indices x and y are average values and the true values may range over several values depending upon the process used to alkoxylate the amides.
The mid-chain branched alkyl sulfate surfactants of the present invention have the formula:
R R R
CH3CH2(CHZ)WCH(CH2),~CH(CH2)yCH(CHZ)ZOS03M
the alkyl alkoxy sulfates have the formula:
CH3CH2(CHZ)~,CH(CHZ)XCH(CH2)yCH(CH2)Z(OR3)",OS03M;
the alkyl alkoxylates have the formula:
CH3CH~(CHI""CH(CH~,zCH(CH~yCH(CH~(OR3~pH
wherein R, R', and RZ are each independently hydrogen, C,-C3 alkyl, and mixtures thereof;
provided at least one of R, R', and RZ is not hydrogen; preferably R, R', and RZ are methyl;
preferably one of R, R', and Rs is methyl and the other units are hydrogen.
The total number of carbon atoms in the mid-chain branched alkyl sulfate and alkyl alkoxy sulfate surfactants is from 14 to 20; the index w is an integer from 0 to 13; x is an integer from 0 to 13; y is an integer from 0 to 13; z is an integer of at least 1; provided w + x + y + z is from 8 to 14 and the total number of carbon atoms in a surfactant is from 14 to 20; R' is C,-C, linear or branched alkylene, preferably ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,4-butylene, and mixtures thereof.
However, a preferred embodiment of the present invention comprises from 1 to 3 units wherein R' is 1,2-propylene, 1,3-propylene, or mixtures thereof followed by the balance of the R' units comprising ethylene units. Another preferred embodiment comprises R' units which are randomly ethylene and 1,2-propylene units. The average value of the index m is at least about 0.01. When the index m has low values, the surfactant system comprises mostly alkyl sulfates with a small amount of alkyl alkoxy sulfate surfactant. Some tertiary carbon atoms may be present in the alkyl chain, however, this embodiment is not desired.
M denotes a cation, preferably hydrogen, a water soluble cation, and mixtures thereof.
Non-limiting examples of water soluble cations include sodium, potassium, lithium, ammonium, alkyl ammonium, and mixtures thereof.
Detergent Builder The detergent compositions herein may also comprise from about 0.1 % to 80% by weight of a detergent builder. Preferably such compositions in liquid form will comprise from about 1 % to 10% by weight of the builder component. Preferably such compositions in granular form will comprise from about 1 % to 50% by weight of the builder component.
Detergent builders are well known in the art and can comprise, for example, phosphate salts as well as various organic and inorganic nonphosphorus builders.
Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, anunonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates. Suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al., and U.S. Patent 4,246,495, issued March 27, 1979 to Crutchfield et al. Particularly preferred polycarboxylate builders are the oxydisuccinates and the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al., issued May 5, 1987.
Examples of suitable nonphosphorus, inorganic builders include the silicates, aluminosiIicates, borates and carbonates. Particularly preferred are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicates having a weight ratio of Si02 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4. Also preferred are aluminosilicates including zeolites. Such materials and their use as detergent builders are more fully discussed in Corkill et al., U.S. Patent No.
4,605,509. Also discussed in U. S. Patent No. 4,605,509 are crystalline layered silicates which are suitable for use in the detergent compositions of this invention.
Optional Detergent Ingredients In addition to the surfactants, builders and dye maintenance polymers of the detergent compositions of the present invention can also include any number of additional optional ingredients. These include conventional detergent composition components such as enzymes and enzyme stabilizing agents, suds boosters or suds suppressers, anti-tarnish and anticorrosion agents, bleaching agents, soil suspending agents, soil release agents, germicides, pH
adjusting agents, non-builder alkalinity sources, chelating. agents, organic and inorganic fillers, solvents, hydrotropes, optical brighteners, dyes and perfumes.
pH adjusting agents may be necessary in certain applications where the pH of the wash solution is greater than about 10.0 because the fabric integrity benefits of the defined compositions begin to diminish at a higher pH. Hence, if the wash solution is greater than about I0.0 after the addition of the dye maintenance polymers of the present invention a pH adjuster should be used to reduce the pH of the washing solution to below about 10.0, preferably to a pH
of below about 9.5 and most preferably below about 7.5. Suitable pH adjusters will be known to those skilled in the art.
A preferred optional ingredients for incorporation into the detergent compositions herein comprises a bleaching agent, e.g., a peroxygen bleach. Such peroxygen bleaching agents may be organic or inorganic in nature. Inorganic peroxygen bleaching agents are frequently utilized in combination with a bleach activator.
Useful organic peroxygen bleaching agents include percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of metachloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid. Such bleaching agents are disclosed in U.S. Patent 4,483,781, Hartman, Issued November 20, 1984;
European Patent Application EP-A-133,354, Banks et al., Published February 20, 1985; and U.S.
Patent 4,412,934, Chung et al., Issued November 1, 1983. Highly preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid (NAPAA) as described in U.S. Patent 4,634,551, Issued January 6, 1987 to Burns et al.
Inorganic peroxygen bleaching agents may also be used, generally in particulate form, in the detergent compositions herein. Inorganic bleaching agents are in fact preferred.
Such inorganic peroxygen compounds include alkali metal perborate and percarbonate materials.
For example, sodium perborate (e.g. mono- or tetra-hydrate) can be used.
Suitable inorganic bleaching agents can also include sodium or potassium carbonate peroxyhydrate and equivalent "percarbonate" bleaches, sodium pyrophosphate peroxyhydrate, urea peroxyhydrate, and sodium peroxide. Persulfate bleach (e.g., OXONE~, manufactured commercially by DuPont) can also be used. Frequently inorganic peroxygen bleaches will be coated with silicate, borate, sulfate or water-soluble surfactants. For example, coated percarbonate particles are available from various commercial sources such as FMC, Solway Interox, Tokai Denka and Degussa.
