CA2126382C - Stable pourable aqueous liquid laundry detergent compositions with peroxyacid bleach - Google Patents
Stable pourable aqueous liquid laundry detergent compositions with peroxyacid bleachInfo
- Publication number
- CA2126382C CA2126382C CA 2126382 CA2126382A CA2126382C CA 2126382 C CA2126382 C CA 2126382C CA 2126382 CA2126382 CA 2126382 CA 2126382 A CA2126382 A CA 2126382A CA 2126382 C CA2126382 C CA 2126382C
- Authority
- CA
- Canada
- Prior art keywords
- aqueous liquid
- stable
- laundry detergent
- composition
- liquid laundry
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 135
- 239000003599 detergent Substances 0.000 title claims abstract description 59
- 239000007788 liquid Substances 0.000 title claims abstract description 39
- 150000004965 peroxy acids Chemical class 0.000 title description 18
- 239000007844 bleaching agent Substances 0.000 title description 6
- -1 xanthan polysaccharide Chemical class 0.000 claims abstract description 54
- 229920001285 xanthan gum Polymers 0.000 claims abstract description 26
- 239000004094 surface-active agent Substances 0.000 claims abstract description 24
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 19
- 239000005017 polysaccharide Substances 0.000 claims abstract description 19
- 239000007787 solid Substances 0.000 claims abstract description 15
- 150000004967 organic peroxy acids Chemical class 0.000 claims abstract description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 13
- 239000000194 fatty acid Substances 0.000 claims abstract description 13
- 229930195729 fatty acid Natural products 0.000 claims abstract description 13
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 13
- 229920001817 Agar Polymers 0.000 claims abstract description 12
- 239000008272 agar Substances 0.000 claims abstract description 12
- 238000004140 cleaning Methods 0.000 claims abstract description 9
- 238000004061 bleaching Methods 0.000 claims abstract description 8
- 229920005862 polyol Polymers 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 150000003077 polyols Chemical class 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 15
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000002736 nonionic surfactant Substances 0.000 claims description 14
- 239000003945 anionic surfactant Substances 0.000 claims description 13
- 238000010790 dilution Methods 0.000 claims description 12
- 239000012895 dilution Substances 0.000 claims description 12
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 10
- 239000000600 sorbitol Substances 0.000 claims description 10
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 9
- 229910021538 borax Inorganic materials 0.000 claims description 9
- 239000004328 sodium tetraborate Substances 0.000 claims description 9
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 9
- KCAZSAYYICOMMG-UHFFFAOYSA-N 6-hydroperoxy-6-oxohexanoic acid Chemical compound OOC(=O)CCCCC(O)=O KCAZSAYYICOMMG-UHFFFAOYSA-N 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 230000002708 enhancing effect Effects 0.000 claims description 7
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- 239000004744 fabric Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 6
- XOHQAXXZXMHLPT-UHFFFAOYSA-N ethyl(phosphonooxy)phosphinic acid Chemical compound CCP(O)(=O)OP(O)(O)=O XOHQAXXZXMHLPT-UHFFFAOYSA-N 0.000 claims description 5
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 claims description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 4
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 4
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 claims description 4
- 108090000790 Enzymes Proteins 0.000 claims description 3
- 102000004190 Enzymes Human genes 0.000 claims description 3
- 239000005715 Fructose Substances 0.000 claims description 3
- 229930091371 Fructose Natural products 0.000 claims description 3
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 3
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- 150000001639 boron compounds Chemical class 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 239000000811 xylitol Substances 0.000 claims description 3
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 3
- 235000010447 xylitol Nutrition 0.000 claims description 3
- 229960002675 xylitol Drugs 0.000 claims description 3
- KOEDSBONUVRKAF-UHFFFAOYSA-N 4-(nonylamino)-4-oxobutaneperoxoic acid Chemical compound CCCCCCCCCNC(=O)CCC(=O)OO KOEDSBONUVRKAF-UHFFFAOYSA-N 0.000 claims description 2
- AVLQNPBLHZMWFC-UHFFFAOYSA-N 6-(nonylamino)-6-oxohexaneperoxoic acid Chemical compound CCCCCCCCCNC(=O)CCCCC(=O)OO AVLQNPBLHZMWFC-UHFFFAOYSA-N 0.000 claims description 2
- 229910011255 B2O3 Inorganic materials 0.000 claims description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- 125000000129 anionic group Chemical group 0.000 claims 4
- 239000008367 deionised water Substances 0.000 claims 2
- 229910021641 deionized water Inorganic materials 0.000 claims 2
- CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 claims 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 239000000047 product Substances 0.000 description 21
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 14
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 239000000230 xanthan gum Substances 0.000 description 11
- 235000010493 xanthan gum Nutrition 0.000 description 11
- 229940082509 xanthan gum Drugs 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
- 239000005639 Lauric acid Substances 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
- WRUGWIBCXHJTDG-UHFFFAOYSA-L magnesium sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Mg+2].[O-]S([O-])(=O)=O WRUGWIBCXHJTDG-UHFFFAOYSA-L 0.000 description 7
- 229940061634 magnesium sulfate heptahydrate Drugs 0.000 description 7
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 7
- QJRVOJKLQNSNDB-UHFFFAOYSA-N 4-dodecan-3-ylbenzenesulfonic acid Chemical compound CCCCCCCCCC(CC)C1=CC=C(S(O)(=O)=O)C=C1 QJRVOJKLQNSNDB-UHFFFAOYSA-N 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- 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 5
- 150000004676 glycans Chemical class 0.000 description 5
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 101000581940 Homo sapiens Napsin-A Proteins 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- 102100027343 Napsin-A Human genes 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003792 electrolyte Substances 0.000 description 3
- 239000006081 fluorescent whitening agent Substances 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 150000002431 hydrogen Chemical group 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 3
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 3
- 235000021286 stilbenes Nutrition 0.000 description 3
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 3
- LMYSNFBROWBKMB-UHFFFAOYSA-N 4-[2-(dipropylamino)ethyl]benzene-1,2-diol Chemical compound CCCN(CCC)CCC1=CC=C(O)C(O)=C1 LMYSNFBROWBKMB-UHFFFAOYSA-N 0.000 description 2
- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-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
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001408 amides Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 235000019820 disodium diphosphate Nutrition 0.000 description 2
- GYQBBRRVRKFJRG-UHFFFAOYSA-L disodium pyrophosphate Chemical compound [Na+].[Na+].OP([O-])(=O)OP(O)([O-])=O GYQBBRRVRKFJRG-UHFFFAOYSA-L 0.000 description 2
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-K pentetate(3-) Chemical compound OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O QPCDCPDFJACHGM-UHFFFAOYSA-K 0.000 description 2
- 125000000914 phenoxymethylpenicillanyl group Chemical group CC1(S[C@H]2N([C@H]1C(=O)*)C([C@H]2NC(COC2=CC=CC=C2)=O)=O)C 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- WDKWVKZMTODAHS-UHFFFAOYSA-N 2-aminohexaneperoxoic acid Chemical compound CCCCC(N)C(=O)OO WDKWVKZMTODAHS-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 description 1
- JQSMFSPOCAZNQP-UHFFFAOYSA-N 6-(nonylamino)-6-oxohexanoic acid Chemical group CCCCCCCCCNC(=O)CCCCC(O)=O JQSMFSPOCAZNQP-UHFFFAOYSA-N 0.000 description 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical group OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 101710194948 Protein phosphatase PhpP Proteins 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000589634 Xanthomonas Species 0.000 description 1
- ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- ADKBGLXGTKOWIU-UHFFFAOYSA-N butanediperoxoic acid Chemical compound OOC(=O)CCC(=O)OO ADKBGLXGTKOWIU-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001720 carbohydrates Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical class [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- PMPJQLCPEQFEJW-GNTLFSRWSA-L disodium;2-[(z)-2-[4-[4-[(z)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1\C=C/C1=CC=C(C=2C=CC(\C=C/C=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-GNTLFSRWSA-L 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000004688 heptahydrates Chemical group 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 125000000612 phthaloyl group Chemical group C(C=1C(C(=O)*)=CC=CC1)(=O)* 0.000 description 1
- 229940081066 picolinic acid Drugs 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- GHKGUEZUGFJUEJ-UHFFFAOYSA-M potassium;4-methylbenzenesulfonate Chemical compound [K+].CC1=CC=C(S([O-])(=O)=O)C=C1 GHKGUEZUGFJUEJ-UHFFFAOYSA-M 0.000 description 1
- JKLNROLANBRABU-UHFFFAOYSA-N pyridine-2-carboxylic acid;pyridine-2,6-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC=N1.OC(=O)C1=CC=CC=N1.OC(=O)C1=CC=CC(C(O)=O)=N1 JKLNROLANBRABU-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0047—Other compounding ingredients characterised by their effect pH regulated 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/046—Salts
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2034—Monohydric alcohols aromatic
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/221—Mono, di- or trisaccharides or derivatives thereof
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
-
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Molecular Biology (AREA)
- Detergent Compositions (AREA)
Abstract
Stable, pourable aqueous liquid laundry detergents containing solid, substantially water-insoluble organic peroxyacid, detergent surfactant, agar or xanthan polysaccharide, and a pH jump system are described. A second type of composition also comprises fatty acid and specified amounts and ratios of C8-20 alkyl polyethoxylate for good cleaning and bleaching.
Description
.._ STABLE, POURABLE AQUEOUS LIQUID LAUNDRY DETERGENT
COMPOSITIONS WITH PEROXYACID BLEACH
TECHNICAL FIELD
This relates to stable, pourable aqueous liquid laundry detergents containing solid, substantially water-insoluble organic peroxyacid, detergent surfactant, agar or xanthan polysaccharide, and a pH jump system.
