CA3199892A1 - Colour care detergent composition - Google Patents
Colour care detergent compositionInfo
- Publication number
- CA3199892A1 CA3199892A1 CA3199892A CA3199892A CA3199892A1 CA 3199892 A1 CA3199892 A1 CA 3199892A1 CA 3199892 A CA3199892 A CA 3199892A CA 3199892 A CA3199892 A CA 3199892A CA 3199892 A1 CA3199892 A1 CA 3199892A1
- Authority
- CA
- Canada
- Prior art keywords
- surfactant
- detergent composition
- alkyl
- copolymer
- laundry detergent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 168
- 239000003599 detergent Substances 0.000 title claims abstract description 83
- 239000004744 fabric Substances 0.000 claims abstract description 74
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 42
- 229920006317 cationic polymer Polymers 0.000 claims abstract description 35
- 239000004094 surface-active agent Substances 0.000 claims description 83
- -1 acryl Chemical group 0.000 claims description 71
- 239000000975 dye Substances 0.000 claims description 49
- 229920001577 copolymer Polymers 0.000 claims description 45
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 40
- 125000000217 alkyl group Chemical group 0.000 claims description 37
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 27
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 26
- 239000003945 anionic surfactant Substances 0.000 claims description 25
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 claims description 22
- 238000007046 ethoxylation reaction Methods 0.000 claims description 19
- 238000004900 laundering Methods 0.000 claims description 17
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 16
- 150000001412 amines Chemical class 0.000 claims description 12
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 10
- 239000000985 reactive dye Substances 0.000 claims description 9
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims description 8
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
- 239000002280 amphoteric surfactant Substances 0.000 claims description 7
- 239000000986 disperse dye Substances 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 claims description 5
- 239000002888 zwitterionic surfactant Substances 0.000 claims description 5
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 4
- 230000014759 maintenance of location Effects 0.000 claims description 4
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical group CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical compound Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 229940048053 acrylate Drugs 0.000 claims 1
- 230000000740 bleeding effect Effects 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 description 34
- 238000004140 cleaning Methods 0.000 description 24
- 239000007788 liquid Substances 0.000 description 21
- 238000000034 method Methods 0.000 description 19
- 239000000243 solution Substances 0.000 description 18
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 17
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 16
- 102000004190 Enzymes Human genes 0.000 description 14
- 108090000790 Enzymes Proteins 0.000 description 14
- 229940088598 enzyme Drugs 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229920000742 Cotton Polymers 0.000 description 11
- 241000219146 Gossypium Species 0.000 description 11
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 11
- 238000012546 transfer Methods 0.000 description 11
- 229920000289 Polyquaternium Polymers 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 229920000728 polyester Polymers 0.000 description 10
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 9
- 239000002775 capsule Substances 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 8
- 150000004996 alkyl benzenes Chemical class 0.000 description 8
- 238000003795 desorption Methods 0.000 description 8
- 239000002689 soil Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 7
- 230000002401 inhibitory effect Effects 0.000 description 7
- 239000002304 perfume Substances 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 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 6
- 239000002253 acid Substances 0.000 description 6
- 238000005562 fading Methods 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000013504 Triton X-100 Substances 0.000 description 5
- 229920004890 Triton X-100 Polymers 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000004519 grease Substances 0.000 description 5
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 239000003752 hydrotrope Substances 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 238000000862 absorption spectrum Methods 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 235000010216 calcium carbonate Nutrition 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 108090000854 Oxidoreductases Proteins 0.000 description 3
- 102000004316 Oxidoreductases Human genes 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000982 direct dye Substances 0.000 description 3
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000007850 fluorescent dye Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000004676 glycans Chemical class 0.000 description 3
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical class NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical group C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 3
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 description 2
- UGIJCMNGQCUTPI-UHFFFAOYSA-N 2-aminoethyl prop-2-enoate Chemical compound NCCOC(=O)C=C UGIJCMNGQCUTPI-UHFFFAOYSA-N 0.000 description 2
- 108010065511 Amylases Proteins 0.000 description 2
- 102000013142 Amylases Human genes 0.000 description 2
- QZTXZQIFZTVMHI-UHFFFAOYSA-N C(CC)C(COCCOCCOCCO)CCCCC Chemical compound C(CC)C(COCCOCCOCCO)CCCCC QZTXZQIFZTVMHI-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 229940120146 EDTMP Drugs 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 108090001060 Lipase Proteins 0.000 description 2
- 102000004882 Lipase Human genes 0.000 description 2
- 239000004367 Lipase Substances 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical class CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 2
- DUJHUESDNVWCBZ-UHFFFAOYSA-N [acetyloxy(2-hydroxyethyl)amino] acetate Chemical compound CC(=O)ON(CCO)OC(C)=O DUJHUESDNVWCBZ-UHFFFAOYSA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- PDIZYYQQWUOPPK-UHFFFAOYSA-N acetic acid;2-(methylamino)acetic acid Chemical compound CC(O)=O.CC(O)=O.CNCC(O)=O PDIZYYQQWUOPPK-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000005233 alkylalcohol group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 235000019418 amylase Nutrition 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000008406 cosmetic ingredient Substances 0.000 description 2
- 108010005400 cutinase Proteins 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 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 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 2
- 229960001484 edetic acid Drugs 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229940080260 iminodisuccinate Drugs 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 235000019421 lipase Nutrition 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- VMESOKCXSYNAKD-UHFFFAOYSA-N n,n-dimethylhydroxylamine Chemical compound CN(C)O VMESOKCXSYNAKD-UHFFFAOYSA-N 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 108090000765 processed proteins & peptides Chemical class 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- 239000000984 vat dye Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000008096 xylene Chemical class 0.000 description 2
- HYYXZCHMGNWJQL-BYPYZUCNSA-N (2s)-2-[bis(carboxymethyl)amino]-3-hydroxypropanoic acid Chemical class OC[C@@H](C(O)=O)N(CC(O)=O)CC(O)=O HYYXZCHMGNWJQL-BYPYZUCNSA-N 0.000 description 1
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- 229920003067 (meth)acrylic acid ester copolymer Polymers 0.000 description 1
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 1
- MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- WZZLKARCGWTTIC-UHFFFAOYSA-N 13-methylpentadecyl hydrogen sulfate Chemical class CCC(C)CCCCCCCCCCCCOS(O)(=O)=O WZZLKARCGWTTIC-UHFFFAOYSA-N 0.000 description 1
- VZYDKJOUEPFKMW-UHFFFAOYSA-N 2,3-dihydroxybenzenesulfonic acid Chemical class OC1=CC=CC(S(O)(=O)=O)=C1O VZYDKJOUEPFKMW-UHFFFAOYSA-N 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
- 230000003716 rejuvenation Effects 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 108010038851 tannase Proteins 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 150000003732 xanthenes Chemical class 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
-
- 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
- C11D3/37—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
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)
Abstract
The need for a detergent composition which provides reduced dye bleeding from fabrics, is met by formulating the composition using a combination of branched nonionic surfactant and cationic polymer.
Description
COLOUR CARE DETERGENT COMPOSITION
FIELD OF THE INVENTION
Laundry detergent compositions, especially liquid laundry detergent compositions or unit dose articles providing improved care of coloured fabric.
BACKGROUND OF THE INVENTION
Laundry detergent compositions are formulated to provide good cleaning to fabrics: To keep white fabrics white, and to keep coloured fabrics bright. The laundry detergent compositions are also typically formulated to remove stains and soils. However, in addition to removing soils, the laundry detergent compositions have been known to also remove dyes from coloured fabrics, resulting in fading of coloured fabrics In addition, the dyes can deposit onto other fabrics being washed in the same cycle, resulting in discoloration of the co-washed fabrics.
In order to limit dye transfer to co-washed fabrics, dye-transfer inhibiting (DTI) polymers are often incorporated into detergent compositions marketed for cleaning coloured fabrics. Typical dye-transfer inhibitors are typically based on polymers such as polyvinyl pyrrolidone homopolymers (PVP), polyvinyl pyrrolidone / polyvinyl imidazole copolymers (PVP/PVI), and poly-4-vinylpyridine N-oxide (PVNO). However, while such DTI polymers reduce dye-transfer to co-washed fabric, they do not prevent dye bleeding from fabrics which leads to dye-fading.
As such, a need remains for a detergent composition which provides reduced dye bleeding from fabrics.
W02010025116A1 relates to stable colour maintenance and/or rejuvenation compositions comprising at least one cationic polymer and anionic surfactant, and methods for providing the same. W02013070560A1 relates to surface treatment compositions comprising certain cationic polymer(s), anionic surfactant, one or more shielding salts and hydrophobic association disruptor, the surface treatment compositions comprises at least 6 % by weight of cationic polymer, at least 6% by weight anionic surfactant, and at least 4 % by weight of the shielding salt, the weight ratio of anionic surfactant to cationic polymer is between 0.5:1 and 4:1, the composition may also have a weight ratio of shielding salt to cationic polymer of between 0.3:1 and 3:1.
relates to a method of reducing dye loss during the laundry treatment of dyed fabrics using a laundry treatment composition comprising a water-soluble or water-dispersible rebuild agent for
FIELD OF THE INVENTION
Laundry detergent compositions, especially liquid laundry detergent compositions or unit dose articles providing improved care of coloured fabric.
BACKGROUND OF THE INVENTION
Laundry detergent compositions are formulated to provide good cleaning to fabrics: To keep white fabrics white, and to keep coloured fabrics bright. The laundry detergent compositions are also typically formulated to remove stains and soils. However, in addition to removing soils, the laundry detergent compositions have been known to also remove dyes from coloured fabrics, resulting in fading of coloured fabrics In addition, the dyes can deposit onto other fabrics being washed in the same cycle, resulting in discoloration of the co-washed fabrics.
In order to limit dye transfer to co-washed fabrics, dye-transfer inhibiting (DTI) polymers are often incorporated into detergent compositions marketed for cleaning coloured fabrics. Typical dye-transfer inhibitors are typically based on polymers such as polyvinyl pyrrolidone homopolymers (PVP), polyvinyl pyrrolidone / polyvinyl imidazole copolymers (PVP/PVI), and poly-4-vinylpyridine N-oxide (PVNO). However, while such DTI polymers reduce dye-transfer to co-washed fabric, they do not prevent dye bleeding from fabrics which leads to dye-fading.
As such, a need remains for a detergent composition which provides reduced dye bleeding from fabrics.
W02010025116A1 relates to stable colour maintenance and/or rejuvenation compositions comprising at least one cationic polymer and anionic surfactant, and methods for providing the same. W02013070560A1 relates to surface treatment compositions comprising certain cationic polymer(s), anionic surfactant, one or more shielding salts and hydrophobic association disruptor, the surface treatment compositions comprises at least 6 % by weight of cationic polymer, at least 6% by weight anionic surfactant, and at least 4 % by weight of the shielding salt, the weight ratio of anionic surfactant to cationic polymer is between 0.5:1 and 4:1, the composition may also have a weight ratio of shielding salt to cationic polymer of between 0.3:1 and 3:1.
relates to a method of reducing dye loss during the laundry treatment of dyed fabrics using a laundry treatment composition comprising a water-soluble or water-dispersible rebuild agent for
2 deposition onto a fabric during a treatment process wherein the material undergoes during the treatment process, a chemical change by which change the affinity of the material for the fabric is increased. W02014139577A1 relates to a two-component colour detergent composition for use at low temperature comprising or consisting of a first component comprising at least one non-ionic surfactant, and a second component comprising at least one percarbonate (a bleach), and tetraacetylethylenediamine (TAED), as well as to a method for preparing such two-component colour detergent composition and to their use for cleaning laundry items, in particular coloured laundry items. W02017/044749A1 relates to a laundry or cleaning composition comprising (i) from about 0.001 wt. % to about 50 wt. % of at least one cationic polymer selected from the group consisting of poly acrylamidopropyl trimethyl ammonium chloride Poly (APT AC), polydiallyl dimethyl ammonium chloride poly(DADMAC), copolymers of polyAPTAC, copolymers of polyDADMAC, terpolymers of polyAPTAC, and/or terpolymers of polyDADMAC; (ii) from about 0.01 wt.% to about 50 wt.% of at least one non-ionic surfactant; (iii) optionally, from about 0.001 wt.% to about 5 wt.% of at least one enzyme; and (iv) optionally, from about 0.01 wt.% to about 25 wt.% of at least one laundry or cleaning additive, wherein said composition is capable of exhibiting color wash fastness or color maintenance.
SUMMARY OF THE INVENTION
The present invention relates to a laundry detergent composition comprising a surfactant system and cationic polymer, wherein the surfactant system comprises: a branched nonionic surfactant, and wherein the cationic polymer is selected from: poly (diallyldimethylammonium chloride); copolymer of diallyldimethylammonium chloride and acrylic acid;
copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride; copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid; copolymer of acrylamide and N,N, N-trimethyl aminoethyl acrylate; copolymer of diallyldimethylammonium chloride and vinyl alcohol, and mixtures thereof, wherein the cationic polymer has a molecular weight of from 1,000 Da to 1,250,000 Da, wherein the branched nonionic surfactant selected from:
Formula I: R1-CH(R2)-0-(P0)x(E0)y(P0)z-H, wherein, in Formula I: R1 is a C4 to C14 alkyl chain, preferably C4 to CS, more preferably C6, R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably
SUMMARY OF THE INVENTION
The present invention relates to a laundry detergent composition comprising a surfactant system and cationic polymer, wherein the surfactant system comprises: a branched nonionic surfactant, and wherein the cationic polymer is selected from: poly (diallyldimethylammonium chloride); copolymer of diallyldimethylammonium chloride and acrylic acid;
copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride; copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid; copolymer of acrylamide and N,N, N-trimethyl aminoethyl acrylate; copolymer of diallyldimethylammonium chloride and vinyl alcohol, and mixtures thereof, wherein the cationic polymer has a molecular weight of from 1,000 Da to 1,250,000 Da, wherein the branched nonionic surfactant selected from:
Formula I: R1-CH(R2)-0-(P0)x(E0)y(P0)z-H, wherein, in Formula I: R1 is a C4 to C14 alkyl chain, preferably C4 to CS, more preferably C6, R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably
3 C3 alkyl chain, x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3, y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12, z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, EO stands for ethoxylation and PO stands for propoxylation;
Formula II: R1-CH(R2)CH2-0-(P0)õ(E0)y(P0)z-H, wherein in formula II: R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5, R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain, xis from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3, y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12, z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, EO stands for ethoxylation and PO
stands for propoxylation; and mixtures thereof.