Inorganic peroxygen bleaching agents, e.g., the perborates, the percarbonates, etc., are preferably combined with bleach activators, which lead to the in situ production in aqueous solution (i.e., during use of the compositions herein for fabric laundering/bleaching) of the peroxy acid corresponding to the bleach activator. Various non-limiting examples of activators are disclosed in U.S, Patent 4,915,854, Issued April 10, 1990 to Mao et al.; slid U.S. Patent 4,412,934 Issued November 1, 1983 to Chung et al. The nonanoyloxybenzene sulfonate (HOBS) and tetraacetyl ethylene diamine (TAED) activators are typical and preferred.
Mixtures thereof can also be used. See also the hereinbefore referenced U.S. 4,634,551 for other typical bleaches and activators useful herein.
Other useful amido-derived bleach activators are those of the formulae:
R1N(R5)C(O)R2C(O)Lor R1C(O)N(R5)R2C(O)L
wherein R1 is an alkyl group containing from about 6 to about 12 carbon atoms, R2 is an alkylene containing from 1 to about 6 carbon atoms, R5 is H or alkyl, aryl, or alkaryl containing from about 1 to about 10 carbon atoms, and L is any suitable leaving group. A
leaving group is any group that is displaced from the bleach activator as a consequence of the nucleophilic attack on the bleach activator by the perhydrolysis anion. A preferred leaving group is phenol sulfonate.
Preferred examples of bleach activators of the above formulae include (6-octanamido-caproyl)oxybenzenesulfonate, (6-nonanamidocaproyl) oxybenzene-sulfonate, (6-decanamido-caproyl)oxybenzenesulfonate and mixtures thereof as described in the hereinbefore noted U.S. Patent 4,634,551.
Another class of useful bleach activators comprises the benzoxazin-type activators disclosed by Hodge et al. in U.S. Patent 4,966,723, Issued October 30, 1990.
See also U.S.
Patent 4,545;784, Issued to Sanderson, October 8, 1985 which discloses acyl caprolactams, including benzoyl caprolactam, adsorbed into sodium perborate.
If utilized, peroxygen bleaching agent will generally comprise from about 2%
to 30% by weight of the detergent compositions herein. More preferably, peroxygen bleaching agent will comprise from about 2% to 20% by weight of the compositions. Most preferably, peroxygen bleaching agent will be present to the extent of from about 3% to 15% by weight of the compositions herein. If utilized, bleach activators can comprise from about 2%
to 10% by weight of the detergent compositions herein. Frequently, activators are employed such that the molar ratio of bleaching agent to activator ranges from about 1:1 to 10:1, more preferably from about 1.5:1 to 5:1.
Another highly preferred optional ingredient in the detergent compositions herein is a detersive enzyme component. Enzymes can be included in the present detergent compositions for a variety of purposes, including removal of protein-based, carbohydrate-based, or triglyceride-based stains from substrates, for the prevention of refugee dye transfer in fabric laundering, and for fabric restoration. Suitable enzymes include proteases, amylases, Iipases, cellulases, peroxidases, and mixtures thereof of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. Preferred selections are influenced by factors such as pH-activity and/or stability, optimal thermostability, and stability to active detergents, builders and the like. In this respect bacterial or fungal enzymes are preferred, such as bacterial amylases and proteases, and fungal cellulases.
"Detersive enzyme", as used herein, means any enzyme having a cleaning, stain removing or otherwise beneficial effect in a laundry detergent composition.
Preferred enzymes for laundry purposes include, but are not limited to, proteases, cellulases, lipases, amylases and peroxidases.
Enzymes are normally incorporated into detergent compositions at levels sufficient to provide a "cleaning-effective amount". The term "cleaning-effective amount"
refers to any amount capable of producing a cleaning, stain removal, soil removal, whitening, deodorizing, or freshness improving effect on substrates such as fabrics. In practical terms for current commercial preparations, typical amounts are up to about 5 mg by weight, more typically 0.01 mg to 3 mg, of active enzyme per gram of the detergent composition. Stated otherwise, the compositions herein will typically comprise from 0.001% to 5%, preferably 0.01%-1% by weight of a commercial enzyme preparation. Protease enzymes are usually present in such commercial preparations at levels sufficient to provide from 0.005 to 0.1 Anson units (AU) of activity per gram of composition. Higher active levels may be desirable in highly concentrated detergent formulations.
Cellulases usable herein include those disclosed in U.S. Patent No. 4,435,307, Barbesgoard et al., March 6, 1984, and GB-A-2.075.028; GB-A-2.095.275 and DE-OS-2.247.832. CAREZYME~ and CELLUZYME~ (Novo) are especially useful. See also WO
9117243 to Novo.
The enzyme-containing compositions herein may optionally also comprise from about 0.001% to about 10%, preferably from about 0.005% to about 8%, most preferably from about 0.01% to about 6%, by weight of an enzyme stabilizing system. The enzyme stabilizing system can be any stabilizing system which is compatible with the detersive enzyme.
Such a system may be inherently provided by other formulation actives, or be added separately, e.g., by the formulator or by a manufacturer of detergent-ready enzymes. Such stabilizing systems can, for example, comprise calcium ion, boric acid, propylene glycol, short chain carboxylic acids, boronic acids, and mixtures thereof, and are designed to address different stabilization problems depending on the type and physical form of the detergent composition.
Detergent Composition Preparation The detergent compositions according to the present invention can be in liquid, paste or granular form. Such compositions can be prepared by combining the essential and optional components in the requisite concentrations in any suitable order and by any conventional means.
The forgoing description of uses for the dye maintenance polymers defined herein are intended to be exemplary and other uses will be apparent to those skilled in the art and are intended to be within the scope of the present invention.
Granular compositions, for example, are generally made by combining base granule ingredients, e.g., surfactants, builders, water, etc., as a slurry, and spray drying the resulting slurry to a low level of residual moisture (5-12%). The remaining dry ingredients, e.g., granules of the essential dye maintenance polymers, can be admixed in granular powder form with the spray dried granules in a rotary mixing drum. The liquid ingredients, e.g., solutions of the essential dye maintenance polymers, enzymes, binders and perfumes, can be sprayed onto the resulting granules to form the finished detergent composition. Granular compositions according to the present invention can also be in "compact form", i.e. they may have a relatively higher density than conventional granular detergents, i.e. from 550 to 950 g/1. In such case, the granular detergent compositions according to the present invention will contain a lower amount of "inorganic filler salt", compared to conventional granular detergents; typical filler salts are alkaline earth metal salts of sulphates and chlorides, typically sodium sulphate; "compact"
detergents typically comprise not more than 10% filler salt.