BACKGROUND OF THE INVENTION
U. S. Patents 4,992,194 and 5,073,285, both Liberati et al, issued February 12, 1991 and December 17,1991, respectively, describe aqueous structured heavy duty liquid detergent formulations which contain solid, particulate, substantially water-insoluble organic peroxyacid, surfactant combinations, pH
adjusting systems, and selected decoupling polymers.
U. S. Patent 4,879,057, Dankowski et al, issued November 7, 1989 discloses aqueous bleaching suspensions including peroxycarboxylic acid suspended in a carrier liquid in the presence of an organic thickening agent and of an acidifying agent. The suspensions contain agar or xanthan polysaccharide as thickening agent, and a hydrate-forming neutral salt.
Aqueous liquid laundry detergent products which contain suspended solids such as solid, substantially water-insoluble peroxyacid can have phase stability problems, particularly across the varying environmental temperatures to which such products may be exposed-A further problem is product and wash pH, since low product pH is required for bleach stability while alkaline wash pH is advantageous for cleaning and bleaching efficacy (see U.S. Patent 4,259,201, Cockrell).
Lastly, when product detergent surfactant levels are increased in such compositions for better cleaning and bleaching - 2 - 2 ~ 2 ~ 3 8 ~
. ._ performance, product viscosity often increases to unacceptable levels.
It has now been found that a stable, pourable aqueous liquid laundry detergent composition can be formulated by including from about 0.05 to about 2 weight % of xanthan polysaccharide for phase stability, along with a specific pH jump system for cleaning performance and product bleach stability, in a peroxyacid-containing suspension. This is accomplished without the use of a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
It has also been found that for improved cleaning performance without adversely affecting product viscosity, ethoxylated nonionic surfactant can be added (to the above composition containing peroxyacid and xanthan polysaccharide) in an amount greater than or equal to the amount of anionic surfactant t-o achieve a stable, pourable aqueous liquid detergent composition which cleans and bleaches quite well (even in the absence of enzymes and an effective amount of detergency builder). In this second type of high nonionic composition with product stability and good detergency, certain low levels of fatty acid are also included for phase stability.
SUMMARY OF THE INVENTION
This relates to a stable, pourable aqueous liquid laundry detergent composition, comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
b. fro~ about 5 to about 50% of detergent surfactant;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10;
d. from about 0.05 to about 2% of agar or xanthan polysaccharide; and which laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
2 ~ ~6382 DESCRIPTION OF THE INVENTION
The compositions according to the present invention are aqueous and preferably comprise, by weight of the composition, from about 30 to about 70%, preferably from about 40 to about 60%, of water, preferably distilled and deionized, and from about 30 to about 70%, preferably from about 40 to about 60%, of active ingredients.
A. PeroxYacid Compositions of the present invention comprise from about 0.5 to about 30%, preferably from about 1 to about 20%, most preferably from about 1.5 to about 5%, by weight of the composition, of solid, substantially water-insoluble organic peroxyacid.
The organic peroxyacid should be evenly suspended throughout the liquid detergent composition.
The following organic peroxyacids (IUPAC names) are preferred:
15 4-nonylamino-4-oxoperoxybutyric acid ("NAPSA"); 6-nonylamino-6-oxoperoxyhexanoic acid ("NAPM "); 1,12-diperoxy-dodecanedioic acid, ("DPDA"); heptyl sulfonylperpropionic acid; decylsulphonyl perpropionic acid; heptyl-, octyl-, nonyl-, and decyl-sulphonylperbutyric acid; and phthaloyl aminoperoxycaproic acid.
Of the organic peroxyacids, amidoperoxyacids (amide substituted peroxycarboxylic acids) are preferred. Suitable amidoperoxyacids for use herein are described in U.S. Patents 4,634,551 and 4,686,063, both Burns et al, issued January 6, 1987 and August 11, 1987, respectively.
Suitable amidoperoxyacids are of the formula:
R1 - NH - C - R2 C - OOH or Rl - C - NH - R2 C - OOH
wherein Rl is an alkyl group containing from about 6 to about 12 carbon atoms, and R2 is an alkylene containing from 1 to about 6 carbon atoms.
Preferably, R1 is an alkyl group containing from about 8 to about 10 carbon atoms, and R2 is an alkylene group containing from about 2 to about 4.
L~, Also preferred are peroxyfumarates, which are described in U.S.
Patent 4,852,989, Burns et al, issued August 1, 1989, and sulfone peroxyacids (sulfone peroxycarboxylic acids), which are described in U.S. Patents 4,758,369, 4,824,591, and 5,004,558, all Dryoff et al, issued July 19, 1988, April 25, 1989, and April 2, 1991, respectively.
The most preferred amidoperoxyacids are monononylamido peroxyadipic acid (NAPM; most preferred), monononylamido peroxysuccinic acid (NAPSA), and 1,12-diperoxy-dodecandioic acid (DPDA).
Another name for NAPM is 6-(nonylamino)-6-oxo-caproic acid. The 0 chemical formula for NAPM is:
H O O
CH3(CH2)81l e(CHz)4eOOH
The molecular weight of NAPM is 287.4.
Example I of U.S. Patent 4,686,063 contains one description of the synthesis of NAPSA, from Column 8, line 40 to Column 9, line 5, and NAPM, from Column 9, line 15 to Column 9, line 65. At the end of the amidoperoxyacid synthesis, the reaction is quenched with water, filtered, washed with water to remove some excess sulfuric acid (or 20 other strong acid with which the peroxyacid was made), and filtered again.
The amidoperoxyacid wet cake thus obtained can be contacted with a phosphate buffer solution at a pH between about 3,5 and 6, preferably between about 4 and 5, according to U.S. Patent 4,909,953, Sadlowski et al, issued March 20, 1990. U.S. Patent 5,055,218, Getty et al, issued October 8, 1991, describes bleach granules containing amidoperoxyacid.
NAPM filter cake herein is preferably washed twice in phosphate buffer. It has been found that two successive phosphate buffer washes lend optimal stability to NAPM .
NAPM can be prepared by, for example, first reacting NMM
(mononoyl amide of adipic acid), sulfuric acid, and hydrogen ~;-, -peroxide. The reaction product is quenched by addition to ice water followed by filtration, washing with distilled water, and final suction filtration to recover the wet cake. Washing can be continued until the pH of the filtrate is neutral.
Preferred NAPM is thermally annealed (or thermally agglomerated), meaning that it has been heated up to 70~C and then quenched and filtered.
Also suitable for use herein are phthaloyl aminoperoxycaproic acids ("PAP"), which are described in U.S. Patent 5,073,285, Liberati et al, issued December 17, 1991.
Particulate (solid), organic peroxyacids with a theoretical AvO
(available oxygen) of between about 3 and about 15, most preferably between 5 and 12, are preferred.
B. Deterqent Surfactant The present composition comprises, by weight of the composition, from about 5 to about 50%, preferably from about 10 to about 40%, most preferably from about 15 to about 30%, of detergent surfactant, preferably nonionic and/or anionic surfactant.
Preferred compositions for the second, high nonionic surfactant type of composition with phase stability comprise from about 10 to about 40%, preferably from about 12 to about 30%, most preferably from about 15 to about 20%, by weight of the composition of C8 C20 alcohol which has been ethoxylated with an average of from about 2 to about 20 moles of ethylene oxide per mole of alcohol; and from 0 to about 10%, preferably from about 5 to about 8%, of bleach-compatible anionic surfactant.
More preferred is ClO-Cl8 alcohol which has been ethoxylated with an average of from about 4 to about 15, more preferably from about 6 to about 12, moles of ethylene oxide per mole of alcohol. Blends of C10-Cl8 alkyl ethoxylates and C10-Cl8 alkyl ethoxylates with additional detergent 3 0 surfactants, are also included herein. Most preferred is Clz-Cl5 alkylethoxylate (E6-9), which is C12-C15 alcohol which has been ethoxylated with an average of 6-9 moles of ethylene oxide per mole of alcohol. The most preferred anionic surfactant is C12 linear alkylbenzene sulfonic acid.
w- - 6 - 2 ~ 2 ~ 3 8 2 Preferably, the present compositions comprise ethoxylated nonionic surfactant:anionic surfactant in a ratio of between about 1:1 and about 30:1, preferably between about 2:1 and about 20:1, most preferably between about 2:1 and about 4:1.
These are preferably selected from the group consisting of c9-2o linear alkylbenzene sulfonate, C8-l8 alkenyl carboxysulfonate, E2 20 ethoxylated C10-2o alcohols, polyhydroxy fatty acid amide, and mixtures thereof. More preferred are C10 14 linear alkylbenzene sulfonate (most preferred), and E2 5 0 ethoxylated C12 18 alcohols.
1. Anionic Surfactant Anionic surfactants useful for detersive purposes are included in the compositions hereof. These can include salts of soap, Cg-C20 linear alkylbenzenesulphonates, Cg-C22 primary or secondary alkanesulphonates, Cg-C24 olefinsulphonates, sulphonated polycarboxylic acids prepared by sulphonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British Patent Specification No. 1,082,179, alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, paraffin sulfonates, alkyl phosphates, isothionates such as the acyl isothionates, N-acyl taurates, fatty acid amides of methyl tauride, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C12-C1g monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C6-C14 diesters), N-acyl sarcosinates (the nonionic nonsulfated compounds being described below), branched primary alkyl sulfates, alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH20)kCH2C00-M+ wherein R is a Cg-C22 alkyl, k is an integer from 0 to 10, and M is a soluble salt-forming cation, and fatty acids esterified with isothionic acid and neutralized with sodium hydroxide. Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil.