The present invention further relates to the use of a laundry detergent composition comprising a branched nonionic surfactant for improving the colour protection, preferably colour retention, of coloured fabrics during laundering.
DETAILED DESCRIPTION OF THE INVENTION
The detergent compositions of the present invention have been found to result in reduced dye fading during laundering.
Unless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.
All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated.
All measurements are performed at 25 C unless otherwise specified.
As used herein, the articles including "a" and "an" when used in a claim, are understood to mean one or more of what is claimed or described.
Laundry detergent composition:
The laundry detergent composition can be in any suitable form, such as liquid, paste, granular, solid, powder, or in conjunction with a carrier such as a substrate.
Preferred laundry detergent compositions are either liquid or granular, with liquid being most preferred.
As used herein, "liquid detergent composition" refers to liquid detergent composition which is fluid, and preferably capable of wetting and cleaning a fabric, e.g., clothing in a domestic washing
Formula II: R1-CH(R2)CH2-0-(P0)õ(E0)y(P0)z-H, wherein in formula II: R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5, R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain, xis from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3, y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12, z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, EO stands for ethoxylation and PO
stands for propoxylation; and mixtures thereof.
The present invention further relates to the use of a laundry detergent composition comprising a branched nonionic surfactant for improving the colour protection, preferably colour retention, of coloured fabrics during laundering.
DETAILED DESCRIPTION OF THE INVENTION
The detergent compositions of the present invention have been found to result in reduced dye fading during laundering.
Unless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.
All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated.
All measurements are performed at 25 C unless otherwise specified.
As used herein, the articles including "a" and "an" when used in a claim, are understood to mean one or more of what is claimed or described.
Laundry detergent composition:
The laundry detergent composition can be in any suitable form, such as liquid, paste, granular, solid, powder, or in conjunction with a carrier such as a substrate.
Preferred laundry detergent compositions are either liquid or granular, with liquid being most preferred.
As used herein, "liquid detergent composition" refers to liquid detergent composition which is fluid, and preferably capable of wetting and cleaning a fabric, e.g., clothing in a domestic washing
4 machine. As used herein, "laundry detergent composition" refers to compositions suitable for washing clothes. The composition can include solids or gases in suitably subdivided form, but the overall composition excludes product forms which are non-fluid overall, such as tablets or granules. The liquid laundry detergent composition preferably has a density in the range from 0.9 to 1.3 grams per cubic centimetre, more specifically from 1.00 to 1.10 grams per cubic centimetre, excluding any solid additives but including any bubbles, if present.
The composition can be an aqueous liquid laundry detergent composition. For such aqueous liquid laundry detergent compositions, the water content can be present at a level of from 50 % to 95 %, preferably from 25 % to 90 %, more preferably from 50 % to 85 % by weight of the liquid detergent composition.
The pH range of the detergent composition is from 6.0 to 8.9, preferably from pH 7 to 8.8.
The detergent composition can also be encapsulated in a water-soluble film, to form a unit dose article. Such unit dose articles comprise a detergent composition of the present invention, wherein the detergent composition comprises less than 20%, preferably less than 15%, more preferably less than 10% by weight of water, and the detergent composition is enclosed in a water-soluble or dispersible film. Such unit-dose articles can be formed using any means known in the art. Suitable unit-dose articles can comprise one compartment, wherein the compartment comprises the liquid laundry detergent composition. Alternatively, the unit-dose articles can be multi-compartment unit-dose articles, wherein at least one compartment comprises the liquid laundry detergent composition.
Cationic polymer The cationic polymer is selected from the group consisting of: poly (diallyldimethylammonium chloride) (polyquaternium 6);
copolymer of diallyldimethylammonium chloride and acrylic acid (such as polyquaternium 22);
copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride (polyquaternium 7); copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (polyquaternium 47);
copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (polyquaternium 53); copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid (polyquaternium 39); copolymer of acrylamide and N,N, N-trimethyl aminoethyl acrylate;
copolymer of diallyldimethylammonium chloride and vinyl alcohol; and mixtures thereof, preferably from the group consisting of: the cationic polymer is selected from: poly (diallyldimethylammonium chloride) (such as polyquatemium 6); copolymer of diallyldimethylammonium chloride and acrylic acid (such as polyquatemium 22);
copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (such as
The composition can be an aqueous liquid laundry detergent composition. For such aqueous liquid laundry detergent compositions, the water content can be present at a level of from 50 % to 95 %, preferably from 25 % to 90 %, more preferably from 50 % to 85 % by weight of the liquid detergent composition.
The pH range of the detergent composition is from 6.0 to 8.9, preferably from pH 7 to 8.8.
The detergent composition can also be encapsulated in a water-soluble film, to form a unit dose article. Such unit dose articles comprise a detergent composition of the present invention, wherein the detergent composition comprises less than 20%, preferably less than 15%, more preferably less than 10% by weight of water, and the detergent composition is enclosed in a water-soluble or dispersible film. Such unit-dose articles can be formed using any means known in the art. Suitable unit-dose articles can comprise one compartment, wherein the compartment comprises the liquid laundry detergent composition. Alternatively, the unit-dose articles can be multi-compartment unit-dose articles, wherein at least one compartment comprises the liquid laundry detergent composition.
Cationic polymer The cationic polymer is selected from the group consisting of: poly (diallyldimethylammonium chloride) (polyquaternium 6);
copolymer of diallyldimethylammonium chloride and acrylic acid (such as polyquaternium 22);
copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride (polyquaternium 7); copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (polyquaternium 47);
copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (polyquaternium 53); copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid (polyquaternium 39); copolymer of acrylamide and N,N, N-trimethyl aminoethyl acrylate;
copolymer of diallyldimethylammonium chloride and vinyl alcohol; and mixtures thereof, preferably from the group consisting of: the cationic polymer is selected from: poly (diallyldimethylammonium chloride) (such as polyquatemium 6); copolymer of diallyldimethylammonium chloride and acrylic acid (such as polyquatemium 22);
copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid (such as
5 polyquaternium 47); and mixtures thereof, more preferably the cationic polymer is copolymer of diallyldimethylammonium chloride and acrylic acid (such as polyquatemium 22).
For copolymer of diallyldimethylammonium chloride and acrylic acid the preferred ratio of diallyldimethylammonium chloride to acrylic acid is between approximately 90:10 and 50:50.
The preferred cationic polymer is a copolymer of diallyldimethylammonium chloride and acrylic acid at a 65/35 mole ratio with a molecular weight of approximately 450,000.
The copolymer of diallyldimethylammonium chloride and acrylic acid may be further described by the nomenclature Polyquaternium-22 or PQ22 as named under the International Nomenclature for Cosmetic Ingredients. Copolymers of acrylamide and diallyldimethylammonium chloride may be further described by the nomenclature Polyquatemium-7 or PQ7 as named under the International Nomenclature for Cosmetic Ingredients.
Table 1 below includes cationic charge densities and monomer molecular weights for selected cationic polymers.
Polymer Chemical description Monomer Cationic Charge mw charges density per repeat (meq/g) unit Polyquatemium 22, copolymer of 161.67 30 2.17 neutralized di allyl dim ethyl amm onium (DADMAC) chloride and acrylic acid 65/35 mole ratio, neutralized 94.05 with NaOH (acrylic acid, sodium neutralized) Polyquatemium 22, copolymer of 161.67 65 4.99 un-neutralized di al lyl dim ethyl amm onium (DADMAC) chloride and acrylic acid 65/35 mole ratio 72.06 (acrylic acid) The cationic polymer can be present at a level of from 0.1 % to 10 %, preferably 0.5 % to 5.0 %, more preferably from 1.0 % to 2.5 % by weight of the composition.
For copolymer of diallyldimethylammonium chloride and acrylic acid the preferred ratio of diallyldimethylammonium chloride to acrylic acid is between approximately 90:10 and 50:50.
The preferred cationic polymer is a copolymer of diallyldimethylammonium chloride and acrylic acid at a 65/35 mole ratio with a molecular weight of approximately 450,000.
The copolymer of diallyldimethylammonium chloride and acrylic acid may be further described by the nomenclature Polyquaternium-22 or PQ22 as named under the International Nomenclature for Cosmetic Ingredients. Copolymers of acrylamide and diallyldimethylammonium chloride may be further described by the nomenclature Polyquatemium-7 or PQ7 as named under the International Nomenclature for Cosmetic Ingredients.
Table 1 below includes cationic charge densities and monomer molecular weights for selected cationic polymers.
Polymer Chemical description Monomer Cationic Charge mw charges density per repeat (meq/g) unit Polyquatemium 22, copolymer of 161.67 30 2.17 neutralized di allyl dim ethyl amm onium (DADMAC) chloride and acrylic acid 65/35 mole ratio, neutralized 94.05 with NaOH (acrylic acid, sodium neutralized) Polyquatemium 22, copolymer of 161.67 65 4.99 un-neutralized di al lyl dim ethyl amm onium (DADMAC) chloride and acrylic acid 65/35 mole ratio 72.06 (acrylic acid) The cationic polymer can be present at a level of from 0.1 % to 10 %, preferably 0.5 % to 5.0 %, more preferably from 1.0 % to 2.5 % by weight of the composition.
6 The cationic polymer has a molecular weight of from 1,000 Da to 1,250,000 Da, preferably from 100,000 Da to 1,000,000 Da, more preferably from 250,000 Da to 750,000 Da.
The cationic polymer can have a charge density in the range of 0.05 to 25 meq/g when calculated at pH 7. Without being bound by theory, the molecular weight, charge density, and presence of hydrophobic units within the polymer structure of the cationic polymer may affect the ability of the shielding salt to effectively prevent the polymer-surfactant complex from forming.
Moreover, the charge density may be in the range of 0.05 to 25 meq/g when calculated at pH 7, or preferably below 7.0 meq/g, more preferably below 5.0 meq/g, and even more preferably below 3.0 meq/g when calculated at pH 7. As used herein, "charge density"
refers to the charge density of the final polymer and may be different from the monomer feedstock.
Charge density may be calculated by dividing the number of net charges per repeating unit by the molecular weight of the repeating unit and then multiplying by 1000. It should be noted that the positive charges may be located on the backbone of the cationic polymer and/or on the side chains of the cationic polymer. In the case of cationic polymers with amine monomers, the charge density depends on the pH of the carrier and thus the charge density for comparison with this disclosure should be measured at pH of 7.
Surfactant system The laundry composition comprises a surfactant system at a level of from 2.5 %
to 60 %, preferably from 5.0 % to 25 %, more preferably from 7.0 % to 15 % by weight of the composition.
Suitable surfactants as used herein means surfactants or mixtures of surfactants that provide cleaning, stain removing, or laundering benefit to soiled material. Suitable detersive surfactants can be: anionic surfactant, nonionic surfactant, zwitterionic surfactant, and combinations thereof.
The surfactant system comprises branched nonionic surfactant. The surfactant system can further comprise a surfactant selected from the group consisting of: anionic surfactant, amphoteric surfactant, and mixtures thereof. As such, the surfactant system can comprise a combination of anionic and nonionic surfactant, more preferably a combination of anionic surfactant, nonionic surfactant, and amphoteric surfactant.
Preferably surfactants comprising saturated alkyl chains are used.
Branched nonionic surfactant The surfactant system can comprise branched nonionic surfactant at a level of from 0.1% to 12%, preferably from 0.5% to 10%, more preferably from 1.0% to 3.0% by weight of the composition.
The cationic polymer can have a charge density in the range of 0.05 to 25 meq/g when calculated at pH 7. Without being bound by theory, the molecular weight, charge density, and presence of hydrophobic units within the polymer structure of the cationic polymer may affect the ability of the shielding salt to effectively prevent the polymer-surfactant complex from forming.
Moreover, the charge density may be in the range of 0.05 to 25 meq/g when calculated at pH 7, or preferably below 7.0 meq/g, more preferably below 5.0 meq/g, and even more preferably below 3.0 meq/g when calculated at pH 7. As used herein, "charge density"
refers to the charge density of the final polymer and may be different from the monomer feedstock.
Charge density may be calculated by dividing the number of net charges per repeating unit by the molecular weight of the repeating unit and then multiplying by 1000. It should be noted that the positive charges may be located on the backbone of the cationic polymer and/or on the side chains of the cationic polymer. In the case of cationic polymers with amine monomers, the charge density depends on the pH of the carrier and thus the charge density for comparison with this disclosure should be measured at pH of 7.
Surfactant system The laundry composition comprises a surfactant system at a level of from 2.5 %
to 60 %, preferably from 5.0 % to 25 %, more preferably from 7.0 % to 15 % by weight of the composition.
Suitable surfactants as used herein means surfactants or mixtures of surfactants that provide cleaning, stain removing, or laundering benefit to soiled material. Suitable detersive surfactants can be: anionic surfactant, nonionic surfactant, zwitterionic surfactant, and combinations thereof.
The surfactant system comprises branched nonionic surfactant. The surfactant system can further comprise a surfactant selected from the group consisting of: anionic surfactant, amphoteric surfactant, and mixtures thereof. As such, the surfactant system can comprise a combination of anionic and nonionic surfactant, more preferably a combination of anionic surfactant, nonionic surfactant, and amphoteric surfactant.
Preferably surfactants comprising saturated alkyl chains are used.
Branched nonionic surfactant The surfactant system can comprise branched nonionic surfactant at a level of from 0.1% to 12%, preferably from 0.5% to 10%, more preferably from 1.0% to 3.0% by weight of the composition.
7 Suitable branched nonionic surfactants can be derived from primary or secondary alcohols.
The branched nonionic surfactant are selected from:
a) Formula I: R1-CH(R2)-0-(P0)(E0)y(P0)z-H
In Formula I, R1 is a C4 to C14 alkyl chain, preferably C4 to C8, more preferably C6; R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain; x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3; y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12; and z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, E0 stands for ethoxylati on and PO stands for propoxylati on;
b) Formula II: R1-CH(R2)CH2-0-(P0)x(E0)y(P0)z-H
Tn formula TT: R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5; R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain; x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3; y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12; and z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, EO stands for ethoxylation and PO stands for propoxylation.
Preferred branched non-ionic ethoxylates according to formula I are those available under the tradenames Tergitol 15-S, with an alkoxylation degree of from 3 to 40.
For instance Tergitol 15-S-20 which has an average degree of alkoxylation of 20. Other suitable commercially available material according to formula I are the ones available under the tradename Softanol M and EP
series.
Preferred branched nonionic surfactants according to formula II are the Guerbet C10 alcohol ethoxylates with 7 or 8 E0, such as Ethylae 1007 & 1008, and the Guerbet C10 alcohol alkoxylated nonionic surfactants (which are ethoxylated and/or propoxylated) such as the commercially available Lutensol XL series (XL50, XL70. etc). Other exemplary alkoxylated branched nonionic surfactants include those available under the trade names:
Lutensol XP30, Lutensol XP-50, and Lutensol XP-80 available from BASF Corporation. In general, Lutensol XP-30 can be considered to have 3 repeating ethoxy groups, Lutensol XP-50 can be considered to have 5 repeating ethoxy groups, and Lutensol XP-70 can be considered to have 7 repeating ethoxy groups. Other suitable branched nonionic surfactants include oxo branched nonionic surfactants such as the Lutensol ON 50 (5 EO) and Lutensol 0N70 (7 EO).
Other suitable branched nonionic surfactants include Plurafac SLF 170 (3P0, 12E0, 15P0).
Also suitable are:
the ethoxylated fatty alcohols originating from the Fischer & Tropsch reaction comprising up to 50% branching (40% methyl (mono or bi), 10% cyclohexyl) such as those produced from the
The branched nonionic surfactant are selected from:
a) Formula I: R1-CH(R2)-0-(P0)(E0)y(P0)z-H
In Formula I, R1 is a C4 to C14 alkyl chain, preferably C4 to C8, more preferably C6; R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain; x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3; y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12; and z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, E0 stands for ethoxylati on and PO stands for propoxylati on;
b) Formula II: R1-CH(R2)CH2-0-(P0)x(E0)y(P0)z-H
Tn formula TT: R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5; R2 is a Cl to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain; x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3; y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12; and z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3, EO stands for ethoxylation and PO stands for propoxylation.
Preferred branched non-ionic ethoxylates according to formula I are those available under the tradenames Tergitol 15-S, with an alkoxylation degree of from 3 to 40.
For instance Tergitol 15-S-20 which has an average degree of alkoxylation of 20. Other suitable commercially available material according to formula I are the ones available under the tradename Softanol M and EP
series.
Preferred branched nonionic surfactants according to formula II are the Guerbet C10 alcohol ethoxylates with 7 or 8 E0, such as Ethylae 1007 & 1008, and the Guerbet C10 alcohol alkoxylated nonionic surfactants (which are ethoxylated and/or propoxylated) such as the commercially available Lutensol XL series (XL50, XL70. etc). Other exemplary alkoxylated branched nonionic surfactants include those available under the trade names:
Lutensol XP30, Lutensol XP-50, and Lutensol XP-80 available from BASF Corporation. In general, Lutensol XP-30 can be considered to have 3 repeating ethoxy groups, Lutensol XP-50 can be considered to have 5 repeating ethoxy groups, and Lutensol XP-70 can be considered to have 7 repeating ethoxy groups. Other suitable branched nonionic surfactants include oxo branched nonionic surfactants such as the Lutensol ON 50 (5 EO) and Lutensol 0N70 (7 EO).
Other suitable branched nonionic surfactants include Plurafac SLF 170 (3P0, 12E0, 15P0).
Also suitable are:
the ethoxylated fatty alcohols originating from the Fischer & Tropsch reaction comprising up to 50% branching (40% methyl (mono or bi), 10% cyclohexyl) such as those produced from the
8 Safol alcohols from Sasol; ethoxylated fatty alcohols originating from the oxo reaction wherein at least 50 % by weight of the alcohol is C2 isomer (methyl to pentyl) such as those produced from the Isalchem alcohols or Lial alcohols from Sasol.
Further nonionic surfactant The liquid detergent composition can comprise further nonionic surfactant. The level of further nonionic surfactant in the liquid detergent composition can be present at a level of less than wt%, preferably less than 7.0 wt%, more preferably less than 5.0 wt%, and even more preferably less than 3.0 wt %. Most preferably, the composition is free of further nonionic surfactant.
Suitable nonionic surfactants include, but are not limited to linear C12-C18 alkyl ethoxylates ("AE") including the so-called narrow peaked alkyl ethoxylates and C6-C12 alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxy/propoxy), block alkylene oxide condensate of C6-C12 alkyl phenols, alkylene oxide condensates of C8-C22 alkanols and ethylene oxide/propylene oxide block polymers (Pluronic - BASF Corp.), as well as semi polar nonionics (e.g., amine oxides and phosphine oxides) can be used in the present compositions. An extensive disclosure of these types of surfactants is found in U.S. Pat. 3,929,678.
Alkylpolysaccharides such as disclosed in U.S. Pat. 4,565,647 are also useful nonionic surfactants in the compositions of the invention.
Also suitable are alkyl polyglucoside surfactants.
Further nonionic surfactants of use include those of the formula Ri(OC2H4).0H, wherein Ri is a linear C10-C16 alkyl group or a C8-C12 alkyl phenyl group, and n is from preferably 3 to 80. In some embodiments, the nonionic surfactants may be condensation products of linear C12-C15 alcohols with from 5 to 20 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with 6.5 moles of ethylene oxide per mole of alcohol Anionic surfactant The surfactant system can comprise anionic surfactant at a level of from 1.4%
to 52%, preferably from 4.4% to 20%, more preferably from 5.9% to 11.5% of the liquid laundry detergent composition.
The surfactant system can further comprise an anionic surfactant, preferably selected from the group consisting of: sulphonate surfactant, sulphate surfactant, and mixtures thereof, more preferably wherein the anionic surfactant comprises sulphonate surfactant and sulphate surfactant.
Suitable anionic surfactants also include fatty acids and their salts, which are typically added as
Further nonionic surfactant The liquid detergent composition can comprise further nonionic surfactant. The level of further nonionic surfactant in the liquid detergent composition can be present at a level of less than wt%, preferably less than 7.0 wt%, more preferably less than 5.0 wt%, and even more preferably less than 3.0 wt %. Most preferably, the composition is free of further nonionic surfactant.
Suitable nonionic surfactants include, but are not limited to linear C12-C18 alkyl ethoxylates ("AE") including the so-called narrow peaked alkyl ethoxylates and C6-C12 alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxy/propoxy), block alkylene oxide condensate of C6-C12 alkyl phenols, alkylene oxide condensates of C8-C22 alkanols and ethylene oxide/propylene oxide block polymers (Pluronic - BASF Corp.), as well as semi polar nonionics (e.g., amine oxides and phosphine oxides) can be used in the present compositions. An extensive disclosure of these types of surfactants is found in U.S. Pat. 3,929,678.
Alkylpolysaccharides such as disclosed in U.S. Pat. 4,565,647 are also useful nonionic surfactants in the compositions of the invention.
Also suitable are alkyl polyglucoside surfactants.
Further nonionic surfactants of use include those of the formula Ri(OC2H4).0H, wherein Ri is a linear C10-C16 alkyl group or a C8-C12 alkyl phenyl group, and n is from preferably 3 to 80. In some embodiments, the nonionic surfactants may be condensation products of linear C12-C15 alcohols with from 5 to 20 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with 6.5 moles of ethylene oxide per mole of alcohol Anionic surfactant The surfactant system can comprise anionic surfactant at a level of from 1.4%
to 52%, preferably from 4.4% to 20%, more preferably from 5.9% to 11.5% of the liquid laundry detergent composition.
The surfactant system can further comprise an anionic surfactant, preferably selected from the group consisting of: sulphonate surfactant, sulphate surfactant, and mixtures thereof, more preferably wherein the anionic surfactant comprises sulphonate surfactant and sulphate surfactant.
Suitable anionic surfactants also include fatty acids and their salts, which are typically added as
9 builders. However, by nature, every anionic surfactant known in the art of detergent compositions may be used, such as disclosed in "Surfactant Science Series", Vol. 7, edited by W. M. Linfield, Marcel Dekker. However, the composition preferably comprises at least a sulphonic acid surfactant, such as a linear alkyl benzene sulphonic acid, but water-soluble salt forms may also be used. Alkyl sulphates, or mixtures thereof, are also preferred. A combination of linear alkyl benzene sulphonate and alkyl sulphate surfactant is particularly preferred, especially for improving stain removal.
Anionic sulphonate or sulphonic acid surfactants suitable for use herein include the acid and salt forms of alkylbenzene sulphonates, alkyl ester sulphonates, alkane sulphonates, alkyl sulphonated polycarboxylic acids, and mixtures thereof Suitable anionic sulphonate or sulphonic acid surfactants include: C5-C20 alkylbenzene sulphonates, more preferably C10-alkylbenzene sulphonates, more preferably C11-C13 alkylbenzene sulphonates, C5-C20 alkyl ester sulphonates, C6-C22 primary or secondary alkane sulphonates, C5-C20 sulphonated polycarboxylic acids, and any mixtures thereof, but preferably Cl 1-C13 alkylbenzene sulphonates.
The aforementioned surfactants can vary widely in their 2-phenyl isomer content.
Anionic sulphate salts suitable for use in the compositions of the invention include the primary and secondary alkyl sulphates, having a linear or branched alkyl or alkenyl moiety having from 9 to 22 carbon atoms or more preferably 12 to18 carbon atoms. Also useful are beta-branched alkyl sulphate surfactants or mixtures of commercially available materials, having a weight average (of the surfactant or the mixture) branching degree of at least 50%.
Mid-chain branched alkyl sulphates or sulphonates are also suitable anionic surfactants for use in the compositions of the invention. Preferred are the C5-C22, preferably C10-C20 mid-chain branched alkyl primary sulphates. When mixtures are used, a suitable average total number of carbon atoms for the alkyl moieties is preferably within the range of from greater than 14.5 to 17.5.
Preferred mono-methyl-branched primary alkyl sulphates are selected from the group consisting of the 3-methyl to 13-methyl pentadecanol sulphates, the corresponding hexadecanol sulphates, and mixtures thereof. Dimethyl derivatives or other biodegradable alkyl sulphates having light branching can similarly be used.
When used, the alkyl alkoxylated sulphate surfactant can be a blend of one or more alkyl ethoxylated sulphates. Suitable alkyl alkoxylated sulphates include C 1 0-C18 alkyl ethoxylated sulphates, more preferably C12-C15 alkyl ethoxylated sulphates. The anionic surfactant can comprise alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has an average degree of ethoxylation of from 0.5 to 8.0, preferably from 1.0 to 5.0, more preferably from 2.0 to 3.5.
Alternatively, the anionic surfactant can comprise alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has a low degree of ethoxylation, having an average degree of ethoxylation of less than 0.5, preferably less than 0.1, and more preferably is free of ethoxylation.
Preferred low ethoxylation alkyl sulphate surfactants do not comprise any further alkoxylation.
5 Preferred low ethoxylation alkyl sulphate surfactants comprise branched alkyl sulphate surfactant.
The branched alkyl sulphate surfactant can comprise at least 20%, preferably from 60% to 100%, more preferably from 80% to 90% by weight of the alkyl chains of the branched alkyl sulphate surfactant of 2-branched alkyl chains. Such branched alkyl sulphates with 2-branched alkyl chains can also be described as 2-alkyl alkanol sulphates, or 2-alkyl alkyl sulphates. The branched alkyl
Anionic sulphonate or sulphonic acid surfactants suitable for use herein include the acid and salt forms of alkylbenzene sulphonates, alkyl ester sulphonates, alkane sulphonates, alkyl sulphonated polycarboxylic acids, and mixtures thereof Suitable anionic sulphonate or sulphonic acid surfactants include: C5-C20 alkylbenzene sulphonates, more preferably C10-alkylbenzene sulphonates, more preferably C11-C13 alkylbenzene sulphonates, C5-C20 alkyl ester sulphonates, C6-C22 primary or secondary alkane sulphonates, C5-C20 sulphonated polycarboxylic acids, and any mixtures thereof, but preferably Cl 1-C13 alkylbenzene sulphonates.
The aforementioned surfactants can vary widely in their 2-phenyl isomer content.
Anionic sulphate salts suitable for use in the compositions of the invention include the primary and secondary alkyl sulphates, having a linear or branched alkyl or alkenyl moiety having from 9 to 22 carbon atoms or more preferably 12 to18 carbon atoms. Also useful are beta-branched alkyl sulphate surfactants or mixtures of commercially available materials, having a weight average (of the surfactant or the mixture) branching degree of at least 50%.
Mid-chain branched alkyl sulphates or sulphonates are also suitable anionic surfactants for use in the compositions of the invention. Preferred are the C5-C22, preferably C10-C20 mid-chain branched alkyl primary sulphates. When mixtures are used, a suitable average total number of carbon atoms for the alkyl moieties is preferably within the range of from greater than 14.5 to 17.5.
Preferred mono-methyl-branched primary alkyl sulphates are selected from the group consisting of the 3-methyl to 13-methyl pentadecanol sulphates, the corresponding hexadecanol sulphates, and mixtures thereof. Dimethyl derivatives or other biodegradable alkyl sulphates having light branching can similarly be used.
When used, the alkyl alkoxylated sulphate surfactant can be a blend of one or more alkyl ethoxylated sulphates. Suitable alkyl alkoxylated sulphates include C 1 0-C18 alkyl ethoxylated sulphates, more preferably C12-C15 alkyl ethoxylated sulphates. The anionic surfactant can comprise alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has an average degree of ethoxylation of from 0.5 to 8.0, preferably from 1.0 to 5.0, more preferably from 2.0 to 3.5.
Alternatively, the anionic surfactant can comprise alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has a low degree of ethoxylation, having an average degree of ethoxylation of less than 0.5, preferably less than 0.1, and more preferably is free of ethoxylation.
Preferred low ethoxylation alkyl sulphate surfactants do not comprise any further alkoxylation.
5 Preferred low ethoxylation alkyl sulphate surfactants comprise branched alkyl sulphate surfactant.
The branched alkyl sulphate surfactant can comprise at least 20%, preferably from 60% to 100%, more preferably from 80% to 90% by weight of the alkyl chains of the branched alkyl sulphate surfactant of 2-branched alkyl chains. Such branched alkyl sulphates with 2-branched alkyl chains can also be described as 2-alkyl alkanol sulphates, or 2-alkyl alkyl sulphates. The branched alkyl
10 sulphates can be neutralized by sodium, potassium, magnesium, lithium, calcium, ammonium, or any suitable amines, such as, but not limited to monoethanolamine, triethanolamine and monoisopropanolamine, or by mixtures of any of the neutralizing metals or amines. Suitable branched alkyl sulphate surfactants can comprise alkyl chains comprising from 10 to 18 carbon atoms (C10 to C18) or from 12 to 15 carbon atoms (C12 to C15), with 13 to 15 carbon atoms (C13 to C15) being most preferred. The branched alkyl sulphate surfactant can be produced using processes which comprise a hydroformylation reaction in order to provide the desired levels of 2-branching. Particularly preferred branched alkyl sulphate surfactants comprise 2-branching, wherein the 2-branching comprises from 20% to 80%, preferably from 30% to 65%, more preferably from 40% to 50% by weight of the 2-branching of methyl branching, ethyl branching, and mixtures thereof.
Suitable low ethoxylated branched alkyl sulphate surfactants can be derived from alkyl alcohols such as Lial 145, Isalchem 145, both supplied by Sasol, optionally blending with other alkyl alcohols in order to achieve the desired branching distributions.
Lower levels of dye removal from fabrics during laundering can be achieved while maintaining cleaning performance, when laundering the fabrics at temperatures of 30 C or below when the fabrics are washed using compositions of the present invention comprising such low ethoxylated alkyl sulphate surfactants, especially when the low ethoxylated alkyl sulphate surfactants comprise the 2-branching as described above Processes to make such alkyl ether sulphate anionic surfactants may result in trace residual amounts of 1,4-dioxane by-product being present. The amount of 1,4-dioxane by-product within alkoxylated especially ethoxylated alkyl sulphates can be reduced. Based on recent advances in technology, a further reduction of 1,4-dioxane by-product can be achieved by subsequent stripping, distillation, evaporation, centrifugation, microwave irradiation, molecular sieving or
Suitable low ethoxylated branched alkyl sulphate surfactants can be derived from alkyl alcohols such as Lial 145, Isalchem 145, both supplied by Sasol, optionally blending with other alkyl alcohols in order to achieve the desired branching distributions.
Lower levels of dye removal from fabrics during laundering can be achieved while maintaining cleaning performance, when laundering the fabrics at temperatures of 30 C or below when the fabrics are washed using compositions of the present invention comprising such low ethoxylated alkyl sulphate surfactants, especially when the low ethoxylated alkyl sulphate surfactants comprise the 2-branching as described above Processes to make such alkyl ether sulphate anionic surfactants may result in trace residual amounts of 1,4-dioxane by-product being present. The amount of 1,4-dioxane by-product within alkoxylated especially ethoxylated alkyl sulphates can be reduced. Based on recent advances in technology, a further reduction of 1,4-dioxane by-product can be achieved by subsequent stripping, distillation, evaporation, centrifugation, microwave irradiation, molecular sieving or
11 catalytic or enzymatic degradation steps. An alternative is to use alkyl sulphate anionic surfactants which comprise only low levels of ethoxylation, or even being free of ethoxylation. As such, the alkyl sulphate surfactant can have a degree of ethoxylation of less than 1.0, or less than 0.5, or even be free of ethoxylation.
Other suitable anionic surfactants for use herein include fatty methyl ester sulphonates and/or alkyl polyalkoxylated carboxylates, for example, alkyl ethoxylated carboxylates (AEC).
The anionic surfactants are typically present in the form of their salts with alkanolamines or alkali metals such as sodium and potassium.
For improved stability and grease cleaning, the liquid detergent composition can comprise a combination of linear alkyl benzene sulphonate surfactant and alkyl sulphate surfactant, preferably such that the ratio of linear alkyl benzene sulphonate surfactant to alkyl alkoxylated sulphate surfactant is from 15:1 to 0.1:1 ,preferably from 10:1 to 0.3:1 ,more preferably from 5:1 to 1:1.
Amphoteric and/or zwitterionic surfactant The surfactant system can comprise amphoteric amid/or zwitterionic surfactant at a level of from 0.1% to 2.0%, preferably from 0.1% to 1.0%, more preferably from 0.1% to 0.5% by weight of the liquid laundry detergent composition.
Suitable amphoteric surfactants include amine oxide surfactants. Amine oxide surfactants are amine oxides having the following formula : R1R7R3NO wherein R1 is an hydrocarbon chain comprising from 1 to 30 carbon atoms, preferably from 6 to 20, more preferably from 8 to 16 and wherein R2 and R3 are independently saturated or unsaturated, substituted or unsubstituted, linear or branched hydrocarbon chains comprising from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups. R1 may be a saturated or unsaturated, substituted or unsubstituted linear or branched hydrocarbon chain.
Suitable amine oxides for use herein are for instance preferably C12-C14 dimethyl amine oxide (lauryl dimethylamine oxide), commercially available from Albright &
Wilson, C12-C14 amine oxides commercially available under the trade name Genaminox LA from Clariant or AROMOX DMC from AKZO Nobel.
Suitable amphoteric or zwitterionic detersive surfactants include those which are known for use in hair care or other personal care cleansing. Non-limiting examples of suitable zwitterionic or amphoteric surfactants are described in U.S. Pat. Nos. 5,104,646, 5,106,609. Suitable
Other suitable anionic surfactants for use herein include fatty methyl ester sulphonates and/or alkyl polyalkoxylated carboxylates, for example, alkyl ethoxylated carboxylates (AEC).
The anionic surfactants are typically present in the form of their salts with alkanolamines or alkali metals such as sodium and potassium.
For improved stability and grease cleaning, the liquid detergent composition can comprise a combination of linear alkyl benzene sulphonate surfactant and alkyl sulphate surfactant, preferably such that the ratio of linear alkyl benzene sulphonate surfactant to alkyl alkoxylated sulphate surfactant is from 15:1 to 0.1:1 ,preferably from 10:1 to 0.3:1 ,more preferably from 5:1 to 1:1.
Amphoteric and/or zwitterionic surfactant The surfactant system can comprise amphoteric amid/or zwitterionic surfactant at a level of from 0.1% to 2.0%, preferably from 0.1% to 1.0%, more preferably from 0.1% to 0.5% by weight of the liquid laundry detergent composition.
Suitable amphoteric surfactants include amine oxide surfactants. Amine oxide surfactants are amine oxides having the following formula : R1R7R3NO wherein R1 is an hydrocarbon chain comprising from 1 to 30 carbon atoms, preferably from 6 to 20, more preferably from 8 to 16 and wherein R2 and R3 are independently saturated or unsaturated, substituted or unsubstituted, linear or branched hydrocarbon chains comprising from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups. R1 may be a saturated or unsaturated, substituted or unsubstituted linear or branched hydrocarbon chain.
Suitable amine oxides for use herein are for instance preferably C12-C14 dimethyl amine oxide (lauryl dimethylamine oxide), commercially available from Albright &
Wilson, C12-C14 amine oxides commercially available under the trade name Genaminox LA from Clariant or AROMOX DMC from AKZO Nobel.
Suitable amphoteric or zwitterionic detersive surfactants include those which are known for use in hair care or other personal care cleansing. Non-limiting examples of suitable zwitterionic or amphoteric surfactants are described in U.S. Pat. Nos. 5,104,646, 5,106,609. Suitable
12 amphoteric detersive surfactants include those surfactants broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight or branched chain and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulphonate, sulphate, phosphate, or phosphonate.
Suitable amphoteric detersive surfactants for use in the present invention include, but are not limited to: cocoamphoacetate, cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixtures thereof.
Optional Ingredients The detergent composition may additionally comprise one or more of the following optional ingredients: external structurant or thickener, enzymes, enzyme stabilizers, cleaning polymers, bleaching systems, optical brighteners, hueing dyes, particulate material, perfume and other odour control agents, hydrotropes, suds suppressors, fabric care benefit agents, pH adjusting agents, dye transfer inhibiting agents, dye fixative polymers, preservatives, non-fabric substantive dyes and mixtures thereof In more preferred embodiments, the laundry detergent composition does not comprise a bleach.
External structurant or thickener: Preferred external structurants and thickeners are those that do not rely on charge ¨ charge interactions for providing a structuring benefit. As such, particularly preferred external structurants are uncharged external structurants, such as those selected from the group consisting of: non-polymeric crystalline, hydroxyl functional structurants, such as hydrogenated castor oil; microfibrillated cellulose; uncharged hydroxyethyl cellulose;
uncharged hydrophobically modified hydroxyethyl cellulose; hydrophobically modified ethoxylated urethanes; hydrophobically modified non-ionic polyols; and mixtures thereof.
Suitable polymeric structurants include naturally derived and/or synthetic polymeric structurants.
Examples of naturally derived polymeric structurants of use in the present invention include: microfibrillated cellulose, hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose, polysaccharide derivatives and mixtures thereof.
Non-limiting examples of microfibrillated cellulose are described in WO
2009/101545 Al.
Suitable polysaccharide derivatives include: pectine, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, xanthan gum, guar gum and mixtures thereof Examples of synthetic polymeric structurants or thickeners of use in the present invention include: polycarboxyl ates, hydrophobi cal 1 y modified ethoxyl ated urethanes (TIEUr),
Suitable amphoteric detersive surfactants for use in the present invention include, but are not limited to: cocoamphoacetate, cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixtures thereof.
Optional Ingredients The detergent composition may additionally comprise one or more of the following optional ingredients: external structurant or thickener, enzymes, enzyme stabilizers, cleaning polymers, bleaching systems, optical brighteners, hueing dyes, particulate material, perfume and other odour control agents, hydrotropes, suds suppressors, fabric care benefit agents, pH adjusting agents, dye transfer inhibiting agents, dye fixative polymers, preservatives, non-fabric substantive dyes and mixtures thereof In more preferred embodiments, the laundry detergent composition does not comprise a bleach.
External structurant or thickener: Preferred external structurants and thickeners are those that do not rely on charge ¨ charge interactions for providing a structuring benefit. As such, particularly preferred external structurants are uncharged external structurants, such as those selected from the group consisting of: non-polymeric crystalline, hydroxyl functional structurants, such as hydrogenated castor oil; microfibrillated cellulose; uncharged hydroxyethyl cellulose;
uncharged hydrophobically modified hydroxyethyl cellulose; hydrophobically modified ethoxylated urethanes; hydrophobically modified non-ionic polyols; and mixtures thereof.
Suitable polymeric structurants include naturally derived and/or synthetic polymeric structurants.
Examples of naturally derived polymeric structurants of use in the present invention include: microfibrillated cellulose, hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose, polysaccharide derivatives and mixtures thereof.
Non-limiting examples of microfibrillated cellulose are described in WO
2009/101545 Al.
Suitable polysaccharide derivatives include: pectine, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, xanthan gum, guar gum and mixtures thereof Examples of synthetic polymeric structurants or thickeners of use in the present invention include: polycarboxyl ates, hydrophobi cal 1 y modified ethoxyl ated urethanes (TIEUr),
13 hydrophobically modified non-ionic polyols and mixtures thereof.
Preferably, the aqueous liquid detergent composition has a viscosity of 50 to 5,000, preferably 75 to 1,000, more preferably 100 to 500 mPa.s, when measured at a shear rate of 100 s-1, at a temperature of 20 C. For improved phase stability, and also improved stability of suspended ingredients, the aqueous liquid detergent composition has a viscosity of 50 to 250,000, preferably 5,000 to 125,000, more preferably 10,000 to 35,000 mPa.s, when measured at a shear rate of 0.05 s-1, at a temperature of 20 C.
Cleaning polymers: The detergent composition preferably comprises a cleaning polymer.
Such cleaning polymers are believed to at least partially lift the stain from the textile fibres and enable the enzyme system to more effectively break up the complexes comprising mannan and other polysaccharide. Suitable cleaning polymers provide for broad-range soil cleaning of surfaces and fabrics and/or suspension of the soils. Non-limiting examples of suitable cleaning polymers include: amphiphilic alkoxylated grease cleaning polymers; clay soil cleaning polymers; soil release polymers; and soil suspending polymers. A preferred cleaning polymer is obtainable by free-radical copolymerization of at least one compound of formula (I), (I) n in which n is equal to or greater than 3 for a number, with at least one compound of formula (II), (II) in which A- represents an anion, in particular selected from halides such as fluoride, chloride, bromide, iodide, sulphate, hydrogen sulphate, alkyl sulphate such as methyl sulphate, and mixtures thereof. Such polymers are further described in EP3196283A1.
For similar reasons, polyester based soil release polymers, such as SRA300, supplied by Clariant are also particularly preferred.
Other useful cleaning polymers are described in U520090124528A1. The detergent composition may comprise amphiphilic alkoxylated grease cleaning polymers, which may have balanced hydrophilic and hydrophobic properties such that they remove grease particles from
Preferably, the aqueous liquid detergent composition has a viscosity of 50 to 5,000, preferably 75 to 1,000, more preferably 100 to 500 mPa.s, when measured at a shear rate of 100 s-1, at a temperature of 20 C. For improved phase stability, and also improved stability of suspended ingredients, the aqueous liquid detergent composition has a viscosity of 50 to 250,000, preferably 5,000 to 125,000, more preferably 10,000 to 35,000 mPa.s, when measured at a shear rate of 0.05 s-1, at a temperature of 20 C.
Cleaning polymers: The detergent composition preferably comprises a cleaning polymer.
Such cleaning polymers are believed to at least partially lift the stain from the textile fibres and enable the enzyme system to more effectively break up the complexes comprising mannan and other polysaccharide. Suitable cleaning polymers provide for broad-range soil cleaning of surfaces and fabrics and/or suspension of the soils. Non-limiting examples of suitable cleaning polymers include: amphiphilic alkoxylated grease cleaning polymers; clay soil cleaning polymers; soil release polymers; and soil suspending polymers. A preferred cleaning polymer is obtainable by free-radical copolymerization of at least one compound of formula (I), (I) n in which n is equal to or greater than 3 for a number, with at least one compound of formula (II), (II) in which A- represents an anion, in particular selected from halides such as fluoride, chloride, bromide, iodide, sulphate, hydrogen sulphate, alkyl sulphate such as methyl sulphate, and mixtures thereof. Such polymers are further described in EP3196283A1.
For similar reasons, polyester based soil release polymers, such as SRA300, supplied by Clariant are also particularly preferred.
Other useful cleaning polymers are described in U520090124528A1. The detergent composition may comprise amphiphilic alkoxylated grease cleaning polymers, which may have balanced hydrophilic and hydrophobic properties such that they remove grease particles from
14 fabrics and surfaces. The amphiphilic alkoxylated grease cleaning polymers may comprise a core structure and a plurality of alkoxylate groups attached to that core structure. These may comprise alkoxylated polyalkyleneimines, for example. Such compounds may comprise, but are not limited to, ethoxylated polyethyleneimine, ethoxylated hexamethylene diamine, and sulphated versions thereof. Polypropoxylated derivatives may also be included. A wide variety of amines and polyalklyeneimines can be alkoxylated to various degrees. A useful example is 600g/mol polyethyleneimine core ethoxylated to 20 EO groups per NH and is available from BASF. The alkoxylated polyalkyleneimines may have an inner polyethylene oxide block and an outer polypropylene oxide block. The detergent compositions may comprise from 0.1%
to 10%, preferably, from 0.1% to 8.0%, more preferably from 0,1% to 2.0%, by weight of the detergent composition, of the cleaning polymer.
Dye transfer inhibiting polymers: The detergent composition can comprise one or more dye transfer inhibiting polymer. However, preferred compositions do not comprise such dye transfer inhibiting polymers. It has been found that during laundering, many fabric-dyes partition between the fabric and wash-liquor. As such, the sequestering of dyes in the wash liquor using DTI polymers has been found to increase dye removal from fabrics, and hence increase dye-fading.
When used, suitable dye transfer inhibiting can be selected from the group consisting of polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), polyvinyl pyridine-N-oxide, poly-N-carboxymethy1-4-vinylpyridiumchloride, poly(2-hydroxypropyldimethylammonium chloride), and mixtures thereof, preferably polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), and mixtures thereof. If present, the dye transfer inhibitor can be present at a level of from 0.05% to 5%, or from 0.1% to 3%, and or from 0.2% to 2.5%, by weight of the detergent composition.
Polyvinylpyrrolidone ("PVP") has an amphiphilic character with a highly polar amide group conferring hydrophilic and polar attracting properties, and also has apolar methylene and methane groups, in the backbone and/or the ring, conferring hydrophobic properties. The rings may also provide planar alignment with the aromatic rings, in the dye molecules. PVP is readily soluble in aqueous and organic solvent systems PVP is commercially available in either powder or aqueous solutions in several viscosity grades. The compositions of the present invention preferably utilize a copolymer of N- vinylpyrrolidone and N-vinylimidazole (also abbreviated herein as "PVPVI"). It has been found that copolymers of N-vinylpyrrolidone and N-vinylimidazole can provide excellent dye transfer inhibiting performance. The copolymers of N-vinylpyrrolidone and N-vinylimidazole can have a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1:1 to 0.2:1, more preferably from 0.8:1 to 0.3:1, most preferably from 0.6:1 to 0.4:1. The copolymer of N-vinylpyrrolidone and N-vinylimidazole can be either linear or branched. Particularly suitable polyvinylpyrrolidones (PVP), polyvinylimidazoles (PVI), and 5 copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), can have a weight average molecular weight of from 5,000 Da to 1,000, 000 Da, preferably from 5,000 Da to 50,000 Da, more preferably from 10,000 Da to 20,000 Da. The number average molecular weight range is determined by light scattering as described in Barth J. H. G. and Mays J. W.
Chemical Analysis Vol 1 13. "Modern Methods of Polymer Characterization." Copolymers of poly (N-vinyl-2-10 pyrollidone) and poly (N-vinyl-imidazole) are commercially available from a number of sources including BASF. A preferred DTI is commercially available under the tradename Sokalang HP
56 K from BASF (BASF SE, Germany).
Organic builder and/or chelant: The laundry detergent composition can comprise from 0.6% to 10%, preferably from 2 to 7% by weight of one or more organic builder and/or chelants.
to 10%, preferably, from 0.1% to 8.0%, more preferably from 0,1% to 2.0%, by weight of the detergent composition, of the cleaning polymer.
Dye transfer inhibiting polymers: The detergent composition can comprise one or more dye transfer inhibiting polymer. However, preferred compositions do not comprise such dye transfer inhibiting polymers. It has been found that during laundering, many fabric-dyes partition between the fabric and wash-liquor. As such, the sequestering of dyes in the wash liquor using DTI polymers has been found to increase dye removal from fabrics, and hence increase dye-fading.
When used, suitable dye transfer inhibiting can be selected from the group consisting of polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), polyvinyl pyridine-N-oxide, poly-N-carboxymethy1-4-vinylpyridiumchloride, poly(2-hydroxypropyldimethylammonium chloride), and mixtures thereof, preferably polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), and mixtures thereof. If present, the dye transfer inhibitor can be present at a level of from 0.05% to 5%, or from 0.1% to 3%, and or from 0.2% to 2.5%, by weight of the detergent composition.
Polyvinylpyrrolidone ("PVP") has an amphiphilic character with a highly polar amide group conferring hydrophilic and polar attracting properties, and also has apolar methylene and methane groups, in the backbone and/or the ring, conferring hydrophobic properties. The rings may also provide planar alignment with the aromatic rings, in the dye molecules. PVP is readily soluble in aqueous and organic solvent systems PVP is commercially available in either powder or aqueous solutions in several viscosity grades. The compositions of the present invention preferably utilize a copolymer of N- vinylpyrrolidone and N-vinylimidazole (also abbreviated herein as "PVPVI"). It has been found that copolymers of N-vinylpyrrolidone and N-vinylimidazole can provide excellent dye transfer inhibiting performance. The copolymers of N-vinylpyrrolidone and N-vinylimidazole can have a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1:1 to 0.2:1, more preferably from 0.8:1 to 0.3:1, most preferably from 0.6:1 to 0.4:1. The copolymer of N-vinylpyrrolidone and N-vinylimidazole can be either linear or branched. Particularly suitable polyvinylpyrrolidones (PVP), polyvinylimidazoles (PVI), and 5 copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), can have a weight average molecular weight of from 5,000 Da to 1,000, 000 Da, preferably from 5,000 Da to 50,000 Da, more preferably from 10,000 Da to 20,000 Da. The number average molecular weight range is determined by light scattering as described in Barth J. H. G. and Mays J. W.
Chemical Analysis Vol 1 13. "Modern Methods of Polymer Characterization." Copolymers of poly (N-vinyl-2-10 pyrollidone) and poly (N-vinyl-imidazole) are commercially available from a number of sources including BASF. A preferred DTI is commercially available under the tradename Sokalang HP
56 K from BASF (BASF SE, Germany).
Organic builder and/or chelant: The laundry detergent composition can comprise from 0.6% to 10%, preferably from 2 to 7% by weight of one or more organic builder and/or chelants.
15 Suitable organic builders and/or chelants are selected from the group consisting of: MEA citrate, citric acid, aminoalkylenepoly(alkylene phosphonates), alkali metal ethane 1-hydroxy disphosphonates, and nitrilotrimethylene, phosphonates, diethylene triamine penta (methylene phosphonic acid) (DTPMP), ethylene diamine tetra(methylene phosphonic acid) (EDT1\41P), hexamethylene diamine tetra(methylene phosphonic acid), hydroxy- ethylene 1,1 diphosphonic acid (REDP), hydroxyethane dimethylene phosphonic acid, ethylene di-amine di-succinic acid (EDDS), ethylene diamine tetraacetic acid (EDTA), hydroxyethylethylenediamine triacetate (HEDTA), nitrilotriacetate (NTA), methylglycinediacetate (MGDA), iminodisuccinate (IDS), hydroxyethyliminodisuccinate (HID S), hydroxyethyliminodiacetate (HEIDA), glycine diacetate (GLDA), diethylene triamine pentaacetic acid (DTPA), catechol sulphonates such as TironTm and mixtures thereof.
Enzymes: Suitable enzymes provide cleaning performance and/or fabric care benefits.
Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenol oxi dases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, B-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and known amylases, or combinations thereof. A preferred enzyme combination comprises a cocktail of conventional detersive enzymes such as protease, lipase, cutinase and/or cellulase in conjunction with amylase. Detersive enzymes are described in greater detail in U.S.
Enzymes: Suitable enzymes provide cleaning performance and/or fabric care benefits.
Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenol oxi dases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, B-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and known amylases, or combinations thereof. A preferred enzyme combination comprises a cocktail of conventional detersive enzymes such as protease, lipase, cutinase and/or cellulase in conjunction with amylase. Detersive enzymes are described in greater detail in U.S.
16 Patent No. 6,579,839.
Enzyme stabiliser: Enzymes can be stabilized using any known stabilizer system such as calcium and/or magnesium compounds, boron compounds and substituted boric acids, aromatic borate esters, peptides and peptide derivatives, polyols, low molecular weight carboxylates, relatively hydrophobic organic compounds [e.g. certain esters, dialcyl glycol ethers, alcohols or alcohol alkoxylates], alkyl ether carboxylate in addition to a calcium ion source, benzamidine hypochlorite, lower aliphatic alcohols and carboxylic acids, N,N-bis(carboxymethyl) serine salts;
(meth)acrylic acid-(meth)acrylic acid ester copolymer and PEG; lignin compound, polyamide oligomer, glycolic acid or its salts; poly hexa methylene bi guanide or N,N-bis-3-amino-propyl-dodecyl amine or salt; and mixtures thereof.
Hueing dyes: The detergent composition may comprise fabric hueing agent (sometimes referred to as shading, bluing, or whitening agents). Typically, the hueing agent provides a blue or violet shade to fabric. Hueing agents can be used either alone or in combination to create a specific shade of hueing and/or to shade different fabric types. This may be provided for example by mixing a red and green-blue dye to yield a blue or violet shade. Hueing agents may be selected from any known chemical class of dye, including but not limited to acridine, anthraquinone (including polycyclic quinones), azine, azo (e.g., monoazo, disazo, trisazo, tetrakisazo, polyazo), including premetallized azo, benzodifurane and benzodifuranone, carotenoid, coumarin, cyanine, diazahemicyanine, diphenylmethane, formazan, hemicyanine, indigoids, methane, naphthalimides, naphthoquinone, nitro and nitroso, oxazine, phthalocyanine, pyrazoles, stilbene, styryl, triarylmethane, triphenylmethane, xanthenes and combinations thereof Optical brighteners: The detergent composition may comprise, based on the total detergent composition weight, from 0.005% to 2.0%, preferably 0.01% to 0.1% of a fluorescent agent (optical brightener). Fluorescent agents are well known and many fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts. Preferred classes of fluorescent agent are: Di -styryl biphenyl compounds, e.g. Tinopal CBS-X, Di-amine stilbene di-sulphonic acid compounds, e.g.
Tinopal DMS pure Xtra and Blankophor HRH, and Pyrazoline compounds, e.g.
Blankophor SN. Preferred fluorescers are: sodium 2-(4-styry1-3-sulphopheny1)-2H-napthol[1 ,2-d]trazole, di sodium 4,4'-bi s{ [(4-anilino-6-(N methyl-N-2 hydroxyethyl) amino 1 , 3 ,5-tri azin -2-yl)]aminoIstilbene-2-2' disulphonate, disodium 4,4'-bis{[(4-anilino-6-morpholino-1 ,3,5-triazin-2-y1)]anninol stilbene-2-2' disulphonate, and di sodium 4,4'-bis(2-sulphoslyryl)biphenyl.
Hydrotrope: The detergent composition may comprise, based on the total detergent
Enzyme stabiliser: Enzymes can be stabilized using any known stabilizer system such as calcium and/or magnesium compounds, boron compounds and substituted boric acids, aromatic borate esters, peptides and peptide derivatives, polyols, low molecular weight carboxylates, relatively hydrophobic organic compounds [e.g. certain esters, dialcyl glycol ethers, alcohols or alcohol alkoxylates], alkyl ether carboxylate in addition to a calcium ion source, benzamidine hypochlorite, lower aliphatic alcohols and carboxylic acids, N,N-bis(carboxymethyl) serine salts;
(meth)acrylic acid-(meth)acrylic acid ester copolymer and PEG; lignin compound, polyamide oligomer, glycolic acid or its salts; poly hexa methylene bi guanide or N,N-bis-3-amino-propyl-dodecyl amine or salt; and mixtures thereof.
Hueing dyes: The detergent composition may comprise fabric hueing agent (sometimes referred to as shading, bluing, or whitening agents). Typically, the hueing agent provides a blue or violet shade to fabric. Hueing agents can be used either alone or in combination to create a specific shade of hueing and/or to shade different fabric types. This may be provided for example by mixing a red and green-blue dye to yield a blue or violet shade. Hueing agents may be selected from any known chemical class of dye, including but not limited to acridine, anthraquinone (including polycyclic quinones), azine, azo (e.g., monoazo, disazo, trisazo, tetrakisazo, polyazo), including premetallized azo, benzodifurane and benzodifuranone, carotenoid, coumarin, cyanine, diazahemicyanine, diphenylmethane, formazan, hemicyanine, indigoids, methane, naphthalimides, naphthoquinone, nitro and nitroso, oxazine, phthalocyanine, pyrazoles, stilbene, styryl, triarylmethane, triphenylmethane, xanthenes and combinations thereof Optical brighteners: The detergent composition may comprise, based on the total detergent composition weight, from 0.005% to 2.0%, preferably 0.01% to 0.1% of a fluorescent agent (optical brightener). Fluorescent agents are well known and many fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts. Preferred classes of fluorescent agent are: Di -styryl biphenyl compounds, e.g. Tinopal CBS-X, Di-amine stilbene di-sulphonic acid compounds, e.g.
Tinopal DMS pure Xtra and Blankophor HRH, and Pyrazoline compounds, e.g.
Blankophor SN. Preferred fluorescers are: sodium 2-(4-styry1-3-sulphopheny1)-2H-napthol[1 ,2-d]trazole, di sodium 4,4'-bi s{ [(4-anilino-6-(N methyl-N-2 hydroxyethyl) amino 1 , 3 ,5-tri azin -2-yl)]aminoIstilbene-2-2' disulphonate, disodium 4,4'-bis{[(4-anilino-6-morpholino-1 ,3,5-triazin-2-y1)]anninol stilbene-2-2' disulphonate, and di sodium 4,4'-bis(2-sulphoslyryl)biphenyl.
Hydrotrope: The detergent composition may comprise, based on the total detergent
17 composition weight, from 0 to 30%, preferably from 0.5 to 5%, more preferably from 1.0 to 3.0%, which can prevent liquid crystal formation. The addition of the hydrotrope thus aids the clarity/transparency of the composition. Suitable hydrotropes comprise but are not limited to urea, salts of benzene sulphonate, toluene sulphonate, xylene sulphonate or cumene sulphonate.
Preferably, the hydrotrope is selected from the group consisting of propylene glycol, xylene sulphonate, ethanol, and urea to provide optimum performance.
Particles: The composition can also comprise particles, especially when the composition further comprises a structurant or thickener. The composition may comprise, based on the total composition weight, from 0.02% to 10%, preferably from 0.1% to 4.0%, more preferably from 0.25% to 2.5% of particles. Said particles include beads, pearlescent agents, capsules, and mixtures thereof.
Suitable capsules are typically formed by at least partially, preferably fully, surrounding a benefit agent with a wall material. Preferably, the capsule is a perfume capsule, wherein said benefit agent comprises one or more perfume raw materials. The capsule wall material may comprise: melamine, polyacrylamide, silicones, silica, polystyrene, polyurea, polyurethanes, polyacrylate based materials, polyacrylate esters based materials, gelatin, styrene malic anhydride, polyamides, aromatic alcohols, polyvinyl alcohol, resorcinol-based materials, poly-isocyanate-based materials, acetals (such as 1,3,5-triol-benzene-gluteraldehyde and 1,3,5-triol-benzene melamine), starch, cellulose acetate phthalate and mixtures thereof.
Preferably, the capsule wall comprises melamine and/or a polyacrylate based material. The perfume capsule may be coated with a deposition aid, a cationic polymer, a non-ionic polymer, an anionic polymer, or mixtures thereof. Preferably, the perfume capsules have a volume weighted mean particle size from 0.1 microns to 100 microns, preferably from 0.5 microns to 60 microns. Especially where the composition comprises capsules having a shell formed at least partially from formaldehyde, the composition can additionally comprise one or more formaldehyde scavengers.
Process of making the laundry detergent composition:
The laundry detergent compositions can be made using any suitable process known to the skilled person. Typically, the ingredients are blended together in any suitable order.
Preferably, the detersive surfactants are added as part of a concentrated premix, to which are added the other optional ingredients. Preferably, the solvent is added either last, or if an external structurant is added, immediately before the external structurant, with the external structurant being added as the last ingredient.
Preferably, the hydrotrope is selected from the group consisting of propylene glycol, xylene sulphonate, ethanol, and urea to provide optimum performance.
Particles: The composition can also comprise particles, especially when the composition further comprises a structurant or thickener. The composition may comprise, based on the total composition weight, from 0.02% to 10%, preferably from 0.1% to 4.0%, more preferably from 0.25% to 2.5% of particles. Said particles include beads, pearlescent agents, capsules, and mixtures thereof.
Suitable capsules are typically formed by at least partially, preferably fully, surrounding a benefit agent with a wall material. Preferably, the capsule is a perfume capsule, wherein said benefit agent comprises one or more perfume raw materials. The capsule wall material may comprise: melamine, polyacrylamide, silicones, silica, polystyrene, polyurea, polyurethanes, polyacrylate based materials, polyacrylate esters based materials, gelatin, styrene malic anhydride, polyamides, aromatic alcohols, polyvinyl alcohol, resorcinol-based materials, poly-isocyanate-based materials, acetals (such as 1,3,5-triol-benzene-gluteraldehyde and 1,3,5-triol-benzene melamine), starch, cellulose acetate phthalate and mixtures thereof.
Preferably, the capsule wall comprises melamine and/or a polyacrylate based material. The perfume capsule may be coated with a deposition aid, a cationic polymer, a non-ionic polymer, an anionic polymer, or mixtures thereof. Preferably, the perfume capsules have a volume weighted mean particle size from 0.1 microns to 100 microns, preferably from 0.5 microns to 60 microns. Especially where the composition comprises capsules having a shell formed at least partially from formaldehyde, the composition can additionally comprise one or more formaldehyde scavengers.
Process of making the laundry detergent composition:
The laundry detergent compositions can be made using any suitable process known to the skilled person. Typically, the ingredients are blended together in any suitable order.
Preferably, the detersive surfactants are added as part of a concentrated premix, to which are added the other optional ingredients. Preferably, the solvent is added either last, or if an external structurant is added, immediately before the external structurant, with the external structurant being added as the last ingredient.
18 Method of laundering fabrics:
The laundry detergent compositions of the present invention can be used to launder fabrics.
In particular, the laundry detergent composition comprising the branched nonionic surfactant can be used for improving the color protection, preferably color retention, of colored fabrics during laundering.
The laundry detergent compositions of the present invention are particularly useful for preventing the removal of fabric-dyes selected from the group consisting of:
reactive dyes, disperse dyes, and mixtures thereof, preferably wherein the fabric dyes are selected from the group consisting of: disperse dyes, reactive dyes, and mixtures thereof, from fabrics during the laundering process.
The compositions of the present invention are particularly effective for reducing the removal of dyes from fabrics comprising cotton, especially cotton-comprising fabrics having dyes selected from the group consisting of: reactive dyes, disperse dyes, direct dyes, vat dyes, and mixtures thereof; preferably wherein the reactive dyes are selected from the group consisting of:
the reactive dyes are selected from the group consisting of: reactive black 5, reactive red 239, reactive red 195, the direct dyes are selected from the group consisting of.
direct black 22, direct red 83, and the vat dyes are selected from the group consisting of: indigo (vat blue 1), sulphur black 1, and mixtures thereof. The compositions of the present invention are particularly useful for reducing the removal of dyes from cotton-comprising fabrics having dyes selected from the group consisting of: reactive dyes, especially reactive dyes selected from the group consisting of:
reactive black 5 , reactive red 239, and mixtures thereof.
The compositions of the present invention are also effective for reducing the removal of dyes from fabrics comprising polyester, especially polyester-comprising fabrics comprising disperse dyes selected from the group consisting of: disperse orange 30, disperse red 167, disperse blue 79, disperse red 60, and mixtures thereof, preferably disperse blue 79.
In such methods and uses, the laundry detergent composition can be diluted to provide a wash liquor having a total surfactant concentration of greater than 300 ppm, preferably from 400 ppm to 2,500 ppm, more preferably from 600 ppm to 1000 ppm. The fabric is then washed in the wash liquor, and preferably rinsed.
METHODS:
A) pH measurement:
The pH is measured, at 25 C, using a Santarius PT-10P pH meter with gel-filled probe (such as
The laundry detergent compositions of the present invention can be used to launder fabrics.
In particular, the laundry detergent composition comprising the branched nonionic surfactant can be used for improving the color protection, preferably color retention, of colored fabrics during laundering.
The laundry detergent compositions of the present invention are particularly useful for preventing the removal of fabric-dyes selected from the group consisting of:
reactive dyes, disperse dyes, and mixtures thereof, preferably wherein the fabric dyes are selected from the group consisting of: disperse dyes, reactive dyes, and mixtures thereof, from fabrics during the laundering process.
The compositions of the present invention are particularly effective for reducing the removal of dyes from fabrics comprising cotton, especially cotton-comprising fabrics having dyes selected from the group consisting of: reactive dyes, disperse dyes, direct dyes, vat dyes, and mixtures thereof; preferably wherein the reactive dyes are selected from the group consisting of:
the reactive dyes are selected from the group consisting of: reactive black 5, reactive red 239, reactive red 195, the direct dyes are selected from the group consisting of.
direct black 22, direct red 83, and the vat dyes are selected from the group consisting of: indigo (vat blue 1), sulphur black 1, and mixtures thereof. The compositions of the present invention are particularly useful for reducing the removal of dyes from cotton-comprising fabrics having dyes selected from the group consisting of: reactive dyes, especially reactive dyes selected from the group consisting of:
reactive black 5 , reactive red 239, and mixtures thereof.
The compositions of the present invention are also effective for reducing the removal of dyes from fabrics comprising polyester, especially polyester-comprising fabrics comprising disperse dyes selected from the group consisting of: disperse orange 30, disperse red 167, disperse blue 79, disperse red 60, and mixtures thereof, preferably disperse blue 79.
In such methods and uses, the laundry detergent composition can be diluted to provide a wash liquor having a total surfactant concentration of greater than 300 ppm, preferably from 400 ppm to 2,500 ppm, more preferably from 600 ppm to 1000 ppm. The fabric is then washed in the wash liquor, and preferably rinsed.
METHODS:
A) pH measurement:
The pH is measured, at 25 C, using a Santarius PT-10P pH meter with gel-filled probe (such as
19 the Toledo probe, part number 52 000 100), calibrated according to the instruction manual. The pH is measured in a 10% dilution in demineralised water (i.e. 1 part laundry detergent composition and 9 parts demineralised water).
B) Method of measuring viscosity:
The viscosity is measured using an AR 2000 rheometer from TA instruments using a cone and plate geometry with a 40 mm diameter and an angle of 1 . The viscosity at the different shear rates is measured via a logarithmic shear rate sweep from 0.1 s-1 to 1200 s-1 in 3 minutes time at
B) Method of measuring viscosity:
The viscosity is measured using an AR 2000 rheometer from TA instruments using a cone and plate geometry with a 40 mm diameter and an angle of 1 . The viscosity at the different shear rates is measured via a logarithmic shear rate sweep from 0.1 s-1 to 1200 s-1 in 3 minutes time at
20 C. Low shear viscosity is measured at a continuous shear rate of 0.05 s-1.
EXAMPLES:
The following methodology was used to evaluate the impact of branched and linear nonionic surfactants on dye-bleeding during laundering.