Liquid detergent compositions can be prepared by admixing the essential and optional ingredients thereof in any desired order to provide compositions containing components in the requisite concentrations. Liquid compositions according to the present invention can also be in "compact form", in such case, the liquid detergent compositions according to the present invention will contain a lower amount of water, compared to conventional liquid detergents.
Addition of the dye maintenance polymers to liquid detergent or other aqueous compositions of this invention may be accomplished by simply mixing into the liquid solutions the desired dye maintenance polymers.
Fabric Laundering_Method The present invention also provides a method for laundering fabrics in a manner which imparts fabric appearance benefits provided by the dye maintenance polymers used herein. Such a method employs contacting these fabrics with an aqueous washing solution formed from an effective amount of the detergent compositions hereinbefore described or formed from the individual components of such compositions. Contacting of fabrics with washing solution will generally occur under conditions of agitation although the compositions of the present invention may also be used to form aqueous unagitated soaking solutions for fabric cleaning and treatment.
As discussed above, it is preferred that the washing solution have a pH of less than about 10.0, preferably it has a pH of about 9.5 and most preferably it has a pH of about 7.5.
Agitation is preferably provided in a washing machine for good cleaning.
Washing is preferably followed by drying the wet fabric in a conventional clothes dryer.
An effective amount of a high density liquid or granular detergent composition in the aqueous wash solution in the washing machine is preferably from about 500 to about 7000 ppm, more preferably from about 1000 to about 3000 ppm.
EXAMPLES
The following examples illustrate the compositions and methods of the present invention, but are not necessarily meant to limit or otherwise define the scope of the invention.
EXAMPLE I
TABLE I comprises numerous examples according to the present invention albng with some comparative examples of material known to the art of laundry detergents.
The chemical structures shown in the examples below are idealized structures. Side reactions expected to occur during the condensation are not shown.
TABLEI
Ex.# Material 1 Poly(N, N dimethylaminoethyl methacrylate) 2 Poly(N, N dimethylaminoethyl methacryIate), 3 Poly(N,N dimethylaminoethyl methacrylate), MW 15,700 4 Poly(N,N dimethylaminoethyl methacrylate), MW 39,700 S Poly(N,N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratiol:l MW 13670 6 Poly(N,N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratio 2:1, MW =14,400 7 Poly(N, N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratio 3:1 MW 16,300 8 Methyl quat of poly(N,N dimethylaminoethyl methacrylate) 9 Amine oxide ofPoly(N, N dimethylaminoethyl methacrylate) Poly(N,N dimethylaminoethyl methacrylate-co-octylacrylamide) ratio 3:1, MW = 6730 11 Poly(N,N dimethylaminoethyl methacrylate-co-acrylic acid) ratio 1:1, MW = 14,950 12 Poly(N,N dimethylaminoethyl methacrylate-acrylamide) ratio 1:1, Poly(N,N dimethylaminoethyl methacrylate-propane sultone) ratio 1:1, 13 Poly(dimethyldiallylammonium chloride) sold under the trade mark Mer uat 100 b Cal on Co oration Pittsbur PA.
14 Poly(dimethyldiallylammonium chloride -co- acrylamide) sold under the trade :mark Merquat Plus (Calgon Corporation, Pittsbur , PA .
Poly(dimethyldiallylammonium chloride -co- acrylamide) sold under the trade mark Merquat 550 (Calgon Corporation, Pittsbur PA .
16 Poly(dimethyldiallylammonium chloride -co- acrylic acid) sold under the trade mark Merquat 280 (Calgon Corporation, Pittsbur PA .
17 Poly(N methyl,N octadecyl aminoethyl methacrylate) quaternized with dimeth 1 sulfate CTFA nomenclature of uaternium 8 18 Ionene polymer of N,N,N',N' tetramethyl hexanediamine and 1,6 dibromohexane in the ratio 4'3 19 Polyvinylamine 20 Poly(vinylamine-co-vinylalcohol) ratio 1:1 21 Poly(vinylamine-co-acrylic acid) ratio 1: l 22 Polyallylamine 23 poly(vinylamine-co-vinyl formamide) ratio 1:1 24 polyvinylamine ethoxylated with 0.5 moles of ethylene oxide per N-H
25 polyvinylamine propoxylated with 0.5 moles of propylene oxide er N-H
26 Polyquaternium 2 (CTFA nomenclature) sold under the trade mark Mira of A15 b Rhone Poulenc Paris, France.
27 Polyquaternium 17(CTFA nomenclature) sold under the trade mark Mira of AD-1 b Rhone Poulenc, Paris France.
28 Copolymer of N methylvinyl pyridine co-vinyl pyridine (ratio 4:1) 29 Copolymer of N methylvinyl pyridine co-vinyl pyridine (ratio 4:6) 30 Poly(N methylvinyl pyridine co-vinyl pyridine N oxide) ratio 4:1 31 Poly (N methylvinyl pyridine co-vinyl pyridine N-oxide) ratio 4:6 EXAMPLE II
Granular Detereent Test Composition Preparation Several heavy duty granular detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. These granular detergent compositions all have the following basic formula:
TABLE II
Com onent Wt.