Further examples are given in ~Surface Active Agents and Detergents~ (Vol. I and II by Schwartz, Perry and Berch). A
variety of such surfactants are also generally disclosed in U.S.
Patent 3,929,678, issued December 30, 1975 to Laughlin, et al. at Column 23, line 58 through Column 29, line 23.
One type of anionic surfactant preferred for use in liquid detergent compositions herein is alkyl ester sulfonates, which is preferably alkyl ester sulfonate surfactant of the structural formula:
R3---cH-- e --oR4 wherein R3 is a C8-C20 hydrocarbyl, preferably an alkyl, or combination thereof, R4 is a Cl-C6 hydrocarbyl, preferably an alkyl, or combination thereof, and M is a soluble salt-forming cation. Suitable salts include metal salts such as sodium, potassium, and lithium salts. Preferably, R3 is C10-Cl6 alkyl, and R4 is methyl, ethyl or isopropyl. Especially preferred are the methyl ester sulfonates wherein R3 is Cl4-Cl6 alkyl.
Preferred for use in liquid detergent compositions herein is Cg-C20 linear alkylbenzene sulfonate (preferably sodium salts).
Preferably the nonionic surfactant is the condensation product of Cl0-C20 alcohol and between about 2 and about 20 moles of ethylene oxide per mole of alcohol ("E220 ethoxylated C10-C20 alcohol").
2. Nonionic Surfactant Suitable nonionic detergent surfactants are generally disclosed in U.S. Patent 3,929,678, Laughlin et al., issued December 30, 1975, at Column 13, line 14 through Column 16, line 6. Exemplary, non-limiting classes of useful nonionic surfactants are listed below.
1. The polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols.
2. The condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide. The alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
,~AY~
~- - 8 - 2 1 2 6 3 ~ 2 3. The condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol.
COMPOSITIONS WITH PEROXYACID BLEACH
TECHNICAL FIELD
This relates to stable, pourable aqueous liquid laundry detergents containing solid, substantially water-insoluble organic peroxyacid, detergent surfactant, agar or xanthan polysaccharide, and a pH jump system.
BACKGROUND OF THE INVENTION
U. S. Patents 4,992,194 and 5,073,285, both Liberati et al, issued February 12, 1991 and December 17,1991, respectively, describe aqueous structured heavy duty liquid detergent formulations which contain solid, particulate, substantially water-insoluble organic peroxyacid, surfactant combinations, pH
adjusting systems, and selected decoupling polymers.
U. S. Patent 4,879,057, Dankowski et al, issued November 7, 1989 discloses aqueous bleaching suspensions including peroxycarboxylic acid suspended in a carrier liquid in the presence of an organic thickening agent and of an acidifying agent. The suspensions contain agar or xanthan polysaccharide as thickening agent, and a hydrate-forming neutral salt.
Aqueous liquid laundry detergent products which contain suspended solids such as solid, substantially water-insoluble peroxyacid can have phase stability problems, particularly across the varying environmental temperatures to which such products may be exposed-A further problem is product and wash pH, since low product pH is required for bleach stability while alkaline wash pH is advantageous for cleaning and bleaching efficacy (see U.S. Patent 4,259,201, Cockrell).
Lastly, when product detergent surfactant levels are increased in such compositions for better cleaning and bleaching - 2 - 2 ~ 2 ~ 3 8 ~
. ._ performance, product viscosity often increases to unacceptable levels.
It has now been found that a stable, pourable aqueous liquid laundry detergent composition can be formulated by including from about 0.05 to about 2 weight % of xanthan polysaccharide for phase stability, along with a specific pH jump system for cleaning performance and product bleach stability, in a peroxyacid-containing suspension. This is accomplished without the use of a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
It has also been found that for improved cleaning performance without adversely affecting product viscosity, ethoxylated nonionic surfactant can be added (to the above composition containing peroxyacid and xanthan polysaccharide) in an amount greater than or equal to the amount of anionic surfactant t-o achieve a stable, pourable aqueous liquid detergent composition which cleans and bleaches quite well (even in the absence of enzymes and an effective amount of detergency builder). In this second type of high nonionic composition with product stability and good detergency, certain low levels of fatty acid are also included for phase stability.
SUMMARY OF THE INVENTION
This relates to a stable, pourable aqueous liquid laundry detergent composition, comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
b. fro~ about 5 to about 50% of detergent surfactant;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10;
d. from about 0.05 to about 2% of agar or xanthan polysaccharide; and which laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
2 ~ ~6382 DESCRIPTION OF THE INVENTION
The compositions according to the present invention are aqueous and preferably comprise, by weight of the composition, from about 30 to about 70%, preferably from about 40 to about 60%, of water, preferably distilled and deionized, and from about 30 to about 70%, preferably from about 40 to about 60%, of active ingredients.
A. PeroxYacid Compositions of the present invention comprise from about 0.5 to about 30%, preferably from about 1 to about 20%, most preferably from about 1.5 to about 5%, by weight of the composition, of solid, substantially water-insoluble organic peroxyacid.
The organic peroxyacid should be evenly suspended throughout the liquid detergent composition.
The following organic peroxyacids (IUPAC names) are preferred:
15 4-nonylamino-4-oxoperoxybutyric acid ("NAPSA"); 6-nonylamino-6-oxoperoxyhexanoic acid ("NAPM "); 1,12-diperoxy-dodecanedioic acid, ("DPDA"); heptyl sulfonylperpropionic acid; decylsulphonyl perpropionic acid; heptyl-, octyl-, nonyl-, and decyl-sulphonylperbutyric acid; and phthaloyl aminoperoxycaproic acid.
Of the organic peroxyacids, amidoperoxyacids (amide substituted peroxycarboxylic acids) are preferred. Suitable amidoperoxyacids for use herein are described in U.S. Patents 4,634,551 and 4,686,063, both Burns et al, issued January 6, 1987 and August 11, 1987, respectively.
Suitable amidoperoxyacids are of the formula:
R1 - NH - C - R2 C - OOH or Rl - C - NH - R2 C - OOH
wherein Rl is an alkyl group containing from about 6 to about 12 carbon atoms, and R2 is an alkylene containing from 1 to about 6 carbon atoms.
Preferably, R1 is an alkyl group containing from about 8 to about 10 carbon atoms, and R2 is an alkylene group containing from about 2 to about 4.
L~, Also preferred are peroxyfumarates, which are described in U.S.
Patent 4,852,989, Burns et al, issued August 1, 1989, and sulfone peroxyacids (sulfone peroxycarboxylic acids), which are described in U.S. Patents 4,758,369, 4,824,591, and 5,004,558, all Dryoff et al, issued July 19, 1988, April 25, 1989, and April 2, 1991, respectively.
The most preferred amidoperoxyacids are monononylamido peroxyadipic acid (NAPM; most preferred), monononylamido peroxysuccinic acid (NAPSA), and 1,12-diperoxy-dodecandioic acid (DPDA).
Another name for NAPM is 6-(nonylamino)-6-oxo-caproic acid. The 0 chemical formula for NAPM is:
H O O
CH3(CH2)81l e(CHz)4eOOH
The molecular weight of NAPM is 287.4.
Example I of U.S. Patent 4,686,063 contains one description of the synthesis of NAPSA, from Column 8, line 40 to Column 9, line 5, and NAPM, from Column 9, line 15 to Column 9, line 65. At the end of the amidoperoxyacid synthesis, the reaction is quenched with water, filtered, washed with water to remove some excess sulfuric acid (or 20 other strong acid with which the peroxyacid was made), and filtered again.
The amidoperoxyacid wet cake thus obtained can be contacted with a phosphate buffer solution at a pH between about 3,5 and 6, preferably between about 4 and 5, according to U.S. Patent 4,909,953, Sadlowski et al, issued March 20, 1990. U.S. Patent 5,055,218, Getty et al, issued October 8, 1991, describes bleach granules containing amidoperoxyacid.
NAPM filter cake herein is preferably washed twice in phosphate buffer. It has been found that two successive phosphate buffer washes lend optimal stability to NAPM .
NAPM can be prepared by, for example, first reacting NMM
(mononoyl amide of adipic acid), sulfuric acid, and hydrogen ~;-, -peroxide. The reaction product is quenched by addition to ice water followed by filtration, washing with distilled water, and final suction filtration to recover the wet cake. Washing can be continued until the pH of the filtrate is neutral.
Preferred NAPM is thermally annealed (or thermally agglomerated), meaning that it has been heated up to 70~C and then quenched and filtered.
Also suitable for use herein are phthaloyl aminoperoxycaproic acids ("PAP"), which are described in U.S. Patent 5,073,285, Liberati et al, issued December 17, 1991.
Particulate (solid), organic peroxyacids with a theoretical AvO
(available oxygen) of between about 3 and about 15, most preferably between 5 and 12, are preferred.
B. Deterqent Surfactant The present composition comprises, by weight of the composition, from about 5 to about 50%, preferably from about 10 to about 40%, most preferably from about 15 to about 30%, of detergent surfactant, preferably nonionic and/or anionic surfactant.
Preferred compositions for the second, high nonionic surfactant type of composition with phase stability comprise from about 10 to about 40%, preferably from about 12 to about 30%, most preferably from about 15 to about 20%, by weight of the composition of C8 C20 alcohol which has been ethoxylated with an average of from about 2 to about 20 moles of ethylene oxide per mole of alcohol; and from 0 to about 10%, preferably from about 5 to about 8%, of bleach-compatible anionic surfactant.