Glass vials (size 4 ml) were filled with 2 ml of test detergent solutions, as described below, before subsequently inserting into a thermo-shaker (Echotherm Orbital Shaker) set at the temperature of 40 C. The solutions were kept at this temperature for 15 minutes in order for the temperature to equilibrate.
The colored fabric samples as described below were cut into pieces of 150 1 mg (weighted using an analytical balance). These pieces had an area of circa 2.5x2.5 cm (depending on the fabric used). If needed, additional pieces of the same fabric were added to reach the target weight.
Each textiles piece was folded and then inserted into the vials using a disposable glass stick, so that the fabric was fully covered by the solution, before returning the vial to the thermo-shaker.
The vials were continually shaken (using the medium speed setting) at temperature of 40 C for 60 minutes.
The vials were then removed from the therm o-shaker and the fabrics removed from the test detergent solutions. The solutions were kept in the dark for the time required to reach room temperature (25 C).
The dye desorption was quantified as follows:
950 pi of each solution was placed into a semi-micro plastic cuvette and their absorbance spectra recorded using a UV-vis spectrophotometer (Cary UV-Vis Multicell Peltier, supplied by Agilent), measuring absorbance between 300 nm and 900 nm).
To each solution was added 50 1.11 of a 20 wt% aqueous solution of 2-1442,4,4-trimethylpentan-2-yl)phenoxy]ethanol (Triton X-100, supplied by Sigma Aldrich) and the absorbance spectra between 300 nm and 900 nm was remeasured. The Triton X-100 was added as it was observed that, at the test concentrations used, Triton X-100 strongly reduced the scattering of the tested surfactants in the region overlapping the dye absorption spectra.
A calibration curve of each dye used was obtained using the following procedure:
Firstly, the following reference detergent solution was made:
A 350 ppm aqueous solution of equal weight parts of linear C10-C13 alkylbenzene sulphonic acid (HLAS), linear C12-C15 alkyl ethoxy (3.0) sulphate (AE3.0S), and linear C12-C14 E07 (Lorodac L726, supplied by Sasol) in water of hardness 2.67 mmol CaCO3 equivalence (CaCl2 1.93 mmol, MgC120.64mmo1, 15 gpg) was prepared. The pH of the resultant solution was adjusted to 8.0 using ethanolamine.
2.0 ml of the composition was placed in the glass vial with 150 mg of each fabric, and washed using the procedure above, but at a temperature of 92 C for 15 minutes.
After cooling to room temperature in the dark, 9500 of the resultant solutions comprising desorbed dye were combined with 50 pi of a 20 wt% aqueous solution of 24442,4,4-trimethylpentan-2-yl)phenoxy]ethanol (Triton X-100). The absorbance spectra were measured, as described above, and these solutions were arbitrary fixed as 95% dye desorption. The solutions were diluted in the following media: 95% of the above-described reference detergent solution combined with a 5% of Triton X-100 (20wt%) to obtain a calibration curve for each dye used.
The values of absorbance (of the principal peak of the different dye samples) resulting from the desorption experiments were reported as a percentage of the value of same dye desorbed using the reference detergent solution at 92 C in the calibration procedure described above.
The following solutions were evaluated for their impact on dye bleeding for both dyed cotton fabric (cotton fabric dyed using reactive black 5, supplied by CFT
under product code AISE
code 21) and dyed polyester fabric (polyester fabric dyed using disperse blue 79, supplied by CFT
under product code AISE code 31), and the results given below. Apart from Leg A and F (water), the solutions used in the remaining legs comprised 350 ppm of surfactant.
Table 1. % Desorption @ 40 OC (after 1 hour) vs. desorption at 92 C using the reference
EXAMPLES:
The following methodology was used to evaluate the impact of branched and linear nonionic surfactants on dye-bleeding during laundering.
Glass vials (size 4 ml) were filled with 2 ml of test detergent solutions, as described below, before subsequently inserting into a thermo-shaker (Echotherm Orbital Shaker) set at the temperature of 40 C. The solutions were kept at this temperature for 15 minutes in order for the temperature to equilibrate.
The colored fabric samples as described below were cut into pieces of 150 1 mg (weighted using an analytical balance). These pieces had an area of circa 2.5x2.5 cm (depending on the fabric used). If needed, additional pieces of the same fabric were added to reach the target weight.
Each textiles piece was folded and then inserted into the vials using a disposable glass stick, so that the fabric was fully covered by the solution, before returning the vial to the thermo-shaker.
The vials were continually shaken (using the medium speed setting) at temperature of 40 C for 60 minutes.
The vials were then removed from the therm o-shaker and the fabrics removed from the test detergent solutions. The solutions were kept in the dark for the time required to reach room temperature (25 C).
The dye desorption was quantified as follows:
950 pi of each solution was placed into a semi-micro plastic cuvette and their absorbance spectra recorded using a UV-vis spectrophotometer (Cary UV-Vis Multicell Peltier, supplied by Agilent), measuring absorbance between 300 nm and 900 nm).
To each solution was added 50 1.11 of a 20 wt% aqueous solution of 2-1442,4,4-trimethylpentan-2-yl)phenoxy]ethanol (Triton X-100, supplied by Sigma Aldrich) and the absorbance spectra between 300 nm and 900 nm was remeasured. The Triton X-100 was added as it was observed that, at the test concentrations used, Triton X-100 strongly reduced the scattering of the tested surfactants in the region overlapping the dye absorption spectra.
A calibration curve of each dye used was obtained using the following procedure:
Firstly, the following reference detergent solution was made:
A 350 ppm aqueous solution of equal weight parts of linear C10-C13 alkylbenzene sulphonic acid (HLAS), linear C12-C15 alkyl ethoxy (3.0) sulphate (AE3.0S), and linear C12-C14 E07 (Lorodac L726, supplied by Sasol) in water of hardness 2.67 mmol CaCO3 equivalence (CaCl2 1.93 mmol, MgC120.64mmo1, 15 gpg) was prepared. The pH of the resultant solution was adjusted to 8.0 using ethanolamine.
2.0 ml of the composition was placed in the glass vial with 150 mg of each fabric, and washed using the procedure above, but at a temperature of 92 C for 15 minutes.
After cooling to room temperature in the dark, 9500 of the resultant solutions comprising desorbed dye were combined with 50 pi of a 20 wt% aqueous solution of 24442,4,4-trimethylpentan-2-yl)phenoxy]ethanol (Triton X-100). The absorbance spectra were measured, as described above, and these solutions were arbitrary fixed as 95% dye desorption. The solutions were diluted in the following media: 95% of the above-described reference detergent solution combined with a 5% of Triton X-100 (20wt%) to obtain a calibration curve for each dye used.
The values of absorbance (of the principal peak of the different dye samples) resulting from the desorption experiments were reported as a percentage of the value of same dye desorbed using the reference detergent solution at 92 C in the calibration procedure described above.
The following solutions were evaluated for their impact on dye bleeding for both dyed cotton fabric (cotton fabric dyed using reactive black 5, supplied by CFT
under product code AISE
code 21) and dyed polyester fabric (polyester fabric dyed using disperse blue 79, supplied by CFT
under product code AISE code 31), and the results given below. Apart from Leg A and F (water), the solutions used in the remaining legs comprised 350 ppm of surfactant.
Table 1. % Desorption @ 40 OC (after 1 hour) vs. desorption at 92 C using the reference
21 detergent solution for cotton fabrics Leg Test solution % desorption of reactive black 5 dye from cotton A water' 46.8 reference detergent solution2 64.9 linear C12-C14 E073 72.4 2-propy1-1-heptyl E074 51.1 2-propy1-1-heptyl (P0)3(E0)12(P0)155 47.4 1 hardness 2.67 mmol CaCO3 equivalence (15 gpg) 2 I : I : I weight ratio of linear C10-C13 alkylbenzene sulphonic acid (HLAS), linear C12-C15 alkyl ethoxy (3.0) sulphate (AE3.0S), and linear C12-C14 E07 (Lordac L726, supplied by Sasol) 3 Lordac L726, supplied by Sasol 4 Lutensol XP70, supplied by BASF
5 Plurafac SLF180, supplied by BASF
Table 2: % Desorption @ 40 OC (after 1 hour) vs. desorption at 92 C using the reference detergent solution for polyester fabrics Leg Test solution % desorption of disperse blue 79 dye from polyester water' 8.5 reference detergent solution2 50.3 linear C12-C14 E073 65.7 2-propy1-1-heptyl E074 10.3 2-propy1-1-heptyl (P0)3(E0)12(P0)155 12.4 The effect on detergents on dye bleeding from fabric during laundering can be seen from comparing the dye desorption from leg B with leg A for cotton fabrics and leg G with leg F for polyester fabrics.
5 Plurafac SLF180, supplied by BASF
Table 2: % Desorption @ 40 OC (after 1 hour) vs. desorption at 92 C using the reference detergent solution for polyester fabrics Leg Test solution % desorption of disperse blue 79 dye from polyester water' 8.5 reference detergent solution2 50.3 linear C12-C14 E073 65.7 2-propy1-1-heptyl E074 10.3 2-propy1-1-heptyl (P0)3(E0)12(P0)155 12.4 The effect on detergents on dye bleeding from fabric during laundering can be seen from comparing the dye desorption from leg B with leg A for cotton fabrics and leg G with leg F for polyester fabrics.
22 From comparing the dye-bleeding from legs D and E with leg C, it can be seen that branched nonionic surfactants provide reduced dye bleeding than linear branched nonionic surfactants when laundering cottons. A comparison of legs I and J with leg H
demonstrates the same benefit for branched nonionics when laundering polyester fabrics.
From legs B and G, it can be seen that dye bleeding is lower for both cotton ands polyester fabrics when the wash temperature is reduced (from 92 C to 40 C).
The following comparative test demonstrates the reduction in dye bleeding during laundering when using the compositions of the present invention.
The following compositions were prepared by simple mixing.
Table 3: Comparative laundry liquid compositions (examples A and B and inventive laundry liquid composition (example 1) Ex A Ex B
Ex 1 wt% wt%
wt%
C10-C13 linear alkyl benzene sulphonate 3.6 3.6 3.6 C12-C15 AE3.0S 2.5 2.5 2.5 linear C12-C14 E073 2.2 2.2 2-propyl- I -heptyl E074 2.2 C12-C14 dimethyl aminoxide 0.33 0.33 0.33 TPK Fatty Acid 2.16 2.16 2.16 Citric Acid 1.7 1.7 1.7 Polyquaternium 226 1.4 1.4 PEG-PVAc Polymer' 0.5 0.5 0.5 Enzymes 0.006 0.006 0.006 Ethylene diamine tetra(methylene 0.55 0.55 0.55 phosphonic) acid (EDTMP) Perfume 0.82 0.82 0.82 Water to 100% to 100% to 100%
6 cationic polymer Merquat 281, molecular weight 450,000 Da, supplied by Lubrizol 7 Polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains, supplied by BASF, Germany Cotton fabrics pre-dyed with reactive red 239 (AISE 17, supplied by CFT) were cut into 6cm x 6cm pieces. If needed to avoid fraying of the fabric edges, a plastic edging was applied with heat to the fabric squares.
demonstrates the same benefit for branched nonionics when laundering polyester fabrics.
From legs B and G, it can be seen that dye bleeding is lower for both cotton ands polyester fabrics when the wash temperature is reduced (from 92 C to 40 C).
The following comparative test demonstrates the reduction in dye bleeding during laundering when using the compositions of the present invention.
The following compositions were prepared by simple mixing.
Table 3: Comparative laundry liquid compositions (examples A and B and inventive laundry liquid composition (example 1) Ex A Ex B
Ex 1 wt% wt%
wt%
C10-C13 linear alkyl benzene sulphonate 3.6 3.6 3.6 C12-C15 AE3.0S 2.5 2.5 2.5 linear C12-C14 E073 2.2 2.2 2-propyl- I -heptyl E074 2.2 C12-C14 dimethyl aminoxide 0.33 0.33 0.33 TPK Fatty Acid 2.16 2.16 2.16 Citric Acid 1.7 1.7 1.7 Polyquaternium 226 1.4 1.4 PEG-PVAc Polymer' 0.5 0.5 0.5 Enzymes 0.006 0.006 0.006 Ethylene diamine tetra(methylene 0.55 0.55 0.55 phosphonic) acid (EDTMP) Perfume 0.82 0.82 0.82 Water to 100% to 100% to 100%
6 cationic polymer Merquat 281, molecular weight 450,000 Da, supplied by Lubrizol 7 Polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains, supplied by BASF, Germany Cotton fabrics pre-dyed with reactive red 239 (AISE 17, supplied by CFT) were cut into 6cm x 6cm pieces. If needed to avoid fraying of the fabric edges, a plastic edging was applied with heat to the fabric squares.
23 Tergotometer pots were filled with 4.3 grs of each example composition and water (hardness 2.67 mmol CaCO3 equivalence (15 gpg)) added to form 1L of wash liquor. To each tergotometer pot was added the following fabric swatches:
- 3 swatches of reactive red 239 - ballast of 5gr of black cotton - ballast of 3 grs black polyester - other colored 6x6 cm swatches until a total fabric load of 45 g is reached The tergotometer pots were heated to a temperature of 60 C and agitated at a rate of 300 rpm for 40 minutes. After the wash, the test fabrics and ballast were spun at a speed of 1000rpm for 2 minutes before rinsing twice in water at a temperature of 20 C and hardness 2.67 mmol CaCO3 equivalence (15 gpg) for 5 minutes, with a spin step of 1000 rpm for 2 minutes after each rinse step. In a final step, the fabrics were them tumble-dried. The laundering cycles were repeated for a total of 5 cycles.
The test swatches were analysed for colour change versus an unwashed reference fabric using a spectrophotometer (Konika Minolta CM-3610A) and the change in colour measured on the AE CMC scale. The results are given in table 4 below.
Each pot contained three pieces of each of the test fabrics (three internal replicates); each composition was added to two different pots (two external replicates), AE CMC
readings were averaged for each treatment.
Table 4: AE CMC for washed fabric vs. unwashed fabric (lower value corresponds to less fading) Reactive Red 239 Cotton fabric Ex A (comprising linear nonionic surfactant and no 4.6 cationic polymer) Ex B (comprising linear nonionic surfactant and cationic 4.2s*
polymer)
- 3 swatches of reactive red 239 - ballast of 5gr of black cotton - ballast of 3 grs black polyester - other colored 6x6 cm swatches until a total fabric load of 45 g is reached The tergotometer pots were heated to a temperature of 60 C and agitated at a rate of 300 rpm for 40 minutes. After the wash, the test fabrics and ballast were spun at a speed of 1000rpm for 2 minutes before rinsing twice in water at a temperature of 20 C and hardness 2.67 mmol CaCO3 equivalence (15 gpg) for 5 minutes, with a spin step of 1000 rpm for 2 minutes after each rinse step. In a final step, the fabrics were them tumble-dried. The laundering cycles were repeated for a total of 5 cycles.
The test swatches were analysed for colour change versus an unwashed reference fabric using a spectrophotometer (Konika Minolta CM-3610A) and the change in colour measured on the AE CMC scale. The results are given in table 4 below.
Each pot contained three pieces of each of the test fabrics (three internal replicates); each composition was added to two different pots (two external replicates), AE CMC
readings were averaged for each treatment.
Table 4: AE CMC for washed fabric vs. unwashed fabric (lower value corresponds to less fading) Reactive Red 239 Cotton fabric Ex A (comprising linear nonionic surfactant and no 4.6 cationic polymer) Ex B (comprising linear nonionic surfactant and cationic 4.2s*
polymer)
24 Ex 1 (comprising branched nonionic surfactant and cationic 3.9s*
polymer) * significancy calculated vs Ex A via Anova HSD with alpha=0.05 As can be seen from the data above, laundering with the composition of the present invention (example 1) resulted in less dye fading than from comparative compositions which comprised a cationic polymer and linear nonionic surfactant (example B) or no cationic polymer and a nonionic surfactant.
Table 5: further examples of compositions of the present invention.
Ex 2 Ex 3 Ex 4 wt% wt%
wt%
C 1 O-C 13 linear alkyl benzene sulphonate 5 3 3,6 C12-C15 AE3.0S 2.2 3 2.2 linear C12-C14 E073 2-propy1-1-heptyl E074 3 2-propy1-1-heptyl (P0)3(E0)12(P0)155 1.9 2.5 C12-C14 dimethyl aminoxide 0.5 0.1 0.4 TPK Fatty Acid 1 0.5 2 Citric Acid 1 0.5 1.5 Polyquaternium 226 1.5 Polyquaternium 78 1 0.5 PEG-PVAe Polymer' 0.5 0.2 0.3 Enzymes 0.001 0.001 0.001 Ethylene diamine tetra(methylene 0.5 0.4 0.3 phosphonic) acid (EDTMP) Perfume 1.0 0.8 1.2 Water to 100% to 100% to 100%
poly(diallyldimethylammonium chloride / acrylamide), Merquat 740, molecular weight 100,000 Da, supplied by Lubrizol The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as -40 mm" is intended to mean "about 40 mm".
polymer) * significancy calculated vs Ex A via Anova HSD with alpha=0.05 As can be seen from the data above, laundering with the composition of the present invention (example 1) resulted in less dye fading than from comparative compositions which comprised a cationic polymer and linear nonionic surfactant (example B) or no cationic polymer and a nonionic surfactant.
Table 5: further examples of compositions of the present invention.
Ex 2 Ex 3 Ex 4 wt% wt%
wt%
C 1 O-C 13 linear alkyl benzene sulphonate 5 3 3,6 C12-C15 AE3.0S 2.2 3 2.2 linear C12-C14 E073 2-propy1-1-heptyl E074 3 2-propy1-1-heptyl (P0)3(E0)12(P0)155 1.9 2.5 C12-C14 dimethyl aminoxide 0.5 0.1 0.4 TPK Fatty Acid 1 0.5 2 Citric Acid 1 0.5 1.5 Polyquaternium 226 1.5 Polyquaternium 78 1 0.5 PEG-PVAe Polymer' 0.5 0.2 0.3 Enzymes 0.001 0.001 0.001 Ethylene diamine tetra(methylene 0.5 0.4 0.3 phosphonic) acid (EDTMP) Perfume 1.0 0.8 1.2 Water to 100% to 100% to 100%
poly(diallyldimethylammonium chloride / acrylamide), Merquat 740, molecular weight 100,000 Da, supplied by Lubrizol The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as -40 mm" is intended to mean "about 40 mm".
Claims (14)
1. A laundry detergent composition comprising a surfactant system and cationic polymer, wherein the surfactant system comprises: a branched nonionic surfactant, and wherein the cationic polymer is selected from: poly (diallyldimethylammonium chloride);
copolymer of diallyldimethylammonium chloride and acrylic acid; copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride; copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid;
copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid;
copolymer of acryl am i de and N,N, N-trim ethyl am i n oethyl acryl ate; copolym er of diallyldimethylammonium chloride and vinyl alcohol, and mixtures thereof, wherein the cationic polymer has a molecular weight of from 1,000 Da to 1,250,000 Da, wherein the branched nonionic surfactant selected from:
a) Formula I: R1-CII(R2)-0-(P0)x(E0)y(P0)z-II
wherein, in Formula I:
R1 is a C4 to C14 alkyl chain, preferably C4 to CS, more preferably C6;
R2 is a Cl to C7 alkyl chain, preferably a C1 to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
b) Formula II: R1-CH(R2)CH2-0-(P0),(E0)y(P0)z-H
wherein in formula II:
R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
c) and mixtures thereof.
copolymer of diallyldimethylammonium chloride and acrylic acid; copolymer of acrylamide and methacrylamidopropyltrimethyl ammonium chloride; copolymer of acrylamide and diallyldimethylammonium chloride; copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; copolymer of acrylamide, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid;
copolymer of acrylamide, diallyldimethylammonium chloride, and acrylic acid;
copolymer of acryl am i de and N,N, N-trim ethyl am i n oethyl acryl ate; copolym er of diallyldimethylammonium chloride and vinyl alcohol, and mixtures thereof, wherein the cationic polymer has a molecular weight of from 1,000 Da to 1,250,000 Da, wherein the branched nonionic surfactant selected from:
a) Formula I: R1-CII(R2)-0-(P0)x(E0)y(P0)z-II
wherein, in Formula I:
R1 is a C4 to C14 alkyl chain, preferably C4 to CS, more preferably C6;
R2 is a Cl to C7 alkyl chain, preferably a C1 to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
b) Formula II: R1-CH(R2)CH2-0-(P0),(E0)y(P0)z-H
wherein in formula II:
R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
c) and mixtures thereof.
2. The laundry detergent composition according to claim 1, wherein surfactant system comprises the branched nonionic surfactant at a level of from 0.1% to 12%, preferably from 0.5% to 10%, more preferably from 1% to 3% by weight of the composition.
3. The laundry detergent composition according to any preceding claims, wherein the laundry composition comprises the surfactant system at a level of from 1 wt% to 70 wt%, preferably from 10 wt% to 50 wt%, more preferably from 15 wt% to 35 wt%.
4. The laundry detergent composition according to any preceding claim, wherein the surfactant system further comprises an anionic surfactant, preferably selected from the group consisting of: sulphonate surfactant, sulphate surfactant, and mixtures thereof, more preferably wherein the anionic surfactant comprises sulphonate surfactant and sulphate surfactant.
5. The laundry detergent composition according to claim 4, wherein the anionic surfactant comprises alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has an average degree of ethoxylation of from 0.5 to 8.0, preferably from 1.0 to 5.0, more preferably from 2.0 to 3.5.
6. The laundry detergent composition according to claim 4, wherein the anionic surfactant comprises alkyl sulphate surfactant, wherein the alkyl sulphate surfactant has an average degree of ethoxylation of less than 0.5, preferably wherein the alkyl sulphate surfactant comprises branched alkyl sulphate surfactant, more preferably wherein the branched alkyl sulphate surfactant comprises at least 20% by weight of the alkyl chains of the branched alkyl sulphate surfactant of 2-branched alkyl chains.
7. The laundry detergent composition according to any preceding claim, wherein the surfactant system comprises amphoteric and/or zwitterionic surfactant, preferably amphoteric surfactant selected from amine oxide surfactant, more preferably wherein the amine oxide surfactant is lauryl dimethylamine oxide.
8. The laundry detergent composition according to any preceding claim, wherein the cationic polymer is selected from the group consisting of: the cationic polymer is selected from: poly (di allyl di m ethyl amm onium chloride); copolymer of di allyl di m ethyl amm onium chloride and acrylic acid; copolymer of methacrylate, methacrylamidopropyltrimethyl ammonium chloride and acrylic acid; and mixtures thereof, preferably a copolymer of diallyldimethylammonium chloride and acrylic acid.
9. The laundry detergent composition according to any preceding claim, wherein the diallyldimethylammonium chloride and co-acrylic acid monomers are present in a mol ratio of from 50:50 to 90:10, preferably from 55:45 to 85:15, more preferably from 60:40 to 70:30.
10. The laundry detergent composition according to any preceding claim, wherein the cationic polymer has a molecular weight of from 100,000 Da to 1,000,000 Da, more preferably from 250,000 Da to 750,000 Da.
11. The laundry detergent composition according to any preceding claim, wherein the cationic polymer is present at a level of from 0.1% to 10%, preferably 0.5% to 5.0%, more preferably from 1.0 to 2.5% by weight of the composition.
12. The use of a laundry detergent composition comprising a branched nonionic surfactant for improving the colour protection, preferably colour retention, of coloured fabrics during laundering.
13. The use according to claim 12, wherein the branched nonionic surfactant selected from.
a) Formula I: R1-CH(R2)-0-(P0)),(E0)y(P0)7-H
wherein, in Formula I:
R1 is a C4 to C14 alkyl chain, preferably C4 to C8, more preferably C6;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
b) Formula II: R1-CH(R2)CH2-0-(PO)(EO)y(P0)z-H
R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation.
a) Formula I: R1-CH(R2)-0-(P0)),(E0)y(P0)7-H
wherein, in Formula I:
R1 is a C4 to C14 alkyl chain, preferably C4 to C8, more preferably C6;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation;
b) Formula II: R1-CH(R2)CH2-0-(PO)(EO)y(P0)z-H
R1 is a C3 to C13 alkyl chain, preferably C3 to C7, more preferably C5;
R2 is a C1 to C7 alkyl chain, preferably a Cl to C5, more preferably C3 alkyl chain;
x is from 0 to 10, preferably from 0 to 5, more preferably from 0 to 3;
y is from 5 to 20, preferably from 6 to 15, more preferably from 7 to 12;
z is from 0 to 20, preferably from 0 to 5, more preferably from 0 to 3;
EO stands for ethoxylation and PO stands for propoxylation.
14.
The use according to any of claims 12 to 13, wherein the fabric-dye is selected from the group consisting of: reactive dyes, disperse dyes, and mixtures thereof, preferably wherein the fabric dyes are selected from the group consisting of: disperse dyes, reactive dyes, and mixtures thereof.
The use according to any of claims 12 to 13, wherein the fabric-dye is selected from the group consisting of: reactive dyes, disperse dyes, and mixtures thereof, preferably wherein the fabric dyes are selected from the group consisting of: disperse dyes, reactive dyes, and mixtures thereof.
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EP22165838.8 | 2022-03-31 | ||
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DE2437090A1 (en) | 1974-08-01 | 1976-02-19 | Hoechst Ag | CLEANING SUPPLIES |
DE3026090A1 (en) * | 1980-07-10 | 1982-02-18 | Henkel KGaA, 4000 Düsseldorf | LIQUID DETERGENT WITH A CONTENT OF DISABLING-INHIBITING |
US4565647B1 (en) | 1982-04-26 | 1994-04-05 | Procter & Gamble | Foaming surfactant compositions |
US5104646A (en) | 1989-08-07 | 1992-04-14 | The Procter & Gamble Company | Vehicle systems for use in cosmetic compositions |
US5106609A (en) | 1990-05-01 | 1992-04-21 | The Procter & Gamble Company | Vehicle systems for use in cosmetic compositions |
CA2396974C (en) | 2000-02-23 | 2006-06-27 | The Procter & Gamble Company | Liquid laundry detergent compositions having enhanced clay removal benefits |
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PL2225355T3 (en) | 2007-11-09 | 2017-01-31 | Procter & Gamble | Cleaning compositions comprising a multi-polymer system comprising at least one alkoxylated grease cleaning polymer |
JP5871468B2 (en) | 2008-02-15 | 2016-03-01 | ザ プロクター アンド ギャンブルカンパニー | Liquid detergent composition comprising an external structured system containing a bacterial cellulose network |
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BR112014010907A2 (en) | 2011-11-11 | 2017-05-16 | Procter & Gamble | surface treatment compositions including protective salts |
WO2014139577A1 (en) | 2013-03-14 | 2014-09-18 | Ecolab Usa Inc. | Laundry detergent composition for low temperature washing |
US9840682B2 (en) * | 2014-11-11 | 2017-12-12 | The Procter & Gamble Company | Cleaning compositions with improved sudsing profile comprising a cationic polymer and silicone mixture |
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