C Linear alk 1 benzene sulfonate9.31 C a 1 ether 0.35 EO sulfate 12.74 Zeolite Builder 27.79 Sodium Carbonate 27.31 PEG 4000 1.60 Dis ersant 2.26 C Alcohol Ethoxvlate 9 EO 1.5 SodiumPerborate 1.03 Soft Release Polymer 0.41 Enz mes 0.59 D a Maintenance Polymer 3.0 Perfume, Brightener, Suds Suppressor,Balance Other Minors, Moisture, Sulfate 100%
EXAMPLE III
Liquid Detergent Test Composition Preparation Several heavy duty liquid detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. These liquid detergent compositions all have the following basic formula:
TABLE III
Com onent Wt C _ alk 1 ether 2.5 sulfate 38 C lucose amide ~ 6.86 Citric Acid 4.75 C _ Fat Acid 2.00 E mes 1.02 MEA 1.0 Pro anediol 0.36 Borax 6.58 Dis ersant 1.48 Na Toluene Sulfonate 6.25 D a Maintenance Pol mer 1.0 Dye, Perfume, Brighteners, Preservatives,Balance Suds Su ressor, Other Minors, Water 100%
EXAMPLE IV
Granular Detergent Test Composition Preparation Several granular detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. Such granular detergent compositions all have the following basic formula:
TABLE IV
Exam 1e Com arative Com onent Wt. % Wt%
Na C Linear alk 1 benzene 9.40 9.40 sulfonate Na C alk 1 sulfonate 11.26 11.26 Zeolite Builder 27.79 27.79 Sodium Carbonate 27.31 27.31 PEG 4000 1.60 1.60 Dis ersant, Na of acr 2.26 2.26 late C alk 1 ethox late 9 1.5 1.5 Sodium Perborate 1.03 1.03 D a Maintenance Pol mer 0.8 0 Other Ad'unct in redientsBalance Balance 100% 100%
CH3CH2(CHZ)WCH(CH2),~CH(CH2)yCH(CHZ)ZOS03M
the alkyl alkoxy sulfates have the formula:
CH3CH2(CHZ)~,CH(CHZ)XCH(CH2)yCH(CH2)Z(OR3)",OS03M;
the alkyl alkoxylates have the formula:
CH3CH~(CHI""CH(CH~,zCH(CH~yCH(CH~(OR3~pH
wherein R, R', and RZ are each independently hydrogen, C,-C3 alkyl, and mixtures thereof;
provided at least one of R, R', and RZ is not hydrogen; preferably R, R', and RZ are methyl;
preferably one of R, R', and Rs is methyl and the other units are hydrogen.
The total number of carbon atoms in the mid-chain branched alkyl sulfate and alkyl alkoxy sulfate surfactants is from 14 to 20; the index w is an integer from 0 to 13; x is an integer from 0 to 13; y is an integer from 0 to 13; z is an integer of at least 1; provided w + x + y + z is from 8 to 14 and the total number of carbon atoms in a surfactant is from 14 to 20; R' is C,-C, linear or branched alkylene, preferably ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,4-butylene, and mixtures thereof.
However, a preferred embodiment of the present invention comprises from 1 to 3 units wherein R' is 1,2-propylene, 1,3-propylene, or mixtures thereof followed by the balance of the R' units comprising ethylene units. Another preferred embodiment comprises R' units which are randomly ethylene and 1,2-propylene units. The average value of the index m is at least about 0.01. When the index m has low values, the surfactant system comprises mostly alkyl sulfates with a small amount of alkyl alkoxy sulfate surfactant. Some tertiary carbon atoms may be present in the alkyl chain, however, this embodiment is not desired.
M denotes a cation, preferably hydrogen, a water soluble cation, and mixtures thereof.
Non-limiting examples of water soluble cations include sodium, potassium, lithium, ammonium, alkyl ammonium, and mixtures thereof.
Detergent Builder The detergent compositions herein may also comprise from about 0.1 % to 80% by weight of a detergent builder. Preferably such compositions in liquid form will comprise from about 1 % to 10% by weight of the builder component. Preferably such compositions in granular form will comprise from about 1 % to 50% by weight of the builder component.
Detergent builders are well known in the art and can comprise, for example, phosphate salts as well as various organic and inorganic nonphosphorus builders.
Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, anunonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates. Suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al., and U.S. Patent 4,246,495, issued March 27, 1979 to Crutchfield et al. Particularly preferred polycarboxylate builders are the oxydisuccinates and the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al., issued May 5, 1987.
Examples of suitable nonphosphorus, inorganic builders include the silicates, aluminosiIicates, borates and carbonates. Particularly preferred are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicates having a weight ratio of Si02 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4. Also preferred are aluminosilicates including zeolites. Such materials and their use as detergent builders are more fully discussed in Corkill et al., U.S. Patent No.
4,605,509. Also discussed in U. S. Patent No. 4,605,509 are crystalline layered silicates which are suitable for use in the detergent compositions of this invention.
Optional Detergent Ingredients In addition to the surfactants, builders and dye maintenance polymers of the detergent compositions of the present invention can also include any number of additional optional ingredients. These include conventional detergent composition components such as enzymes and enzyme stabilizing agents, suds boosters or suds suppressers, anti-tarnish and anticorrosion agents, bleaching agents, soil suspending agents, soil release agents, germicides, pH
adjusting agents, non-builder alkalinity sources, chelating. agents, organic and inorganic fillers, solvents, hydrotropes, optical brighteners, dyes and perfumes.
pH adjusting agents may be necessary in certain applications where the pH of the wash solution is greater than about 10.0 because the fabric integrity benefits of the defined compositions begin to diminish at a higher pH. Hence, if the wash solution is greater than about I0.0 after the addition of the dye maintenance polymers of the present invention a pH adjuster should be used to reduce the pH of the washing solution to below about 10.0, preferably to a pH
of below about 9.5 and most preferably below about 7.5. Suitable pH adjusters will be known to those skilled in the art.
A preferred optional ingredients for incorporation into the detergent compositions herein comprises a bleaching agent, e.g., a peroxygen bleach. Such peroxygen bleaching agents may be organic or inorganic in nature. Inorganic peroxygen bleaching agents are frequently utilized in combination with a bleach activator.
Useful organic peroxygen bleaching agents include percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of metachloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid. Such bleaching agents are disclosed in U.S. Patent 4,483,781, Hartman, Issued November 20, 1984;
European Patent Application EP-A-133,354, Banks et al., Published February 20, 1985; and U.S.
Patent 4,412,934, Chung et al., Issued November 1, 1983. Highly preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid (NAPAA) as described in U.S. Patent 4,634,551, Issued January 6, 1987 to Burns et al.
Inorganic peroxygen bleaching agents may also be used, generally in particulate form, in the detergent compositions herein. Inorganic bleaching agents are in fact preferred.