More preferred is ClO-Cl8 alcohol which has been ethoxylated with an average of from about 4 to about 15, more preferably from about 6 to about 12, moles of ethylene oxide per mole of alcohol. Blends of C10-Cl8 alkyl ethoxylates and C10-Cl8 alkyl ethoxylates with additional detergent 3 0 surfactants, are also included herein. Most preferred is Clz-Cl5 alkylethoxylate (E6-9), which is C12-C15 alcohol which has been ethoxylated with an average of 6-9 moles of ethylene oxide per mole of alcohol. The most preferred anionic surfactant is C12 linear alkylbenzene sulfonic acid.
w- - 6 - 2 ~ 2 ~ 3 8 2 Preferably, the present compositions comprise ethoxylated nonionic surfactant:anionic surfactant in a ratio of between about 1:1 and about 30:1, preferably between about 2:1 and about 20:1, most preferably between about 2:1 and about 4:1.
These are preferably selected from the group consisting of c9-2o linear alkylbenzene sulfonate, C8-l8 alkenyl carboxysulfonate, E2 20 ethoxylated C10-2o alcohols, polyhydroxy fatty acid amide, and mixtures thereof. More preferred are C10 14 linear alkylbenzene sulfonate (most preferred), and E2 5 0 ethoxylated C12 18 alcohols.
1. Anionic Surfactant Anionic surfactants useful for detersive purposes are included in the compositions hereof. These can include salts of soap, Cg-C20 linear alkylbenzenesulphonates, Cg-C22 primary or secondary alkanesulphonates, Cg-C24 olefinsulphonates, sulphonated polycarboxylic acids prepared by sulphonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British Patent Specification No. 1,082,179, alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, paraffin sulfonates, alkyl phosphates, isothionates such as the acyl isothionates, N-acyl taurates, fatty acid amides of methyl tauride, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C12-C1g monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C6-C14 diesters), N-acyl sarcosinates (the nonionic nonsulfated compounds being described below), branched primary alkyl sulfates, alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH20)kCH2C00-M+ wherein R is a Cg-C22 alkyl, k is an integer from 0 to 10, and M is a soluble salt-forming cation, and fatty acids esterified with isothionic acid and neutralized with sodium hydroxide. Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil.
Further examples are given in ~Surface Active Agents and Detergents~ (Vol. I and II by Schwartz, Perry and Berch). A
variety of such surfactants are also generally disclosed in U.S.
Patent 3,929,678, issued December 30, 1975 to Laughlin, et al. at Column 23, line 58 through Column 29, line 23.
One type of anionic surfactant preferred for use in liquid detergent compositions herein is alkyl ester sulfonates, which is preferably alkyl ester sulfonate surfactant of the structural formula:
R3---cH-- e --oR4 wherein R3 is a C8-C20 hydrocarbyl, preferably an alkyl, or combination thereof, R4 is a Cl-C6 hydrocarbyl, preferably an alkyl, or combination thereof, and M is a soluble salt-forming cation. Suitable salts include metal salts such as sodium, potassium, and lithium salts. Preferably, R3 is C10-Cl6 alkyl, and R4 is methyl, ethyl or isopropyl. Especially preferred are the methyl ester sulfonates wherein R3 is Cl4-Cl6 alkyl.
Preferred for use in liquid detergent compositions herein is Cg-C20 linear alkylbenzene sulfonate (preferably sodium salts).
Preferably the nonionic surfactant is the condensation product of Cl0-C20 alcohol and between about 2 and about 20 moles of ethylene oxide per mole of alcohol ("E220 ethoxylated C10-C20 alcohol").
2. Nonionic Surfactant Suitable nonionic detergent surfactants are generally disclosed in U.S. Patent 3,929,678, Laughlin et al., issued December 30, 1975, at Column 13, line 14 through Column 16, line 6. Exemplary, non-limiting classes of useful nonionic surfactants are listed below.
1. The polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols.
2. The condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide. The alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
,~AY~
~- - 8 - 2 1 2 6 3 ~ 2 3. The condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol.
4. The condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine.
5. Semi-polar nonionic surfactants are a special category of nonionic surfactants which include water-soluble amine oxides containing one alkyl moiety of from about 10 to about 18 carbon o atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to about 3 carbon atoms.
6. Alkylpolysaccharides disclosed in U.S. Patent 4,565,647, Llenado, issued January 21, 1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
7. Fatty acid amide surfactants having the formula:
o Il R6 - C - N(R7)2 wherein R6 is an alkyl group containing from about 7 to about 21 (preferably from about 9 to about 17) carbon atoms and each R7 is selected from the group consisting of hydrogen, Cl-C4 alkyl, Cl-C4 hydroxyalkyl, and -(C2H40)XH where x varies from about 1 to about The polyhydroxy fatty acid amide surfactant component comprises compounds of the structural formula:
- 9 - 2 12 6~ 82 .~
O Rl Il I
(I) R2 - C - N - Z
wherein: Rl is C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof, preferably C1-C4 alkyl, more preferably C1 or C2 alkyl, most preferably Cl alkyl (i.e., methyl); and R2 is a Cs-C31 hydrocarbyl, preferably straight chain C7-Clg alkyl or alkenyl, more preferably straight chain Cg-C17 alkyl or alkenyl, most preferably straight chain Cll-Cls alkyl or 0 alkenyl, or mixtures thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z will be a glycityl. Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose. Z preferably will be selected from the group consisting of -CH2-(CHOH)n-CH20H, -CH(CH20H)-(CHOH)n 1-CH20H, -CH2-(CHOH)2(CHOR')(CHOH)-CH20H, and alkoxylated derivatives thereof, where n is an integer from 3 to 5, inclusive, and R' is H
or a cyclic or aliphatic monosaccharide. Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH20H.
C. pH JumD Svstem Solid, substantially water-insoluble peroxyacids are more stable at acidic pHs while cleaning and bleaching effectiveness of liquid laundry detergents in the wash is better at alkaline pHs.
Incorporation of peroxyacid bleaches in liquid laundry detergents, particularly heavy duty liquids, was therefore thought to be impractical. Attaining these different pH requirements in product and in the wash is accomplished by using a pH jump (i.e.
adjusting) system to maintain product pH between about 3 and about 6 and to achieve a pH in the wash (i.e. on dilution) of between about 7 and about 10.
The present composition comprises from about 2 to about 40%, preferably from about 5 to about 30%, most preferably from about 10 to about 25%, by weight of the composition, of a pH jump system which produces a pH in the composition of between about 3 and - lo - 2 1 2 6 3 ~ ~
about 6, preferably from about 3.5 to about 5, most preferably from about 4 to about 4.5, and upon dilution of the composition produces a pH of between about 7 and about 10, preferably from about 7.5 to about 9, in the dilute solution.
1. Borate/PolYol DH Jump SYstem Preferably, compositions of the present invention comprise from about 2 to about 40%, preferably from about 5 to about 30%, most preferably from about 10 to about 25%, by weight of the composition, of a pH jump system comprising:
1. a borate and;
2. a polyol wherein the polyol is a cis 1,2 polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause an increase in pH in the solution to a va~ue of about 7-9, the polyol to borate weight ratio being 1:1 to 10:1.
The present compositions most preferably comprise from about 1 to about 20%, preferably from about 2 to about 10%, by weight of the composition, of a boron compound such as borax (preferred), boric oxide, or sodium ortho- or pyro-borate; and from about 1 to about 20X, preferably from about 5 to about 15%, by weight of the composition, of a polyol such as sorbitol, dulcitol, xylitol, fructose, arabitol, mannitol, galactitol, catechol, pinacol, glucose and polyhydroxy fatty acid amide. Preferred polyols for use herein are sorbitol, xylitol and dulcitol. Most preferred compositions comprise from about 4 to about 6%, by weight of the composition, of borax and from about 10 to about 15%, by weight of the composition, of sorbitol.
Preferably, the polyol is dissolved in part of the water to be added to the formula, followed by the addition to this mixture of any salt or electrolytes in the formula. Last, the boron compound is mixed into this pre-mix. This clear pH jump solution is added to the remainder of the formula after the surfactants.
The mechanism of action of this borate-polyol system is believed to be the formation of an acidic borate-polyol complex in - ll - 2126382 concentrated solution. Upon dilution, the complex dissociates and yields borate ions, which have a buffered pH of about 9.
2. Other pH Jump SYstems Other pH jump systems aside from borate/polyol can be useful herein. These may include insoluble alkaline salts in product which dissolve in the wash for a more alkaline pH. These may include sodium carbonate, sodium bicarbonate, sodium silicate, sodium pyrophosphate and orthophosphate.
D. Xanthan polYsaccharide lo Compositions of the present invention comprise from about 0.05 to about 2%, preferably from about 0.1 to about 1%, most preferably from about 0.1 to about 0.15%, by weight of the composition, of agar or xanthan polysaccharide, which is also called xanthan gum. Xanthan gum is produced by fermentation and extraction of the naturally occurring plant bacteria, Xanthomonas campestrias.
E. Fattv Acid Preferred compositions for the second type of high nonionic surfactant composition comprise from about 0.5 to about 3.5%, preferably from about 1 to about 3%, most preferably from about 1.5 to about 2.5X, by weight of the composition, of C10-16, preferably C10-12, fatty acid. Preferred are lauric acid, myristic acid, palmitic acid, and stearic acid. Most preferred is lauric acid. These low levels of fatty acid are included for product phase stability.
F. Other Parameters The present aqueous laundry detergent compositions do not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer. The second type of composition (high nonionic surfactant) preferably does not include such a copolymer. Stability enhancing polymers in general need not be included herein.
The following are preferably not included in the present compositions: enzymes, an effective amount of detergency builder, urea, and glycerol. An effective amount of detergency builder is preferably more than about 4% and less than about 30X, by weight - 12 - 21~6382 of the composition (to exclude the above-described low fatty acid levels).
The compositions herein preferably have a viscosity of from about 100 to about 3000, most preferably from about 300 to about 1000, most preferably from about 400 to about 900, centipoise (cps) at 20-C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm. This viscosity is desirable for convenient pouring from a container by a liquid laundry detergent user.
G. ODtional Ingredients The ingredients herein should be combined in any manner which will evenly disperse or dissolve them in the composition, and which does not interfere with their action. The preferred order of addition is: surfactant, lauric acid, pH jump, electrolytes, chelant, peroxyacid, xanthan gum, polyacrylate, brightener, polyvinyl pyrrolidone and water to balance.
Optional and preferred ingredients include from about 0.5 to about 5, preferably from I to 2, % by weight of the composition of polyvinyl pyrrolidone (preferred) and/or polyvinyl alcohol. The PVP, which includes substituted and unsubstituted vinyl pyrrolidone polymerization products, and PVA have a molecular weight between about 4,000 and about 200,000, preferably between about 5,000 and about 100,000, most preferably between 10,000 and 30,000. A combination of PVPs and/or PVAs of different molecular weights could also be used.
Another optional and preferred ingredient is from about 0.05 to about 2, preferably from about 0.1 to 1, X by weight of the composition of bleach-stable, stilbene fluorescent whitening agent (~F~A~). This preferably has the following structural formula:
(S\3M)n ~ - CH = CH ~
Rl R2 Rl R2 m wherein Rl is hydrogen, halogen, alkyl, alkoxy or phenyl;
~ 7 ~
Rz is hydrogen or alkyl;
M is hydrogen, an alkali metal or ammonium ion;
n = 0-2, but the formula must contain at least one S03M group; and m = 1-2 and when m=1, the substituent on the linkage carbon is hydrogen.
Suitable stilbene FWAs for use herein, if they are bleach-stable, are as described in U.S. Patents 4,309,316 and 4,298,490, Lange et al, issued January 5, 1982 and November 3, 1981 respectively, and U.S.
Patent 5,035,825, Eckhardt et al, issued July 30, 1991.
0 The most preferred stilbene FWA for use herein, because it is bleach-stable, is Tinopal~ CBS-X, which is benzenesulfonic acid, 2,2'-((1,1'-biphenyl)-4,4'-diyldi-2,1-ethenediyl)bis-, disodium salt (CA
Index Name). The formula for Tinopal~ CBS-X is:
~ 3Na+ ~ N +
A sufficient amount of sodium hydroxide (0.4N) is added (usually 2-5 weight %) just before balancing with water to bring the pH of the composition at 20~C to a preferred pH of 4.5.
Hydrotropes such as sodium and potassium, xylene sulfonate, sodium and potassium toluene sulfonate, sodium and potassium sulfonate, and mixtures thereof, and related compounds (as disclosed in U.S. Patent 3,915,903) can be utilized in the compositions of the present invention.
They may be present at levels of from about 0.5% to about 10%, preferably from about 1% to about 5%, by weight.
Examples of suitable chelants for use herein are:
carboxylates, such as ethylene diamine tetraacetate (EDTA) and diethylene triamine pentaacetate (DTPA); polyphosphates, such as sodium acid pyrophosphate (SAPP), tetrasodium pyrophosphate (TSPP), and sodium tripolyphosphate (STPP); phosphonates, such as ethylhydroxydiphosphonate (Dequest~ 2010 (1-hydroxyethylidene) ,~
- 14 - 21263~2 bisphosphonic acid) and other sequestering agents sold under the Dequest~ trade name; and combinations of the above. Other sequestering agents for use herein are 2,6-pyridinedicarboxylic acid (dipicolinic acid), picolinic acid, and 8-hydroxyquinoline, and combinations thereof. From about 0.05 to about 0.5% of ethylhydroxydiphosphonate and dipicolinic acid, alone or combined, are preferred chelants.
The compositions herein may further contain magnesium sulfate, which is commercially available in the heptahydrate form.
(If anhydrous magnesium sulfate is used, the above levels should be adjusted accordingly.) The compositions may further contain sodium sulfate or potassium sulfate.
This invention further provides a method for cleaning and bleaching fabrics in the wash by contacting the fabrics with effective amounts of an aqueous liquid detergent composition comprising, by weight of the composition:
a. from about 1 to about 30X of solid, substantially water-insoluble organic peroxyacid;
b. from about 5 to about 50% of detergent surfactant;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; and which laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
Also provided is a method for cleaning and bleaching fabrics in the wash by contacting the fabrics with effective amounts of an aqueous liquid laundry detergent composition comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
~ - 15 - 21263~2 b. from about 10 to about 40% of C8-20 alcohol which has been ethoxylated with an average of from about 2 to about 20 moles of ethylene oxide per mole of alcohol;
c. from 0 to about 10% of bleach-compatible anionic surfactant; and d. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution;
e. from about 0.05 to about 2% of agar or xanthan polysaccharide; and f. from about 0.5 to about 3% of C10-14 fatty acid.
The following examples illustrate the compositions of the present invention. All parts, percentages and ratios used herein are by weight unless otherwise specified.
EXAMPLE I
A composition of the present invention is as follows.
~ngredient Active %
C12-15 alkylethoxylate (E9) 5.2 C12-13 linear alkylbenzene sulfonic acid 12.1 Monononylamido peroxyadipic acid 1.6 Ethylhydroxydiphosphonate 0.2 Magnesium sulfate heptahydrate 2.25 Sodium sulfate 2.25 Sorbitol 10.5 Borax 3. 8 Xanthan gum 0.10 Sodium polyacrylate (MW 10,000) 0.15 Fluorescent whitening agent (nFWA~) 0.30 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 800 centipoise (cps)--pourable pH jump: 4.38 (product); 8.00 (wash solution) - - 16 - ~26382 The procedure for the preparation of the above composition containing peroxyacid bleach is as follows:
1. Xanthan gum is dissolved in enough water to make a 1%
solution.
2. A pH jump premix is prepared by dissolving the sorbitol and borax in an equal amount of water. If any electrolytes are in the composition, they can also be dissolved in the pH jump premix.
3. The composition is prepared in an appropriate size beaker (typically a 2-liter beaker). First charge the beaker with the linear alkyl benzene sulfonic acid, alkylethoxylate and, if present, lauric acid, and mix to dissolve.
4. The pH jump premix is added to the stirring surfactant mix.
5. The chelant is added with agitation.
6. The desired amount of solid peroxyacid (e.g. NAPM ) is added and dispersed.
7. The xanthan gum solution is added.
o Il R6 - C - N(R7)2 wherein R6 is an alkyl group containing from about 7 to about 21 (preferably from about 9 to about 17) carbon atoms and each R7 is selected from the group consisting of hydrogen, Cl-C4 alkyl, Cl-C4 hydroxyalkyl, and -(C2H40)XH where x varies from about 1 to about The polyhydroxy fatty acid amide surfactant component comprises compounds of the structural formula:
- 9 - 2 12 6~ 82 .~
O Rl Il I
(I) R2 - C - N - Z
wherein: Rl is C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof, preferably C1-C4 alkyl, more preferably C1 or C2 alkyl, most preferably Cl alkyl (i.e., methyl); and R2 is a Cs-C31 hydrocarbyl, preferably straight chain C7-Clg alkyl or alkenyl, more preferably straight chain Cg-C17 alkyl or alkenyl, most preferably straight chain Cll-Cls alkyl or 0 alkenyl, or mixtures thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z will be a glycityl. Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose. Z preferably will be selected from the group consisting of -CH2-(CHOH)n-CH20H, -CH(CH20H)-(CHOH)n 1-CH20H, -CH2-(CHOH)2(CHOR')(CHOH)-CH20H, and alkoxylated derivatives thereof, where n is an integer from 3 to 5, inclusive, and R' is H
or a cyclic or aliphatic monosaccharide. Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH20H.
C. pH JumD Svstem Solid, substantially water-insoluble peroxyacids are more stable at acidic pHs while cleaning and bleaching effectiveness of liquid laundry detergents in the wash is better at alkaline pHs.
Incorporation of peroxyacid bleaches in liquid laundry detergents, particularly heavy duty liquids, was therefore thought to be impractical. Attaining these different pH requirements in product and in the wash is accomplished by using a pH jump (i.e.
adjusting) system to maintain product pH between about 3 and about 6 and to achieve a pH in the wash (i.e. on dilution) of between about 7 and about 10.
The present composition comprises from about 2 to about 40%, preferably from about 5 to about 30%, most preferably from about 10 to about 25%, by weight of the composition, of a pH jump system which produces a pH in the composition of between about 3 and - lo - 2 1 2 6 3 ~ ~
about 6, preferably from about 3.5 to about 5, most preferably from about 4 to about 4.5, and upon dilution of the composition produces a pH of between about 7 and about 10, preferably from about 7.5 to about 9, in the dilute solution.
1. Borate/PolYol DH Jump SYstem Preferably, compositions of the present invention comprise from about 2 to about 40%, preferably from about 5 to about 30%, most preferably from about 10 to about 25%, by weight of the composition, of a pH jump system comprising:
1. a borate and;
2. a polyol wherein the polyol is a cis 1,2 polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause an increase in pH in the solution to a va~ue of about 7-9, the polyol to borate weight ratio being 1:1 to 10:1.