Such inorganic peroxygen compounds include alkali metal perborate and percarbonate materials.
For example, sodium perborate (e.g. mono- or tetra-hydrate) can be used.
Suitable inorganic bleaching agents can also include sodium or potassium carbonate peroxyhydrate and equivalent "percarbonate" bleaches, sodium pyrophosphate peroxyhydrate, urea peroxyhydrate, and sodium peroxide. Persulfate bleach (e.g., OXONE~, manufactured commercially by DuPont) can also be used. Frequently inorganic peroxygen bleaches will be coated with silicate, borate, sulfate or water-soluble surfactants. For example, coated percarbonate particles are available from various commercial sources such as FMC, Solway Interox, Tokai Denka and Degussa.
Inorganic peroxygen bleaching agents, e.g., the perborates, the percarbonates, etc., are preferably combined with bleach activators, which lead to the in situ production in aqueous solution (i.e., during use of the compositions herein for fabric laundering/bleaching) of the peroxy acid corresponding to the bleach activator. Various non-limiting examples of activators are disclosed in U.S, Patent 4,915,854, Issued April 10, 1990 to Mao et al.; slid U.S. Patent 4,412,934 Issued November 1, 1983 to Chung et al. The nonanoyloxybenzene sulfonate (HOBS) and tetraacetyl ethylene diamine (TAED) activators are typical and preferred.
Mixtures thereof can also be used. See also the hereinbefore referenced U.S. 4,634,551 for other typical bleaches and activators useful herein.
Other useful amido-derived bleach activators are those of the formulae:
R1N(R5)C(O)R2C(O)Lor R1C(O)N(R5)R2C(O)L
wherein R1 is an alkyl group containing from about 6 to about 12 carbon atoms, R2 is an alkylene containing from 1 to about 6 carbon atoms, R5 is H or alkyl, aryl, or alkaryl containing from about 1 to about 10 carbon atoms, and L is any suitable leaving group. A
leaving group is any group that is displaced from the bleach activator as a consequence of the nucleophilic attack on the bleach activator by the perhydrolysis anion. A preferred leaving group is phenol sulfonate.
Preferred examples of bleach activators of the above formulae include (6-octanamido-caproyl)oxybenzenesulfonate, (6-nonanamidocaproyl) oxybenzene-sulfonate, (6-decanamido-caproyl)oxybenzenesulfonate and mixtures thereof as described in the hereinbefore noted U.S. Patent 4,634,551.
Another class of useful bleach activators comprises the benzoxazin-type activators disclosed by Hodge et al. in U.S. Patent 4,966,723, Issued October 30, 1990.
See also U.S.
Patent 4,545;784, Issued to Sanderson, October 8, 1985 which discloses acyl caprolactams, including benzoyl caprolactam, adsorbed into sodium perborate.
If utilized, peroxygen bleaching agent will generally comprise from about 2%
to 30% by weight of the detergent compositions herein. More preferably, peroxygen bleaching agent will comprise from about 2% to 20% by weight of the compositions. Most preferably, peroxygen bleaching agent will be present to the extent of from about 3% to 15% by weight of the compositions herein. If utilized, bleach activators can comprise from about 2%
to 10% by weight of the detergent compositions herein. Frequently, activators are employed such that the molar ratio of bleaching agent to activator ranges from about 1:1 to 10:1, more preferably from about 1.5:1 to 5:1.
Another highly preferred optional ingredient in the detergent compositions herein is a detersive enzyme component. Enzymes can be included in the present detergent compositions for a variety of purposes, including removal of protein-based, carbohydrate-based, or triglyceride-based stains from substrates, for the prevention of refugee dye transfer in fabric laundering, and for fabric restoration. Suitable enzymes include proteases, amylases, Iipases, cellulases, peroxidases, and mixtures thereof of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. Preferred selections are influenced by factors such as pH-activity and/or stability, optimal thermostability, and stability to active detergents, builders and the like. In this respect bacterial or fungal enzymes are preferred, such as bacterial amylases and proteases, and fungal cellulases.
"Detersive enzyme", as used herein, means any enzyme having a cleaning, stain removing or otherwise beneficial effect in a laundry detergent composition.
Preferred enzymes for laundry purposes include, but are not limited to, proteases, cellulases, lipases, amylases and peroxidases.
Enzymes are normally incorporated into detergent compositions at levels sufficient to provide a "cleaning-effective amount". The term "cleaning-effective amount"
refers to any amount capable of producing a cleaning, stain removal, soil removal, whitening, deodorizing, or freshness improving effect on substrates such as fabrics. In practical terms for current commercial preparations, typical amounts are up to about 5 mg by weight, more typically 0.01 mg to 3 mg, of active enzyme per gram of the detergent composition. Stated otherwise, the compositions herein will typically comprise from 0.001% to 5%, preferably 0.01%-1% by weight of a commercial enzyme preparation. Protease enzymes are usually present in such commercial preparations at levels sufficient to provide from 0.005 to 0.1 Anson units (AU) of activity per gram of composition. Higher active levels may be desirable in highly concentrated detergent formulations.
Cellulases usable herein include those disclosed in U.S. Patent No. 4,435,307, Barbesgoard et al., March 6, 1984, and GB-A-2.075.028; GB-A-2.095.275 and DE-OS-2.247.832. CAREZYME~ and CELLUZYME~ (Novo) are especially useful. See also WO
9117243 to Novo.
The enzyme-containing compositions herein may optionally also comprise from about 0.001% to about 10%, preferably from about 0.005% to about 8%, most preferably from about 0.01% to about 6%, by weight of an enzyme stabilizing system. The enzyme stabilizing system can be any stabilizing system which is compatible with the detersive enzyme.
Such a system may be inherently provided by other formulation actives, or be added separately, e.g., by the formulator or by a manufacturer of detergent-ready enzymes. Such stabilizing systems can, for example, comprise calcium ion, boric acid, propylene glycol, short chain carboxylic acids, boronic acids, and mixtures thereof, and are designed to address different stabilization problems depending on the type and physical form of the detergent composition.
Detergent Composition Preparation The detergent compositions according to the present invention can be in liquid, paste or granular form. Such compositions can be prepared by combining the essential and optional components in the requisite concentrations in any suitable order and by any conventional means.
The forgoing description of uses for the dye maintenance polymers defined herein are intended to be exemplary and other uses will be apparent to those skilled in the art and are intended to be within the scope of the present invention.
Granular compositions, for example, are generally made by combining base granule ingredients, e.g., surfactants, builders, water, etc., as a slurry, and spray drying the resulting slurry to a low level of residual moisture (5-12%). The remaining dry ingredients, e.g., granules of the essential dye maintenance polymers, can be admixed in granular powder form with the spray dried granules in a rotary mixing drum. The liquid ingredients, e.g., solutions of the essential dye maintenance polymers, enzymes, binders and perfumes, can be sprayed onto the resulting granules to form the finished detergent composition. Granular compositions according to the present invention can also be in "compact form", i.e. they may have a relatively higher density than conventional granular detergents, i.e. from 550 to 950 g/1. In such case, the granular detergent compositions according to the present invention will contain a lower amount of "inorganic filler salt", compared to conventional granular detergents; typical filler salts are alkaline earth metal salts of sulphates and chlorides, typically sodium sulphate; "compact"
detergents typically comprise not more than 10% filler salt.
Liquid detergent compositions can be prepared by admixing the essential and optional ingredients thereof in any desired order to provide compositions containing components in the requisite concentrations. Liquid compositions according to the present invention can also be in "compact form", in such case, the liquid detergent compositions according to the present invention will contain a lower amount of water, compared to conventional liquid detergents.
Addition of the dye maintenance polymers to liquid detergent or other aqueous compositions of this invention may be accomplished by simply mixing into the liquid solutions the desired dye maintenance polymers.
Fabric Laundering_Method The present invention also provides a method for laundering fabrics in a manner which imparts fabric appearance benefits provided by the dye maintenance polymers used herein. Such a method employs contacting these fabrics with an aqueous washing solution formed from an effective amount of the detergent compositions hereinbefore described or formed from the individual components of such compositions. Contacting of fabrics with washing solution will generally occur under conditions of agitation although the compositions of the present invention may also be used to form aqueous unagitated soaking solutions for fabric cleaning and treatment.
As discussed above, it is preferred that the washing solution have a pH of less than about 10.0, preferably it has a pH of about 9.5 and most preferably it has a pH of about 7.5.
Agitation is preferably provided in a washing machine for good cleaning.
Washing is preferably followed by drying the wet fabric in a conventional clothes dryer.
An effective amount of a high density liquid or granular detergent composition in the aqueous wash solution in the washing machine is preferably from about 500 to about 7000 ppm, more preferably from about 1000 to about 3000 ppm.
EXAMPLES
The following examples illustrate the compositions and methods of the present invention, but are not necessarily meant to limit or otherwise define the scope of the invention.
EXAMPLE I
TABLE I comprises numerous examples according to the present invention albng with some comparative examples of material known to the art of laundry detergents.
The chemical structures shown in the examples below are idealized structures. Side reactions expected to occur during the condensation are not shown.
TABLEI
Ex.# Material 1 Poly(N, N dimethylaminoethyl methacrylate) 2 Poly(N, N dimethylaminoethyl methacryIate), 3 Poly(N,N dimethylaminoethyl methacrylate), MW 15,700 4 Poly(N,N dimethylaminoethyl methacrylate), MW 39,700 S Poly(N,N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratiol:l MW 13670 6 Poly(N,N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratio 2:1, MW =14,400 7 Poly(N, N dimethylaminoethyl methacrylate-co-dimethylacrylamide) ratio 3:1 MW 16,300 8 Methyl quat of poly(N,N dimethylaminoethyl methacrylate) 9 Amine oxide ofPoly(N, N dimethylaminoethyl methacrylate) Poly(N,N dimethylaminoethyl methacrylate-co-octylacrylamide) ratio 3:1, MW = 6730 11 Poly(N,N dimethylaminoethyl methacrylate-co-acrylic acid) ratio 1:1, MW = 14,950 12 Poly(N,N dimethylaminoethyl methacrylate-acrylamide) ratio 1:1, Poly(N,N dimethylaminoethyl methacrylate-propane sultone) ratio 1:1, 13 Poly(dimethyldiallylammonium chloride) sold under the trade mark Mer uat 100 b Cal on Co oration Pittsbur PA.
14 Poly(dimethyldiallylammonium chloride -co- acrylamide) sold under the trade :mark Merquat Plus (Calgon Corporation, Pittsbur , PA .
Poly(dimethyldiallylammonium chloride -co- acrylamide) sold under the trade mark Merquat 550 (Calgon Corporation, Pittsbur PA .
16 Poly(dimethyldiallylammonium chloride -co- acrylic acid) sold under the trade mark Merquat 280 (Calgon Corporation, Pittsbur PA .
17 Poly(N methyl,N octadecyl aminoethyl methacrylate) quaternized with dimeth 1 sulfate CTFA nomenclature of uaternium 8 18 Ionene polymer of N,N,N',N' tetramethyl hexanediamine and 1,6 dibromohexane in the ratio 4'3 19 Polyvinylamine 20 Poly(vinylamine-co-vinylalcohol) ratio 1:1 21 Poly(vinylamine-co-acrylic acid) ratio 1: l 22 Polyallylamine 23 poly(vinylamine-co-vinyl formamide) ratio 1:1 24 polyvinylamine ethoxylated with 0.5 moles of ethylene oxide per N-H
25 polyvinylamine propoxylated with 0.5 moles of propylene oxide er N-H
26 Polyquaternium 2 (CTFA nomenclature) sold under the trade mark Mira of A15 b Rhone Poulenc Paris, France.
27 Polyquaternium 17(CTFA nomenclature) sold under the trade mark Mira of AD-1 b Rhone Poulenc, Paris France.
28 Copolymer of N methylvinyl pyridine co-vinyl pyridine (ratio 4:1) 29 Copolymer of N methylvinyl pyridine co-vinyl pyridine (ratio 4:6) 30 Poly(N methylvinyl pyridine co-vinyl pyridine N oxide) ratio 4:1 31 Poly (N methylvinyl pyridine co-vinyl pyridine N-oxide) ratio 4:6 EXAMPLE II
Granular Detereent Test Composition Preparation Several heavy duty granular detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. These granular detergent compositions all have the following basic formula:
TABLE II
Com onent Wt.
C Linear alk 1 benzene sulfonate9.31 C a 1 ether 0.35 EO sulfate 12.74 Zeolite Builder 27.79 Sodium Carbonate 27.31 PEG 4000 1.60 Dis ersant 2.26 C Alcohol Ethoxvlate 9 EO 1.5 SodiumPerborate 1.03 Soft Release Polymer 0.41 Enz mes 0.59 D a Maintenance Polymer 3.0 Perfume, Brightener, Suds Suppressor,Balance Other Minors, Moisture, Sulfate 100%
EXAMPLE III
Liquid Detergent Test Composition Preparation Several heavy duty liquid detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. These liquid detergent compositions all have the following basic formula:
TABLE III
Com onent Wt C _ alk 1 ether 2.5 sulfate 38 C lucose amide ~ 6.86 Citric Acid 4.75 C _ Fat Acid 2.00 E mes 1.02 MEA 1.0 Pro anediol 0.36 Borax 6.58 Dis ersant 1.48 Na Toluene Sulfonate 6.25 D a Maintenance Pol mer 1.0 Dye, Perfume, Brighteners, Preservatives,Balance Suds Su ressor, Other Minors, Water 100%
EXAMPLE IV
Granular Detergent Test Composition Preparation Several granular detergent compositions are prepared containing one or more dye maintenance polymer having a DMP according to this invention. Such granular detergent compositions all have the following basic formula:
TABLE IV
Exam 1e Com arative Com onent Wt. % Wt%
Na C Linear alk 1 benzene 9.40 9.40 sulfonate Na C alk 1 sulfonate 11.26 11.26 Zeolite Builder 27.79 27.79 Sodium Carbonate 27.31 27.31 PEG 4000 1.60 1.60 Dis ersant, Na of acr 2.26 2.26 late C alk 1 ethox late 9 1.5 1.5 Sodium Perborate 1.03 1.03 D a Maintenance Pol mer 0.8 0 Other Ad'unct in redientsBalance Balance 100% 100%
Claims (10)
1. A detergent composition comprising:
a) from 4% to 70% by weight, of a surfactant;
b) from 0.01% to 10% by weight, of a dye maintenance co-polymer, said copolymer having the general formula:
x has the value of from 10 to 100,000; y has the value of from 10 to 100,000;
the ratio of x to y is from 9:1 to 1:9; each Z is independently (CH2)m COR' wherein R' is selected from:
i) -OR3;
ii) -O(CH2)n N(R3)2;
iii) -O(CH2)n N+(R3)3X-;
iv) -NR3(CH2)n N(R3)2;
v) -NR3(CH2)n N+(R3)3X-;
vi) -(CH2)n N(R3)2;
vii) -(CH2)n N+(R3)3X-;
viii) and mixtures thereof;
each R3 is independently hydrogen, C1-C8 alkyl, C2-C8 hydroxyalkyl, or mixtures thereof; X is a water soluble anion; the index n is from 0 to 6; the index m is from 0 to 6;
provided said co-polymer has a net cationic charge; and wherein said dye maintenance co-polymer is not an polyethyleneimine or alkoxylated derivative thereof; and c) the balance carriers and other adjunct ingredients.
a) from 4% to 70% by weight, of a surfactant;
b) from 0.01% to 10% by weight, of a dye maintenance co-polymer, said copolymer having the general formula:
x has the value of from 10 to 100,000; y has the value of from 10 to 100,000;
the ratio of x to y is from 9:1 to 1:9; each Z is independently (CH2)m COR' wherein R' is selected from:
i) -OR3;
ii) -O(CH2)n N(R3)2;
iii) -O(CH2)n N+(R3)3X-;
iv) -NR3(CH2)n N(R3)2;
v) -NR3(CH2)n N+(R3)3X-;
vi) -(CH2)n N(R3)2;
vii) -(CH2)n N+(R3)3X-;
viii) and mixtures thereof;
each R3 is independently hydrogen, C1-C8 alkyl, C2-C8 hydroxyalkyl, or mixtures thereof; X is a water soluble anion; the index n is from 0 to 6; the index m is from 0 to 6;
provided said co-polymer has a net cationic charge; and wherein said dye maintenance co-polymer is not an polyethyleneimine or alkoxylated derivative thereof; and c) the balance carriers and other adjunct ingredients.
2. A composition according to Claim 1 comprising from 0.1% to 7% by weight of said dye maintenance co-polymer.
3. A composition according to Claim 1 wherein Z has the formula:
4. A composition according to Claim 1 wherein dye maintenance co-polymer further comprises a cyclically polymerizing monomer, said cyclically polymerizing monomer having the formula:
wherein R5 is C1-C4 alkyl, and mixtures thereof; X is a water soluble anion.
wherein R5 is C1-C4 alkyl, and mixtures thereof; X is a water soluble anion.
5. A composition according to Claim 1 comprising a co-polymer wherein Z has the formula:
-(CH2)m COR' wherein each R' is independently -O(CH2)n N(R3)2; -O(CH2)n N+(R3)3X-; -(CH2)n N(R3)2;
-(CH2)n N+(R3)3X-; or mixtures thereof, m is 0, n is from 2 to 4.
-(CH2)m COR' wherein each R' is independently -O(CH2)n N(R3)2; -O(CH2)n N+(R3)3X-; -(CH2)n N(R3)2;
-(CH2)n N+(R3)3X-; or mixtures thereof, m is 0, n is from 2 to 4.
6. A composition according to Claim 1 comprising a co-polymer wherein the co-polymer further comprises vinyl amine units having the formula:
wherein x' + x'' = x.
wherein x' + x'' = x.
7. A composition according to Claim 6 wherein Z comprises a polymerizing monomer, said polymerizing monomer having the formula:
wherein R1 and R2 are each hydrogen and R6 is methyl.
wherein R1 and R2 are each hydrogen and R6 is methyl.
8. A composition according to Claim 6 wherein Z comprises a polymerizing monomer, said polymerizing monomer having the formula:
wherein R1 and R2 are each hydrogen.
wherein R1 and R2 are each hydrogen.
9. A composition according to Claim 1 wherein said adjunct ingredients are selected from the group consisting of electrolytes, stabilizers, low molecular weight water soluble solvents, chelating agents, dispersibility aids, soil release agents, nonionic fabric softening agents, concentration aid, perfume, preservatives, colorants, optical brighteners, opacifiers, germicides, fungicides, anti-corrosion agents, antifoam agents, and mixtures thereof.
10. A method for reducing the loss of fabric dye comprising the steps of:
i) contacting dyed fabric with a laundry detergent comprising:
a) from 4% to 70% by weight, of a surfactant;
b) from 0.01 % to 5% by weight, of the dye maintenance copolymer of Claim 1; and c) the balance carriers and other adjunct ingredients;
ii) agitation; and iii) optionally, drying the fabric.
i) contacting dyed fabric with a laundry detergent comprising:
a) from 4% to 70% by weight, of a surfactant;
b) from 0.01 % to 5% by weight, of the dye maintenance copolymer of Claim 1; and c) the balance carriers and other adjunct ingredients;
ii) agitation; and iii) optionally, drying the fabric.
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US12607299P | 1999-03-25 | 1999-03-25 | |
US60/126,072 | 1999-03-25 | ||
PCT/US2000/008031 WO2000056849A1 (en) | 1999-03-25 | 2000-03-24 | Laundry detergent compositions with certain cationically charged dye maintenance polymers |
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CA002365303A Expired - Fee Related CA2365303C (en) | 1999-03-25 | 2000-03-24 | Laundry detergent compositions with certain cationically charged dye maintenance polymers |
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JP (2) | JP4601829B2 (en) |
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US6733538B1 (en) * | 1999-03-25 | 2004-05-11 | The Procter & Gamble Company | Laundry detergent compositions with certain cationically charged dye maintenance polymers |
DE10027634A1 (en) * | 2000-06-06 | 2001-12-13 | Basf Ag | Use of hydrophobic polymer particles, cationically modified by coating with cationic polymer, as additives in washing or care materials for textiles and as additives in detergents |
EP1239025A3 (en) * | 2001-03-03 | 2003-09-03 | Clariant GmbH | Detergent composition and laundry treatment compositon comprising dye transfer inhibiting and dye fixing agent |
DE10150724A1 (en) * | 2001-03-03 | 2003-04-17 | Clariant Gmbh | Washing agents such as detergents contain dye transfer inhibitors which are polyamine/cyanamide/amidosulfuric acid, cyanamide/aldehyde/ammonium salt or amine/epichlorhydrin reaction products |
US7799421B2 (en) | 2002-02-14 | 2010-09-21 | Akzo Nobel N.V. | Controlled release materials |
US6924259B2 (en) | 2002-04-17 | 2005-08-02 | National Starch And Chemical Investment Holding Corporation | Amine copolymers for textile and fabric protection |
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-
2000
- 2000-03-24 BR BR0009279-7A patent/BR0009279A/en not_active Application Discontinuation
- 2000-03-24 DE DE60020091T patent/DE60020091T2/en not_active Expired - Lifetime
- 2000-03-24 EP EP00918421A patent/EP1163319B1/en not_active Expired - Lifetime
- 2000-03-24 MX MXPA01009728A patent/MXPA01009728A/en active IP Right Grant
- 2000-03-24 AU AU39235/00A patent/AU3923500A/en not_active Abandoned
- 2000-03-24 JP JP2000606707A patent/JP4601829B2/en not_active Expired - Fee Related
- 2000-03-24 EP EP00918422A patent/EP1163320A1/en not_active Ceased
- 2000-03-24 AT AT00918421T patent/ATE295405T1/en not_active IP Right Cessation
- 2000-03-24 AU AU39234/00A patent/AU3923400A/en not_active Abandoned
- 2000-03-24 CN CN00807785.1A patent/CN1280391C/en not_active Expired - Fee Related
- 2000-03-24 ES ES00918421T patent/ES2242612T3/en not_active Expired - Lifetime
- 2000-03-24 CA CA002365282A patent/CA2365282C/en not_active Expired - Lifetime
- 2000-03-24 WO PCT/US2000/008031 patent/WO2000056849A1/en not_active Application Discontinuation
- 2000-03-24 AR ARP000101326A patent/AR023156A1/en active IP Right Grant
- 2000-03-24 CA CA002365303A patent/CA2365303C/en not_active Expired - Fee Related
- 2000-03-24 WO PCT/US2000/008030 patent/WO2000056848A1/en active IP Right Grant
- 2000-03-24 JP JP2000606708A patent/JP2002540250A/en not_active Withdrawn
- 2000-03-24 AR ARP000101325A patent/AR023155A1/en unknown
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WO2000056849A1 (en) | 2000-09-28 |
AR023155A1 (en) | 2002-09-04 |
WO2000056848A1 (en) | 2000-09-28 |
EP1163319A1 (en) | 2001-12-19 |
MXPA01009728A (en) | 2002-03-14 |
BR0009279A (en) | 2001-12-26 |
DE60020091D1 (en) | 2005-06-16 |
AU3923400A (en) | 2000-10-09 |
ES2242612T3 (en) | 2005-11-16 |
CA2365303A1 (en) | 2000-09-28 |
CN1351644A (en) | 2002-05-29 |
CN1280391C (en) | 2006-10-18 |
JP2002540301A (en) | 2002-11-26 |
EP1163319B1 (en) | 2005-05-11 |
JP4601829B2 (en) | 2010-12-22 |
CA2365282C (en) | 2007-01-30 |
AR023156A1 (en) | 2002-09-04 |
AU3923500A (en) | 2000-10-09 |
DE60020091T2 (en) | 2006-03-09 |
ATE295405T1 (en) | 2005-05-15 |
JP2002540250A (en) | 2002-11-26 |
EP1163320A1 (en) | 2001-12-19 |
CA2365282A1 (en) | 2000-09-28 |
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