The present compositions most preferably comprise from about 1 to about 20%, preferably from about 2 to about 10%, by weight of the composition, of a boron compound such as borax (preferred), boric oxide, or sodium ortho- or pyro-borate; and from about 1 to about 20X, preferably from about 5 to about 15%, by weight of the composition, of a polyol such as sorbitol, dulcitol, xylitol, fructose, arabitol, mannitol, galactitol, catechol, pinacol, glucose and polyhydroxy fatty acid amide. Preferred polyols for use herein are sorbitol, xylitol and dulcitol. Most preferred compositions comprise from about 4 to about 6%, by weight of the composition, of borax and from about 10 to about 15%, by weight of the composition, of sorbitol.
Preferably, the polyol is dissolved in part of the water to be added to the formula, followed by the addition to this mixture of any salt or electrolytes in the formula. Last, the boron compound is mixed into this pre-mix. This clear pH jump solution is added to the remainder of the formula after the surfactants.
The mechanism of action of this borate-polyol system is believed to be the formation of an acidic borate-polyol complex in - ll - 2126382 concentrated solution. Upon dilution, the complex dissociates and yields borate ions, which have a buffered pH of about 9.
2. Other pH Jump SYstems Other pH jump systems aside from borate/polyol can be useful herein. These may include insoluble alkaline salts in product which dissolve in the wash for a more alkaline pH. These may include sodium carbonate, sodium bicarbonate, sodium silicate, sodium pyrophosphate and orthophosphate.
D. Xanthan polYsaccharide lo Compositions of the present invention comprise from about 0.05 to about 2%, preferably from about 0.1 to about 1%, most preferably from about 0.1 to about 0.15%, by weight of the composition, of agar or xanthan polysaccharide, which is also called xanthan gum. Xanthan gum is produced by fermentation and extraction of the naturally occurring plant bacteria, Xanthomonas campestrias.
E. Fattv Acid Preferred compositions for the second type of high nonionic surfactant composition comprise from about 0.5 to about 3.5%, preferably from about 1 to about 3%, most preferably from about 1.5 to about 2.5X, by weight of the composition, of C10-16, preferably C10-12, fatty acid. Preferred are lauric acid, myristic acid, palmitic acid, and stearic acid. Most preferred is lauric acid. These low levels of fatty acid are included for product phase stability.
F. Other Parameters The present aqueous laundry detergent compositions do not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer. The second type of composition (high nonionic surfactant) preferably does not include such a copolymer. Stability enhancing polymers in general need not be included herein.
The following are preferably not included in the present compositions: enzymes, an effective amount of detergency builder, urea, and glycerol. An effective amount of detergency builder is preferably more than about 4% and less than about 30X, by weight - 12 - 21~6382 of the composition (to exclude the above-described low fatty acid levels).
The compositions herein preferably have a viscosity of from about 100 to about 3000, most preferably from about 300 to about 1000, most preferably from about 400 to about 900, centipoise (cps) at 20-C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm. This viscosity is desirable for convenient pouring from a container by a liquid laundry detergent user.
G. ODtional Ingredients The ingredients herein should be combined in any manner which will evenly disperse or dissolve them in the composition, and which does not interfere with their action. The preferred order of addition is: surfactant, lauric acid, pH jump, electrolytes, chelant, peroxyacid, xanthan gum, polyacrylate, brightener, polyvinyl pyrrolidone and water to balance.
Optional and preferred ingredients include from about 0.5 to about 5, preferably from I to 2, % by weight of the composition of polyvinyl pyrrolidone (preferred) and/or polyvinyl alcohol. The PVP, which includes substituted and unsubstituted vinyl pyrrolidone polymerization products, and PVA have a molecular weight between about 4,000 and about 200,000, preferably between about 5,000 and about 100,000, most preferably between 10,000 and 30,000. A combination of PVPs and/or PVAs of different molecular weights could also be used.
Another optional and preferred ingredient is from about 0.05 to about 2, preferably from about 0.1 to 1, X by weight of the composition of bleach-stable, stilbene fluorescent whitening agent (~F~A~). This preferably has the following structural formula:
(S\3M)n ~ - CH = CH ~
Rl R2 Rl R2 m wherein Rl is hydrogen, halogen, alkyl, alkoxy or phenyl;
~ 7 ~
Rz is hydrogen or alkyl;
M is hydrogen, an alkali metal or ammonium ion;
n = 0-2, but the formula must contain at least one S03M group; and m = 1-2 and when m=1, the substituent on the linkage carbon is hydrogen.
Suitable stilbene FWAs for use herein, if they are bleach-stable, are as described in U.S. Patents 4,309,316 and 4,298,490, Lange et al, issued January 5, 1982 and November 3, 1981 respectively, and U.S.
Patent 5,035,825, Eckhardt et al, issued July 30, 1991.
0 The most preferred stilbene FWA for use herein, because it is bleach-stable, is Tinopal~ CBS-X, which is benzenesulfonic acid, 2,2'-((1,1'-biphenyl)-4,4'-diyldi-2,1-ethenediyl)bis-, disodium salt (CA
Index Name). The formula for Tinopal~ CBS-X is:
~ 3Na+ ~ N +
A sufficient amount of sodium hydroxide (0.4N) is added (usually 2-5 weight %) just before balancing with water to bring the pH of the composition at 20~C to a preferred pH of 4.5.
Hydrotropes such as sodium and potassium, xylene sulfonate, sodium and potassium toluene sulfonate, sodium and potassium sulfonate, and mixtures thereof, and related compounds (as disclosed in U.S. Patent 3,915,903) can be utilized in the compositions of the present invention.
They may be present at levels of from about 0.5% to about 10%, preferably from about 1% to about 5%, by weight.
Examples of suitable chelants for use herein are:
carboxylates, such as ethylene diamine tetraacetate (EDTA) and diethylene triamine pentaacetate (DTPA); polyphosphates, such as sodium acid pyrophosphate (SAPP), tetrasodium pyrophosphate (TSPP), and sodium tripolyphosphate (STPP); phosphonates, such as ethylhydroxydiphosphonate (Dequest~ 2010 (1-hydroxyethylidene) ,~
- 14 - 21263~2 bisphosphonic acid) and other sequestering agents sold under the Dequest~ trade name; and combinations of the above. Other sequestering agents for use herein are 2,6-pyridinedicarboxylic acid (dipicolinic acid), picolinic acid, and 8-hydroxyquinoline, and combinations thereof. From about 0.05 to about 0.5% of ethylhydroxydiphosphonate and dipicolinic acid, alone or combined, are preferred chelants.
The compositions herein may further contain magnesium sulfate, which is commercially available in the heptahydrate form.
(If anhydrous magnesium sulfate is used, the above levels should be adjusted accordingly.) The compositions may further contain sodium sulfate or potassium sulfate.
This invention further provides a method for cleaning and bleaching fabrics in the wash by contacting the fabrics with effective amounts of an aqueous liquid detergent composition comprising, by weight of the composition:
a. from about 1 to about 30X of solid, substantially water-insoluble organic peroxyacid;
b. from about 5 to about 50% of detergent surfactant;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; and which laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer.
Also provided is a method for cleaning and bleaching fabrics in the wash by contacting the fabrics with effective amounts of an aqueous liquid laundry detergent composition comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
~ - 15 - 21263~2 b. from about 10 to about 40% of C8-20 alcohol which has been ethoxylated with an average of from about 2 to about 20 moles of ethylene oxide per mole of alcohol;
c. from 0 to about 10% of bleach-compatible anionic surfactant; and d. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution;
e. from about 0.05 to about 2% of agar or xanthan polysaccharide; and f. from about 0.5 to about 3% of C10-14 fatty acid.
The following examples illustrate the compositions of the present invention. All parts, percentages and ratios used herein are by weight unless otherwise specified.
EXAMPLE I
A composition of the present invention is as follows.
~ngredient Active %
C12-15 alkylethoxylate (E9) 5.2 C12-13 linear alkylbenzene sulfonic acid 12.1 Monononylamido peroxyadipic acid 1.6 Ethylhydroxydiphosphonate 0.2 Magnesium sulfate heptahydrate 2.25 Sodium sulfate 2.25 Sorbitol 10.5 Borax 3. 8 Xanthan gum 0.10 Sodium polyacrylate (MW 10,000) 0.15 Fluorescent whitening agent (nFWA~) 0.30 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 800 centipoise (cps)--pourable pH jump: 4.38 (product); 8.00 (wash solution) - - 16 - ~26382 The procedure for the preparation of the above composition containing peroxyacid bleach is as follows:
1. Xanthan gum is dissolved in enough water to make a 1%
solution.
2. A pH jump premix is prepared by dissolving the sorbitol and borax in an equal amount of water. If any electrolytes are in the composition, they can also be dissolved in the pH jump premix.
3. The composition is prepared in an appropriate size beaker (typically a 2-liter beaker). First charge the beaker with the linear alkyl benzene sulfonic acid, alkylethoxylate and, if present, lauric acid, and mix to dissolve.
4. The pH jump premix is added to the stirring surfactant mix.
5. The chelant is added with agitation.
6. The desired amount of solid peroxyacid (e.g. NAPM ) is added and dispersed.
7. The xanthan gum solution is added.
8. Next the sodium polyacrylate is added.
9. Then the fluorescent whitening agent, and PVP, if present, is added.
10. The resulting mix is homogenized on a homogenizer at low speed for about 1 minute.
11. The pH of the composition is adjusted to 4.5 with a 4N
sodium hydroxide solution.
The resulting product is a pourable, creamy suspension. The pH jump capability of the composition is checked by diluting 1.5 gm. of the composition into 1,000 gms. of water.
In the above formula, other peroxyacids can be substituted for the monononylamido peroxyadipic acid, such as 1,12-diperoxy-dodecanedioic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan polysaccharide. Other detergent surfactants can be substituted for the above. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
- 17 - 2~2~3~
EXAMPLE II
A composition of the present invention containing 1,12-diperoxydodecanedioic acid as the peroxyacid is as follows.
The procedure for preparation is as described in Example I.
Ingredient Active %
C12-13 alkylethoxylate (E6. 5) 12 . 1 C12 linear alkylbenzene sulfonic acid 5.2 1, 12 - Diperoxydodecanedioic acid 2 Dipicolinic acid 0.3 0 Magnesium sulfate heptahydrate 6.8 Sodium sulfate 5.38 Sorbitol 10.6 Borax 2 . 4 Lauric acid 2.5 Xanthan gum 0.12 Sodium polyacrylate (MW 10,000) 0.1 FWA 0.1 Polyvinyl pyrrolidone (MW 10,000) 1.0 Sodium hydroxide (4N) 2.0 Water Balance Viscosity: 430 centipoise pH jump: 4.5 (product) to 7.78 (wash) In the above formula, other peroxyacids can be substituted for the 1,12-diperoxydodecanedioic acid, such as monononylamido peroxyadipic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan gum. Other detergent surfactants can be substituted for the above. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
EXAMPLE III
A composition of the present (high nonionic surfactant) invention containing 1,12-diperoxydodecanedioic acid as the peroxyacid is as follows.
- 18 - 2126~8~
Inqredient Active %
C12-13 alkylethoxylate (E6-5) 15 Linear alkylbenzene sulfonic acid 5.2 1,12-Diperoxydodecanedioic acid 2 Dipicolinic acid 0.3 Magnesium sulfate heptahydrate 4.2 Sorbitol 14.1 Borax 5.1 Lauric acid 2.0 lo Xanthan gum 0.12 Sodium polyacrylate 0.25 FWA 0.20 Polyvinyl pyrrolidone (MW 4,500) 1.0 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 660 centipoise pH jump: 4.5 (product) to 7.85 (wash) In the above formula, other peroxyacids can be substituted for the 1,12-diperoxydodecanedioic acid, such as monononylamido peroxyadipic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan gum. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
EXAMPLE IV
A composltion of the present invention (high nonionic 30 surfactant) is as follows. The procedure for preparation is as described in Example I.
Ingredient Active %
C12-15 alkylethoxylate (E9) 15 C12 linear alkylbenzene sulfonic acid 6.4 Monononylamido peroxyadipic acid 2 Ethylhydroxydiphosphonate 0.2 Magnesium sulfate heptahydrate 6.0 - 19 - 2 l 2 63 8~
,~
Sorbitol 20 Borax 5 0 Lauric acid 2.0 Xanthan gum 0.15 Sodium polyacrylate (MW 4,500) 0.20 FWA 0.20 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 910 centipoise (cps) pH Jump: 4.5 (product) to 7.95 (wash)
sodium hydroxide solution.
The resulting product is a pourable, creamy suspension. The pH jump capability of the composition is checked by diluting 1.5 gm. of the composition into 1,000 gms. of water.
In the above formula, other peroxyacids can be substituted for the monononylamido peroxyadipic acid, such as 1,12-diperoxy-dodecanedioic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan polysaccharide. Other detergent surfactants can be substituted for the above. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
- 17 - 2~2~3~
EXAMPLE II
A composition of the present invention containing 1,12-diperoxydodecanedioic acid as the peroxyacid is as follows.
The procedure for preparation is as described in Example I.
Ingredient Active %
C12-13 alkylethoxylate (E6. 5) 12 . 1 C12 linear alkylbenzene sulfonic acid 5.2 1, 12 - Diperoxydodecanedioic acid 2 Dipicolinic acid 0.3 0 Magnesium sulfate heptahydrate 6.8 Sodium sulfate 5.38 Sorbitol 10.6 Borax 2 . 4 Lauric acid 2.5 Xanthan gum 0.12 Sodium polyacrylate (MW 10,000) 0.1 FWA 0.1 Polyvinyl pyrrolidone (MW 10,000) 1.0 Sodium hydroxide (4N) 2.0 Water Balance Viscosity: 430 centipoise pH jump: 4.5 (product) to 7.78 (wash) In the above formula, other peroxyacids can be substituted for the 1,12-diperoxydodecanedioic acid, such as monononylamido peroxyadipic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan gum. Other detergent surfactants can be substituted for the above. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
EXAMPLE III
A composition of the present (high nonionic surfactant) invention containing 1,12-diperoxydodecanedioic acid as the peroxyacid is as follows.
- 18 - 2126~8~
Inqredient Active %
C12-13 alkylethoxylate (E6-5) 15 Linear alkylbenzene sulfonic acid 5.2 1,12-Diperoxydodecanedioic acid 2 Dipicolinic acid 0.3 Magnesium sulfate heptahydrate 4.2 Sorbitol 14.1 Borax 5.1 Lauric acid 2.0 lo Xanthan gum 0.12 Sodium polyacrylate 0.25 FWA 0.20 Polyvinyl pyrrolidone (MW 4,500) 1.0 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 660 centipoise pH jump: 4.5 (product) to 7.85 (wash) In the above formula, other peroxyacids can be substituted for the 1,12-diperoxydodecanedioic acid, such as monononylamido peroxyadipic acid or sulfone peroxyacid or phthaloyl amino-peroxycaproic acid. Agar polysaccharide can be substituted for the xanthan gum. Water can replace magnesium sulfate heptahydrate and sodium sulfate in the above formula.
EXAMPLE IV
A composltion of the present invention (high nonionic 30 surfactant) is as follows. The procedure for preparation is as described in Example I.
Ingredient Active %
C12-15 alkylethoxylate (E9) 15 C12 linear alkylbenzene sulfonic acid 6.4 Monononylamido peroxyadipic acid 2 Ethylhydroxydiphosphonate 0.2 Magnesium sulfate heptahydrate 6.0 - 19 - 2 l 2 63 8~
,~
Sorbitol 20 Borax 5 0 Lauric acid 2.0 Xanthan gum 0.15 Sodium polyacrylate (MW 4,500) 0.20 FWA 0.20 Sodium hydroxide (4N) to pH 4.5 Water Balance Viscosity: 910 centipoise (cps) pH Jump: 4.5 (product) to 7.95 (wash)
Claims (20)
1. A stable, pourable aqueous liquid laundry detergent composition comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially, water-insoluble organic peroxyacid:
b. from about 10 to about 40% of detergent surfactant selected from anionic surfactants and mixtures of anionic and nonionic surfactants with a ratio of nonionic to anionic that is not greater than 1:1;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; wherein said laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer; and wherein said laundry detergent composition has a viscosity of from about 100 to about 3,000 cps at 20°C when measured with an RVT Brookfield Viscometer, using No. 3 spindle and a setting of 100 rpm.
a. from about 1 to about 30% of solid, substantially, water-insoluble organic peroxyacid:
b. from about 10 to about 40% of detergent surfactant selected from anionic surfactants and mixtures of anionic and nonionic surfactants with a ratio of nonionic to anionic that is not greater than 1:1;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; wherein said laundry detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer; and wherein said laundry detergent composition has a viscosity of from about 100 to about 3,000 cps at 20°C when measured with an RVT Brookfield Viscometer, using No. 3 spindle and a setting of 100 rpm.
2. A stable, pourable aqueous liquid laundry detergent composition according to Claim 1, comprising from about 0.1 to about 1% of xanthan polysaccharide.
3. A stable, pourable aqueous liquid laundry detergent composition according to Claim 2, comprising from about 1 to about 20% of solid, substantially water-insoluble organic peroxyacid selected from the group consisting of 4-nonylamino-4-oxoperoxybutyric acid; 6-nonylamino-6-oxoperoxyhexanoic acid; heptyl sulfonylperpropionic acid; decylsulphonyl perpropionic acid; heptyl-, octyl-, nonyl-, and decylsulphonyl-perbutyric acid; 1,12-diperoxydodecanedioic acid; and phthaloyl aminoperoxycaproic acid.
4. A stable, pourable aqueous liquid laundry detergent composition according to Claim 2, comprising from about 30 to about 70%, by weight of the composition, of distilled, deionized water.
5. A stable, pourable aqueous liquid laundry detergent composition according to Claim 4, comprising from about 10 to about 25% of a pH jump system which produces a pH in the composition of between about 3.5 and about 5, and upon dilution of the composition produces a pH of between about 7.5 and about 9 in the dilute solution.
6. A stable, pourable aqueous liquid laundry detergent composition according to Claim 4, comprising from about 1.5 to about 5% of monononanoylamido peroxyadipic acid or 1,2-diperoxydodecanedioic acid.
7. A stable, pourable aqueous liquid laundry detergent composition according to Claim 2, comprising from about 0.1 to about 0.5% of xanthan polysaccharide.
8. A stable, pourable aqueous liquid laundry detergent composition according to Claim 7, comprising from about 2 to about 40% of a pH jump system comprising:
1. a borate and;
2. a polyol wherein the polyol is a cis-1,2-polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause in increase in pH in the solution to a value of about 7-10, the polyol to borate weight ratio being 1:1 to 10:1.
1. a borate and;
2. a polyol wherein the polyol is a cis-1,2-polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause in increase in pH in the solution to a value of about 7-10, the polyol to borate weight ratio being 1:1 to 10:1.
9. A stable, pourable aqueous liquid laundry detergent composition according to Claim 8, comprising from about 15 to about 30% of nonionic and anionic detergent surfactant.
10. A stable, pourable aqueous liquid laundry detergent composition according to Claim 7, comprising from about 1.5 to about 5% of monononanoylamido peroxyadipic acid.
11. A stable, pourable aqueous liquid laundry detergent composition according to Claim 10, comprising from about 5 to about 30% of a pH
adjusting system comprising:
1. a borate and;
2. a polyol wherein the polyol is a cis-1,2-polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause in increase in pH in the solution to a value of about 7-10, the polyol to borate weight ratio being 1:1 to 10:1.
adjusting system comprising:
1. a borate and;
2. a polyol wherein the polyol is a cis-1,2-polyol capable of forming a complex with the borate when the composition is in a concentrated form to cause a reduction in pH of the composition to a value of about 3-6 and the complex being capable upon dilution of the composition, of dissociating in dilute solution to liberate the borate to cause in increase in pH in the solution to a value of about 7-10, the polyol to borate weight ratio being 1:1 to 10:1.
12. A stable, pourable aqueous liquid laundry detergent composition according to Claim 11, comprising from about 40 to about 60%, by weight of the composition, of distilled, deionized water.
13. A stable, pourable aqueous liquid laundry detergent composition according to Claim 12, having a viscosity of from about 300 to about 1,000 cps at 20°C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm.
14. A stable, pourable aqueous liquid laundry detergent composition according to Claim 13, comprising from about 1 to about 20%, by weight of the composition, of a boron compound selected from the group consisting of borax, boric oxide, sodium orthoborate and sodium pyroborate; and from about 1 to about 20%, by weight of the composition, of a polyol selected from the group consisting of sorbitol, dulcitol, xylitol, xarabitol, manitol, fructose, galactitol, catechol, pinacol, glucose and polyhydroxy fatty acid amide.
15. A stable, pourable aqueous liquid laundry detergent composition according to Claim 14, comprising from about 1 to about 3%, by weight of the composition, of C10-C12 fatty acid.
16. A stable, pourable aqueous liquid laundry detergent composition according to Claim 15, comprising from about 3 to about 6%, by weight of the composition, of borax and from about 10 to about 15%, by weight of the composition, of sorbitol.
17. A stable, pourable aqueous liquid laundry detergent composition according to Claim 16, having a viscosity of from about 400 to about 900 cps at 20°C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm.
18. A stable, pourable aqueous liquid laundry detergent composition according to Claim 17, comprising from about 0.05 to about 0.5% of ethylhydroxydiphosphonate.
19. A stable, pourable aqueous liquid laundry detergent composition according to Claim 15, and excluding enzymes and an effective amount of detergency builder.
20. A method for cleaning and bleaching fabrics in the wash by contacting the fabrics with a dilute solution formed from an effective amount of an aqueous liquid detergent composition comprising, by weight of the composition:
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
b. from about 10 to about 40% of detergent surfactant selected from anionic surfactants and mixtures of anionic and nonionic surfactants with a ratio of nonionic to anionic that is not greater than 1:1;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; wherein said detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer; and wherein said detergent composition has a viscosity from about 100 to about 3,000 cps at 20°C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm.
a. from about 1 to about 30% of solid, substantially water-insoluble organic peroxyacid;
b. from about 10 to about 40% of detergent surfactant selected from anionic surfactants and mixtures of anionic and nonionic surfactants with a ratio of nonionic to anionic that is not greater than 1:1;
c. from about 2 to about 40% of a pH jump system which produces a pH in the composition of between about 3 and about 6, and upon dilution of the composition produces a pH of between about 7 and about 10 in the dilute solution; and d. from about 0.05 to about 2% of agar or xanthan polysaccharide; wherein said detergent composition does not comprise a stability enhancing polymer which is a copolymer of a hydrophobic and a hydrophilic monomer; and wherein said detergent composition has a viscosity from about 100 to about 3,000 cps at 20°C when measured with an RVT Brookfield Viscometer, using a No. 3 spindle and a setting of 100 rpm.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8585793A | 1993-06-30 | 1993-06-30 | |
| US085,857 | 1993-06-30 |
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| Publication Number | Publication Date |
|---|---|
| CA2126382A1 CA2126382A1 (en) | 1994-12-31 |
| CA2126382C true CA2126382C (en) | 1998-12-15 |
Family
ID=22194432
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2126382 Expired - Fee Related CA2126382C (en) | 1993-06-30 | 1994-06-21 | Stable pourable aqueous liquid laundry detergent compositions with peroxyacid bleach |
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| Country | Link |
|---|---|
| JP (1) | JPH0770593A (en) |
| CA (1) | CA2126382C (en) |
| GB (1) | GB2281744A (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19824708A1 (en) * | 1998-06-03 | 1999-12-09 | Henkel Kgaa | Structurally viscous aqueous bleach |
| WO2000027967A1 (en) * | 1998-11-10 | 2000-05-18 | The Procter & Gamble Company | Bleaching compositions |
| WO2000027977A1 (en) * | 1998-11-10 | 2000-05-18 | The Procter & Gamble Company | Bleaching compositions |
| US6440921B1 (en) * | 1998-11-10 | 2002-08-27 | The Procter & Gamble Company | Bleaching compositions |
| DE19853845A1 (en) * | 1998-11-23 | 2000-05-25 | Henkel Kgaa | Viscous liquid aqueous bleach or laundry detergent concentrate containing hydrogen peroxide and surfactant is thickened with magnesium salt of mineral acid |
| GB9901957D0 (en) * | 1999-01-29 | 1999-03-17 | Yplon S A | Cleaning formulation |
| EP1631653B1 (en) * | 2003-06-09 | 2007-04-04 | Unilever Plc | Liquid bleaching composition |
| EP1616936A1 (en) * | 2004-07-16 | 2006-01-18 | Unilever N.V. | Liquid bleaching composition |
| JP4577884B2 (en) * | 2004-11-19 | 2010-11-10 | 花王株式会社 | Liquid detergent composition |
| JP4509746B2 (en) * | 2004-11-19 | 2010-07-21 | 花王株式会社 | Liquid bleach composition |
| JP5234557B2 (en) * | 2005-08-05 | 2013-07-10 | 花王株式会社 | Liquid bleach composition |
| DE102005063180A1 (en) * | 2005-12-30 | 2007-07-05 | Henkel Kgaa | Aqueous surfactant- and bleaching agent containing liquid washing or cleaning agent, comprises particulate peroxycarboxylic acid, preferably phthalimidoperoxohexanoic acid and magnesium sulfate |
| JP5291861B2 (en) * | 2006-01-27 | 2013-09-18 | 花王株式会社 | Liquid detergent composition |
| JP4855140B2 (en) * | 2006-05-18 | 2012-01-18 | 花王株式会社 | Liquid bleach detergent composition |
| JP5079258B2 (en) * | 2006-05-18 | 2012-11-21 | 花王株式会社 | Liquid bleach composition |
| JP5095125B2 (en) * | 2006-05-18 | 2012-12-12 | 花王株式会社 | Liquid detergent composition |
| JP5412040B2 (en) | 2008-02-08 | 2014-02-12 | 花王株式会社 | Liquid bleach composition |
| US8871807B2 (en) | 2008-03-28 | 2014-10-28 | Ecolab Usa Inc. | Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids |
| US8034759B2 (en) * | 2008-10-31 | 2011-10-11 | Ecolab Usa Inc. | Enhanced stability peracid compositions |
| DE102009027812A1 (en) | 2009-07-17 | 2011-01-20 | Henkel Ag & Co. Kgaa | Liquid washing or cleaning agent with graying-inhibiting polymer |
| GB2496132A (en) * | 2011-10-31 | 2013-05-08 | Reckitt Benckiser Nv | Pthalimidopercaproic acid sugar suspension |
| US9321664B2 (en) | 2011-12-20 | 2016-04-26 | Ecolab Usa Inc. | Stable percarboxylic acid compositions and uses thereof |
| CA2867565C (en) | 2012-03-30 | 2021-01-19 | Victor KEASLER | Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water |
| US20140256811A1 (en) | 2013-03-05 | 2014-09-11 | Ecolab Usa Inc. | Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids |
| US8822719B1 (en) | 2013-03-05 | 2014-09-02 | Ecolab Usa Inc. | Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring |
| US10165774B2 (en) | 2013-03-05 | 2019-01-01 | Ecolab Usa Inc. | Defoamer useful in a peracid composition with anionic surfactants |
| DE102018123920A1 (en) * | 2018-09-27 | 2020-04-02 | Buck Service Gmbh | Laundry detergents |
| US12096768B2 (en) | 2019-08-07 | 2024-09-24 | Ecolab Usa Inc. | Polymeric and solid-supported chelators for stabilization of peracid-containing compositions |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3709348A1 (en) * | 1987-03-21 | 1988-10-06 | Degussa | PEROXYCARBONIC ACID CONTAINING AQUEOUS FLEMING SOLUTIONS, METHOD FOR THEIR PRODUCTION AND THEIR USE |
| US4992194A (en) * | 1989-06-12 | 1991-02-12 | Lever Brothers Company, Division Of Conopco Inc. | Stably suspended organic peroxy bleach in a structured aqueous liquid |
-
1994
- 1994-06-21 CA CA 2126382 patent/CA2126382C/en not_active Expired - Fee Related
- 1994-06-29 JP JP6147929A patent/JPH0770593A/en active Pending
- 1994-06-30 GB GB9413192A patent/GB2281744A/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| GB2281744A (en) | 1995-03-15 |
| GB9413192D0 (en) | 1994-08-24 |
| JPH0770593A (en) | 1995-03-14 |
| CA2126382A1 (en) | 1994-12-31 |
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| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |