EP1645619A1 - Liquid Detergent Compositions - Google Patents
Liquid Detergent Compositions Download PDFInfo
- Publication number
- EP1645619A1 EP1645619A1 EP05020855A EP05020855A EP1645619A1 EP 1645619 A1 EP1645619 A1 EP 1645619A1 EP 05020855 A EP05020855 A EP 05020855A EP 05020855 A EP05020855 A EP 05020855A EP 1645619 A1 EP1645619 A1 EP 1645619A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition according
- alkyl
- weight
- alcohol
- surfactants
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 45
- 239000007788 liquid Substances 0.000 title claims abstract description 29
- 239000003599 detergent Substances 0.000 title claims abstract description 25
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- -1 alkenyl ether Chemical compound 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 150000002191 fatty alcohols Chemical class 0.000 claims description 17
- 239000000344 soap Substances 0.000 claims description 17
- 239000004094 surface-active agent Substances 0.000 claims description 12
- 239000002736 nonionic surfactant Substances 0.000 claims description 11
- 229930182470 glycoside Natural products 0.000 claims description 9
- 150000002338 glycosides Chemical class 0.000 claims description 9
- 239000003093 cationic surfactant Substances 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 239000004665 cationic fabric softener Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 125000005131 dialkylammonium group Chemical group 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- 235000014113 dietary fatty acids Nutrition 0.000 description 13
- 229930195729 fatty acid Natural products 0.000 description 13
- 239000000194 fatty acid Substances 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 9
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 9
- 229920000151 polyglycol Polymers 0.000 description 8
- 239000010695 polyglycol Substances 0.000 description 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 6
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 6
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 150000002170 ethers Chemical class 0.000 description 6
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- 239000013543 active substance Substances 0.000 description 4
- 235000008504 concentrate Nutrition 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 4
- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 3
- DJYWKXYRGAMLRE-QXMHVHEDSA-N (z)-icos-9-en-1-ol Chemical compound CCCCCCCCCC\C=C/CCCCCCCCO DJYWKXYRGAMLRE-QXMHVHEDSA-N 0.000 description 3
- CFOQKXQWGLAKSK-UHFFFAOYSA-N 13-docosen-1-ol Natural products CCCCCCCCC=CCCCCCCCCCCCCO CFOQKXQWGLAKSK-UHFFFAOYSA-N 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 239000004435 Oxo alcohol Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229960000541 cetyl alcohol Drugs 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229960000735 docosanol Drugs 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 229940043348 myristyl alcohol Drugs 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- ALSTYHKOOCGGFT-MDZDMXLPSA-N oleyl alcohol Chemical compound CCCCCCCC\C=C\CCCCCCCCO ALSTYHKOOCGGFT-MDZDMXLPSA-N 0.000 description 3
- 229940055577 oleyl alcohol Drugs 0.000 description 3
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- TVPWKOCQOFBNML-SEYXRHQNSA-N (z)-octadec-6-en-1-ol Chemical compound CCCCCCCCCCC\C=C/CCCCCO TVPWKOCQOFBNML-SEYXRHQNSA-N 0.000 description 2
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000019635 sulfation Effects 0.000 description 2
- 238000005670 sulfation reaction Methods 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- IKYKEVDKGZYRMQ-PDBXOOCHSA-N (9Z,12Z,15Z)-octadecatrien-1-ol Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCCO IKYKEVDKGZYRMQ-PDBXOOCHSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- RRBZUCWNYQUCTR-UHFFFAOYSA-N 2-(aminoazaniumyl)acetate Chemical class NNCC(O)=O RRBZUCWNYQUCTR-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical class CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 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 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical class OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 208000007976 Ketosis Diseases 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical class C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical class O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 150000001323 aldoses Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 238000007700 distillative separation Methods 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- WZXYXXWJPMLRGG-UHFFFAOYSA-N hexadecyl benzenesulfonate Chemical class CCCCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 WZXYXXWJPMLRGG-UHFFFAOYSA-N 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 150000002584 ketoses Chemical class 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229940068965 polysorbates Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- OQNGNXKLDCKIIH-UHFFFAOYSA-N tetradecyl benzenesulfonate Chemical class CCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 OQNGNXKLDCKIIH-UHFFFAOYSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3776—Heterocyclic compounds, e.g. lactam
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0021—Dye-stain or dye-transfer inhibiting compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
Definitions
- the present invention relates to liquid compositions containing Polydiallyldimethylamonium compounds and anionic surfactants and optionally water. These agents are useful in preventing dye transfer in wash liquors and, in particular, are useful for preparing color liquid detergents.
- Color liquid detergents are an independent product category in the detergent market. They are distinguished from conventional detergents by a special color protection of the laundry. So-called color transfer inhibitors should reduce the transfer of color from one garment to the other.
- Known and common transfer inhibitors are polyvinylpyrrolidone (PVP) and its derivatives, e.g. PVP-N-oxide or PVP-betaines.
- PVP polyvinylpyrrolidone
- PVP-N-oxide or PVP-betaines e.g. PVP-N-oxide or PVP-betaines.
- cationic polymers as color transfer inhibitors but also as dye fixative in detergents and fabric care products is described. This also includes the Polydiallyldimethylamoniumchlorid.
- EP 0 462 806 A2 describes a detergent which contains 0.01 to 50% by weight of a cationic dye-fixing agent and 1 to 50% by weight of a nonionic surfactant.
- the polydiallyldimethylammonium chloride is disclosed as a suitable color-fixing agent.
- WO 03/057815 A1 describes solid granules which contain 1 to 90% by weight of a water-soluble dye fixing agent.
- suitable color fixers are polydiallyldimethylammonium compounds, especially their salts and copolymers.
- Liquid detergent formulations containing polydiallyldimethylammonium chloride have heretofore been free of anionic surfactants.
- a first subject of the present invention therefore relates to liquid compositions comprising a) at least one polydiallyldialkylammonium compound, b) at least one anionic surfactant and c) at least 16% by weight of water.
- component a) Polydiallyldialkylammoniumchlorid is selected. Particular preference is given to those polymers whose molecular weight is in the range from 1000 to 1,000,000, in particular from 1,000 to 100,000, the range from 2,000 to 20,000 being particularly preferred.
- Polydiallyldialkylammonium compounds in the context of the present invention are known and commercially available.
- the alkyl radicals in these polymers may preferably 1 to 18 carbon atoms, preferably 1 to 4 carbon atoms.
- Particularly preferred is the Polydiallyldimethylammoniumchlorid. They are sold, for example, under the trademark Tinofix FRD® or Lupasol®. Such products preferably have Brookfield viscosities of from 200 to 400 mPas.
- the active substance content (AS) is typically up to 30 to 50%.
- copolymers of polydiallyldimethylammonium in particular copolymers with acrylic acid, methacrylic acid, acrylamides or vinylpyrrolidones, can in principle also be used for the purposes of the present technical teaching.
- compositions for the purposes of the present application also contain anionic surfactants.
- anionic surfactants are alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, glycerol ether sulfates, fatty acid ether sulfates, hydroxy mixed ether sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid
- alkyl and / or alkenyl ether sulfates are preferably selected.
- Alkyl and / or alkenyl ether sulfates which come into consideration as component (b), are known and commercially available sulfation products of linear fatty alcohols or partially branched oxo alcohols.
- R is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms
- n is a number from 1 to 10
- X is alkali and / or alkaline earth, ammonium, alkylammonium, alkanolammonium or glucammonium.
- Ether sulfates of the type mentioned are industrially produced by sulfation and subsequent neutralization of the corresponding alcohol polyglycol ether.
- Typical examples are the sulfates based on addition products of 1 to 10 and especially 2 to 5 moles of ethylene oxide with caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, Myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and technical mixtures thereof in the form of the sodium, potassium or magnesium salts.
- a further class of preferred anionic surfactants are the alkylbenzenesulfonates (ABS). These preferably follow the formula R'-Ph-SO 3 X in which R 'is a branched, but preferably linear, alkyl radical having 10 to 18 carbon atoms, Ph is a phenyl radical and X is an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium. Preference is given to using dodecylbenzenesulfonates, tetradecylbenzenesulfonates, hexadecylbenzenesulfonates and technical mixtures thereof in the form of the sodium salts.
- ABS alkylbenzenesulfonates
- soaps preferably sodium and potassium soaps
- the ethanolamine salts are also suitable. In this case, amounts between 1 to 45 wt .-%, preferably 1 to 40 wt .-% and in particular of 30 wt .-%, preferably up to 15 wt .-% are preferred.
- the potassium or more preferably the sodium soaps of C 12 - C 18 fatty acids are used.
- a further preferred aspect relates to the fact that it has proved to be advantageous if component b), ie the anionic surfactant or surfactant mixture, is present in at least 3 to 5 times, preferably 5 times, the excess weight of component a) , Particularly preferred are such agents, the anionic surfactants b) in amounts of 0.5 to 70 wt .-%, preferably 0.5 to 50 wt .-% and in particular in amounts of 1 to 25 wt .-%, based on the agent , contain.
- Agents of the present invention are liquid, ie, pumpable at room temperature (21 ° C). Solid means, ie granules or powders, etc. are not included in the sense of the present technical teaching.
- the liquid agents according to the invention preferably have viscosities (according to Hoppler, measured at 20 ° C) of preferably 15,000 to a maximum of 50,000 mPas, whereby the range from 50 to 5,000 may also be preferred.
- Water as component c) is mandatory in amounts of 16 wt .-%, based on the means included.
- the compositions according to the present technical teaching can also be present in highly diluted form and then contain up to 95% by weight of water. Preferably, however, they contain less water, for example from 20 to 80 wt .-%, preferably from 20 to 60 and in particular from 20 to 40 wt .-% water.
- liquid compositions according to the present invention may contain other surfactants, in which nonionic surfactants and especially nonionic surfactants from the class of alkyl (oligo) glycosides, fatty alcohols and / or the alkoxylated, preferably ethoxylated fatty alcohols are selected as suitable agents.
- Alkyl and alkenyl oligoglycosides are known nonionic surfactants which follow formula (II), R 1 O- [G] p (II) in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10. They can be obtained by the relevant methods of preparative organic chemistry.
- the alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose.
- the preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides.
- alkyl and / or alkenyl oligoglycosides having an average degree of oligomerization p of from 1.1 to 3.0. From an application point of view, those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4 are preferred.
- the alkyl or alkenyl radical R 1 can be derived from primary alcohols with 4 to 11, preferably 8 to 10 carbon atoms derived.
- Typical examples are butanol, caproic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol, and technical mixtures thereof, as obtained, for example, in the hydrogenation of technical fatty acid methyl esters or in the hydrogenation of aldehydes from Roelen's oxosynthesis.
- the alkyl or alkenyl radical R 1 can also be derived from primary alcohols having 12 to 22, preferably 12 to 14 carbon atoms. Typical examples are lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol, and technical mixtures thereof which can be obtained as described above. Alkyl oligoglucosides based on hydrogenated C12 / 14 cocoyl alcohol with a DP of 1 to 3
- Alcohol ethoxylates are referred to as fatty alcohol or oxo alcohol ethoxylates and preferably follow the formula (III), R 2 O (CH 2 CH 2 O) n H (III) in which R 2 is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and n is a number from 1 to 50, the range from 3 to 30 and in particular from 3 to 12 being particularly preferred.
- Typical examples are the adducts of an average of 1 to 50, preferably 5 to 40 and especially 10 to 25 moles of, for example, caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol , Petroselinylalkohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, for example, in the high-pressure hydrogenation of technical methyl esters based on fats and oils or aldehydes from Roelen's oxo synthesis and as a monomer fraction in the dimerization of unsaturated fatty alcohols.
- adducts of 10 to 40 moles of ethylene oxide with technical fatty alcohol
- nonionic surfactants in addition to the substances described above, it is also possible for all other nonionic, anionic, cationic and / or amphoteric agents known to the person skilled in the art to be present.
- Typical examples of nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol ethers, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers, optionally partially oxidized alk (en) yloligoglycosides or glucuronic acid derivatives, fatty acid N-alkylglucamides, protein hydrolysates (especially wheat-based vegetable products).
- Nonionic surfactants contain polyglycol ether chains, these may have a conventional, but preferably a narrow homolog distribution.
- cationic surfactants are quaternary ammonium compounds and ester quats, especially quaternized fatty acid trialkanolamine ester salts.
- Typical examples of amphoteric or zwitterionic surfactants are alkylbetaines, alkylamidobetaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds.
- those agents are used which contain nonionic surfactants in amounts of 1 to 35 wt .-%, preferably 5 to 25 wt .-% and in particular from 5 to 20 wt .-%.
- a further additional component may advantageously be soap, which then advantageously in amounts of 1 to 40 wt .-%, preferably from 10 to 38 wt .-% and in particular from 12 to 38 wt .-% based on the total weight of the liquid agent may be included.
- the means gem. of the above description are free of cationic surfactants and in particular free of cationic fabric softeners.
- agents are selected which contain a surfactant mixture consisting of anionic surfactants (other than soaps), alkyl (oligo) glycosides and fatty alcohol alkoxylates in the preferred weight ratio of 1: 1: 4 to 1: 1: 2. If soap is included, then in a ratio of preferably 4: 1 with respect to the other anionic surfactants also present.
- surfactant mixtures which contain anionic and / or nonionic surfactants in amounts of from 50 to 90% by weight are preferred.
- the agents according to the present invention preferably have a pH in the range from 5.5 to 10 and preferably from 7.5 to 10, wherein the range from 8.0 to 9.5 may be particularly preferred.
- the means known to those skilled in the art ie alkalis or acids, can be used.
- the funds gem. The above description is preferably suitable for the production of liquid detergents.
- the agents described above are preferably suitable for formulating liquid detergents. In this case, the components a) to c) are formulated according to the above description with further ingredients to the finished, aqueous liquid detergents.
- a typical aqueous liquid detergent contains (based on the active substance) preferably 5 to 25 wt .-% of nonionic surfactants, 0.5 to 5 wt .-% of anionic surfactants, 0 to 10 wt .-% of soap, 0.01 to 1 Wt .-% of a Polydiallyldialkylammoniumtress and 0.01 to 2 wt .-% of enzymes and 0.1 to 15 wt .-% of solubilizers or lower alcohols, such as glycerol, propanol or ethanol and other auxiliaries and additives, such as Borax, organic carboxylic acids and / or salts.
- solubilizers or lower alcohols such as glycerol, propanol or ethanol and other auxiliaries and additives, such as Borax, organic carboxylic acids and / or salts.
- these agents then have active substance contents of 10 to 20%. But it is also possible to formulate such agents with higher levels of active substance, with
- a further aspect of the present invention relates to the use of a mixture of a polydiallyldimethylammonium compound to at least one anionic surfactant, wherein the anionic surfactant min.
- the anionic surfactant min.
- 3 to 5-fold excess weight of polydiallyldimethylammonium compound is present as a color transfer inhibitor in detergents and preferably in liquid detergents ,
- Such liquid agents may preferably be used as a concentrate, which may then be diluted with water by a detergent manufacturer to the desired use concentration.
- the compositions contain soap, preferably in amounts of from 0.1 to 38% by weight, in particular from 10 to 38% by weight.
- Such concentrates should preferably still be pumpable at 20 ° C.
- the liquid concentrates may have viscosities of up to 20,000 mPas (Hoppler, 60 ° C.).
- the funds gem. above description preferably contain alkyl or alkenyl ether sulfates as anionic surfactants.
- compounds of the general formula R 1 O- [G] p in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10 is to be selected as alkyl (oligo) glycosides.
- Further preferred agents contain compounds of the general formula R 2 O- (CH 2 H 4 O) n -H, in which R 2 is a saturated, unsaturated, branched or unbranched alkyl radical having 8 to 22 C atoms and n is a number from 1 to 50 means.
- the agents described contain anionic surfactants in at least 5 times the amount of polydiallyldialkylammonium chloride.
- anionic surfactants in the sense of component a) as well as the soaps according to component b) in this context are considered as anionic surfactants.
- Particularly preferred as component c) is polydiallyldimethylammonium chloride.
- Liquid preparations made from the above concentrates may have a non-aqueous content in the range of from 5 to 50, and preferably from 15 to 35, weight percent. In the simplest case, these are aqueous solutions of the mixtures mentioned.
- the concentrates according to the invention as described above may also be anhydrous agents which can then be used as compounds.
- anhydrous in the context of this invention means that the agent preferably contains no free water, not bound as water of crystallization or in a comparable form. In some cases, small amounts of free water are tolerable, especially in amounts of 0.1 up to 5% by weight.
- the agents used in the detergent sector may contain further typical ingredients such as builders, bleaches, bleach activators, solvents, detergency boosters, enzymes, enzyme stabilizers, viscosity regulators, grayness inhibitors, optical brighteners, soil repellants, foam inhibitors, inorganic salts and fragrances and dyes like that.
- Suitable liquid builders are ethylenediaminetetraacetic acid, nitrilotriacetic acid, citric acid and inorganic phosphonic acids, e.g. the neutral reacting sodium salts of 1-hydroxyethane-1,1-diphosphonate, which may be present in amounts of 0.5 to 5, preferably 1 to 2 wt .-%.
- the funds gem. of the above description have a good color transfer inhibiting effect and are simultaneously storage-stable.
- the Applicant assumes, without being bound by theory, that the anionic surfactants together with the Polydiallyldimethylamonium compounds, preferably their chlorides, form a stable complex which is itself suitable to disperse the dye molecules in aqueous solution or in solution to keep. This is supported by the fact that only in a comparatively narrow quantitative ratio between anionic surfactants and the color transfer inhibitors in the context of the present invention, an optimal effect is achieved.
- the detergent solutions 1 and 2 were prediluted to a concentration of 350 g / l. 1 ml of this solution was added to 68 ml of a dye solution (containing 0.0045 g / L Doramin blue 200%). To this dyed wash was added 0.1 ml of a dilute aqueous solution of polydiallyldimethylammonium chloride (0.35 g AS / 100 ml concentration). The test solutions were heated on the magnetic stirrer while stirring at 40 ° C. Subsequently, cotton test specimens of size 6X 2.5 cm (test fabric WFK 10A) were added to each test solution.
- the color of the specimens was previously measured with a Minolta Chromameter CR 200 in L ex mode.
- the specimens remained 1 h at 40 ° C with gentle stirring in the wash.
- the specimens were separated from the wash and rinsed with tap water for 2 min.
- the color of the specimens was measured with the Minolta Chromameter CR 200 in L ex mode. The total color distance was calculated from the respective initial values and the final values of the measurements.
- the cationic surfactant-containing agent 2 was tested, once the polydiallyldimethylammonium chloride was present and once not. For a medium 2 without polydialdimethylammonium chloride, a color difference of 14.8 was measured, with polydiallyldimethylammonium chloride but a color difference of 38.0. This shows that the concomitant use of cationic surfactants leads to a deterioration in color transfer inhibition.
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Abstract
Description
Die vorliegende Erfindung betrifft flüssige Mittel, die Polydiallyldimethylamonium-Verbindungen sowie anionische Tenside und ggf. Wasser enthalten. Diese Mittel eignen sich zur Verhinderung des Farbtransfers in Waschlaugen und insbesondere eignen sie sich zur Herstellung von Color-Flüssigwaschmittel.The present invention relates to liquid compositions containing Polydiallyldimethylamonium compounds and anionic surfactants and optionally water. These agents are useful in preventing dye transfer in wash liquors and, in particular, are useful for preparing color liquid detergents.
Color-Flüssigwaschmittel sind eine eigenständige Produktkategorie im Waschmittelmarkt. Sie zeichnen sich gegenüber herkömmlichen Waschmitteln durch einen besonderen Farbschutz der Wäsche aus. Dabei sollen sogenannte Farbtransferinhibitoren eine Übertragung der Farbe von einem Kleidungsstück auf das andere reduzieren. Bekannte und gebräuchliche Transferinhibitoren sind Polyvinylpyrrolidon (PVP) und deren Derivate, wie z.B. PVP-N-Oxid oder PVP-Betaine. Weiterhin wird eine Vielzahl von kationischen Polymeren als Farbtransferinhibitoren aber auch als Farbfixierer in Wasch- und Textilpflegemitteln beschrieben. Dazu gehört auch das Polydiallyldimethylamoniumchlorid. So beschreibt die EP 0 462 806-A2 ein Waschmittel, welches 0,01 bis 50 Gew.-% eines kationischen farbfixierenden Mittels und 1 bis 50 Gew.-% eines nichtionischen Tensids enthält. Dabei wird das Polydiallyldimethylamoniumchlorid als ein geeignetes farbfixierendes Mittel offenbart. In der WO 03/057815 Al werden feste Granulate beschrieben, die 1 bis 90 Gew.-% eines wasserlöslichen Farbfixierers enthalten. Als geeignete Farbfixierer werden auch Polydiallyldimethylamonium-Verbindungen, insbesondere deren Salze und Copolymere offenbart. Allerdings waren bislang nur feste Mittel bekannt, die Polydiallyldimethylamoniumchlorid in Abmischung mit Aniontensiden enthalten. Flüssige Waschmittelformulierungen, die Polydiallyldimethylamoniumchlorid enthalten, waren bislang frei von Aniontensiden.Color liquid detergents are an independent product category in the detergent market. They are distinguished from conventional detergents by a special color protection of the laundry. So-called color transfer inhibitors should reduce the transfer of color from one garment to the other. Known and common transfer inhibitors are polyvinylpyrrolidone (PVP) and its derivatives, e.g. PVP-N-oxide or PVP-betaines. Furthermore, a variety of cationic polymers as color transfer inhibitors but also as dye fixative in detergents and fabric care products is described. This also includes the Polydiallyldimethylamoniumchlorid. Thus, EP 0 462 806 A2 describes a detergent which contains 0.01 to 50% by weight of a cationic dye-fixing agent and 1 to 50% by weight of a nonionic surfactant. In this case, the polydiallyldimethylammonium chloride is disclosed as a suitable color-fixing agent. WO 03/057815 A1 describes solid granules which contain 1 to 90% by weight of a water-soluble dye fixing agent. Also disclosed as suitable color fixers are polydiallyldimethylammonium compounds, especially their salts and copolymers. However, only solid agents containing polydiallyldimethylammonium chloride in admixture with anionic surfactants have heretofore been known. Liquid detergent formulations containing polydiallyldimethylammonium chloride have heretofore been free of anionic surfactants.
Es wurde nun überraschenderweise gefunden, dass es möglich ist, aniontensidhaltige Flüssigwaschmittel mit Polydiallyldialkylammonium-Verbindungen, vorzugsweise den Chloriden stabil zu formulieren. Ein erster Gegenstand der vorliegenden Erfindung betrifft daher flüssige Mittel, enthaltend a) mind. eine Polydiallyldialkylammonium-Verbindung, b) mind. ein anionisches Tensid und c) mind. 16 Gew.-% Wasser. Vorzugsweise wird als Komponente a) Polydiallyldialkylammoniumchlorid ausgewählt. Dabei sind insbesondere solche Polymere ausgewählt, deren Molekulargewicht im Bereich von 1000 bis 1,000.000 liegt, insbesondere 1000 bis 100000, wobei der Bereich von 2000 bis 20.000 besonders bevorzugt seine kann. Polydiallyldialkylammonium-Verbindungen im Sinne der vorliegenden Erfindung sind bekannt und kommerziell erhältlich. Die Alkylreste in diesen Polymeren können vorzugsweise 1 bis 18 C-Atomen aufweisen, vorzugsweise 1 bis 4 C-Atome. Besonders bevorzugt ist dabei das Polydiallyldimethylammoniumchlorid. Sie werden beispielsweise unter der Marke Tinofix FRD® oder Lupasol® vertrieben. Solche Produkte weisen vorzugsweise Brookfield-Viskositäten von 200 bis 400 mPas auf. Der Aktivsubstanzgehalt (AS) liegt typischerweise bis 30 bis 50 %. Neben den Salzen sind im Sinne der vorliegenden technischen Lehre prinzipiell auch die Copolymere des Polydiallyldimethylammoniums einsetzbar, insbesondere CoPolymere mit Acrylsäure, Methacrylsäure, Acrylamiden oder Vinylpyrrolidonen.It has now surprisingly been found that it is possible to stably formulate anionic surfactant-containing liquid detergents with polydiallyldialkylammonium compounds, preferably the chlorides. A first subject of the present invention therefore relates to liquid compositions comprising a) at least one polydiallyldialkylammonium compound, b) at least one anionic surfactant and c) at least 16% by weight of water. Preferably, as component a) Polydiallyldialkylammoniumchlorid is selected. Particular preference is given to those polymers whose molecular weight is in the range from 1000 to 1,000,000, in particular from 1,000 to 100,000, the range from 2,000 to 20,000 being particularly preferred. Polydiallyldialkylammonium compounds in the context of the present invention are known and commercially available. The alkyl radicals in these polymers may preferably 1 to 18 carbon atoms, preferably 1 to 4 carbon atoms. Particularly preferred is the Polydiallyldimethylammoniumchlorid. They are sold, for example, under the trademark Tinofix FRD® or Lupasol®. Such products preferably have Brookfield viscosities of from 200 to 400 mPas. The active substance content (AS) is typically up to 30 to 50%. In addition to the salts, the copolymers of polydiallyldimethylammonium, in particular copolymers with acrylic acid, methacrylic acid, acrylamides or vinylpyrrolidones, can in principle also be used for the purposes of the present technical teaching.
Neben den Polydiallyldimethylamonium-Verbindungen enthalten die Mittel im Sinne der vorliegenden Anmeldung auch noch anionische Tenside. Typische Beispiele für anionische Tenside sind Alkylbenzolsulfonate, Alkansulfonate, Olefinsulfonate, Alkylethersulfonate, Glycerinethersulfonate, α-Methylestersulfonate, Sulfofettsäuren, Alkylsulfate, Glycerinethersulfate, Fettsäureethersulfate, Hydroxymischethersulfate, Monoglycerid(ether)sulfate, Fettsäureamid-(ether)-sulfate, Mono- und Dialkylsulfosuccinate, Mono- und Dialkylsulfosuccinamate, Sulfotriglyceride, Amidseifen, Ethercarbonsäuren und deren Salze, Fettsäureisethionate, Fettsäuresarcosinate, Fettsäuretauride, N-Acylaminosäuren, wie beispielsweise Acyllactylate, Acyltartrate, Acylglutamate und Acylaspartate, Alkyloligoglucosidsulfate, Proteinfettsäurekondensate (insbesondere pflanzliche Produkte auf Weizenbasis) und Alkyl(ether)phosphate. Sofern die anionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen.In addition to the polydiallyldimethylammonium compounds, the compositions for the purposes of the present application also contain anionic surfactants. Typical examples of anionic surfactants are alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, α-methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, glycerol ether sulfates, fatty acid ether sulfates, hydroxy mixed ether sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, N-acylamino acids such as acyl lactylates, acyl tartrates, acyl glutamates and acylaspartates, alkyl oligoglucoside sulfates, protein fatty acid condensates (especially wheat-based vegetable products) and alkyl (ether) phosphates. If the anionic surfactants contain polyglycol ether chains, these may have a conventional, but preferably a narrow homolog distribution.
Dabei sind vorzugsweise Alkyl- und/oder Alkenylethersulfate ausgewählt. Alkyl- und/oder Alkenylethersulfate, die als Komponente (b) in Betracht kommen, stellen bekannte und großtechnisch erhältliche Sulfatierungsprodukte von linearen Fettalkoholen oder teilweise verzweigten Oxoalkoholen dar. Sie folgen dabei vorzugsweise der Formel (I),
RO(CH2CH2O)nSO3X (I)
in der R für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen, n für Zahlen von 1 bis 10 und X für Alkali und/oder Erdalkali, Ammonium, Alkylammonium, Alkanolammonium oder Glucammonium steht. Ethersulfate der genannten Art werden großtechnisch durch Sulfatierung und anschließende Neutralisation der entsprechenden Alkoholpolyglykolether hergestellt. Typische Beispiele sind die Sulfate auf Basis von Anlagerungsprodukten von 1 bis 10 und insbesondere 2 bis 5 Mol Ethylenoxid an Capronalkohol, Caprylalkohol, 2-Ethylhexylalkohol, Caprinalkohol, Laurylalkohol, Isotridecylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalkohol, Petroselinylalkohol, Linolylalkohol, Linolenylalkohol, Elaeostearylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol und Brassidylalkohol sowie deren technische Mischungen in Form der Natrium-, Kalium- oder Magnesiumsalze.In this case, alkyl and / or alkenyl ether sulfates are preferably selected. Alkyl and / or alkenyl ether sulfates, which come into consideration as component (b), are known and commercially available sulfation products of linear fatty alcohols or partially branched oxo alcohols. They preferably follow the formula (I),
RO (CH 2 CH 2 O) n SO 3 X (I)
in which R is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms, n is a number from 1 to 10 and X is alkali and / or alkaline earth, ammonium, alkylammonium, alkanolammonium or glucammonium. Ether sulfates of the type mentioned are industrially produced by sulfation and subsequent neutralization of the corresponding alcohol polyglycol ether. Typical examples are the sulfates based on addition products of 1 to 10 and especially 2 to 5 moles of ethylene oxide with caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, Myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and technical mixtures thereof in the form of the sodium, potassium or magnesium salts.
Eine weitere Klasse bevorzugt ausgewählter anionischer Tenside stellen die Alkylbenzolsulfonate (ABS) dar. Diese folgen vorzugsweise der Formel R'-Ph-SO3X in der R' für einen verzweigten, vorzugsweise jedoch linearen Alkylrest mit 10 bis 18 Kohlenstoffatomen, Ph für einen Phenylrest und X für ein Alkali- und/oder Erdalkalimetall, Ammonium, Alkylammonium, Alkanolammonium oder Glucammonium steht. Vorzugsweise werden Dodecylbenzolsulfonate, Tetradecylbenzolsulfonate, Hexadecylbenzolsulfonate sowie deren technische Gemische in Form der Natriumsalze eingesetzt.A further class of preferred anionic surfactants are the alkylbenzenesulfonates (ABS). These preferably follow the formula R'-Ph-SO 3 X in which R 'is a branched, but preferably linear, alkyl radical having 10 to 18 carbon atoms, Ph is a phenyl radical and X is an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium. Preference is given to using dodecylbenzenesulfonates, tetradecylbenzenesulfonates, hexadecylbenzenesulfonates and technical mixtures thereof in the form of the sodium salts.
Neben den bevorzugt eingesetzten Alkyl- und/oder Alkenylethersulfaten bzw. ABS können auch zusätzlich oder stattdessen Seifen, vorzugsweise Natrium- und Kaliumseifen als Aniontenside in den erfindungsgemäßen Mitteln enthalten sein. Es sind auch die Ethanolaminsalze geeignet. Dabei sind Mengen zwischen 1 bis 45 Gew.-%, vorzugsweise 1 bis 40 Gew.-% und insbesondere von 30 Gew.-%, vorzugsweise bis 15 Gew.-% bevorzugt. Vorzugsweise werden die Kalium- bzw. besonders bevorzugt die Natriumseifen von C12 - C18-Fettsäuren verwendet.In addition to the preferred alkyl and / or alkenyl ether sulfates or ABS, soaps, preferably sodium and potassium soaps, may additionally or instead be present as anionic surfactants in the compositions according to the invention. The ethanolamine salts are also suitable. In this case, amounts between 1 to 45 wt .-%, preferably 1 to 40 wt .-% and in particular of 30 wt .-%, preferably up to 15 wt .-% are preferred. Preferably, the potassium or more preferably the sodium soaps of C 12 - C 18 fatty acids are used.
Ein weiterer bevorzugter Aspekt betrifft den Umstand, dass es sich als vorteilhaft erwiesen hat, wenn die Komponente b), also das anionische Tensid bzw. Tensidgemisch, in mindestens 3 bis 5-fachen, vorzugsweise des 5-fachen Gewichtsüberschuss zur Komponente a) enthalten ist. Besonders bevorzugt sind solche Mittel, die Aniontenside b) in Mengen von 0,5 bis 70 Gew.-%, vorzugsweise 0,5 bis 50 Gew.-% und insbesondere in Mengen von 1 bis 25 Gew.-%, bezogen auf das Mittel, enthalten.
Ebenfalls bevorzugt sind solche Mittel, welche die Komponente a) in Mengen von 0,05 bis 14 Gew.-%, vorzugsweise 0,01 bis 10 Gew.-% und insbesondere von 0,1 bis 5 Gew.-%, bezogen auf das Mittel, enthalten. Mittel der vorliegenden Erfindung sind flüssig, d.h. bei Raumtemperatur (21 °C) pumpbar. Feste Mittel, also Granulate oder Pulver etc. sind aber im Sinne der vorliegenden technischen Lehre nicht umfasst. Die flüssigen Mittel im Sinne der Erfindung weisen vorzugsweise Viskositäten (nach Höppler, bei 20 °C gemessen) von vorzugsweise 15.000 bis maximal 50.000 mPas auf, wobei auch der Bereich von 50 bis 5000 bevorzugt sein kann.A further preferred aspect relates to the fact that it has proved to be advantageous if component b), ie the anionic surfactant or surfactant mixture, is present in at least 3 to 5 times, preferably 5 times, the excess weight of component a) , Particularly preferred are such agents, the anionic surfactants b) in amounts of 0.5 to 70 wt .-%, preferably 0.5 to 50 wt .-% and in particular in amounts of 1 to 25 wt .-%, based on the agent , contain.
Also preferred are those agents which the component a) in amounts of 0.05 to 14 wt .-%, preferably 0.01 to 10 wt .-% and in particular from 0.1 to 5 wt .-%, based on the Means, included. Agents of the present invention are liquid, ie, pumpable at room temperature (21 ° C). Solid means, ie granules or powders, etc. are not included in the sense of the present technical teaching. The liquid agents according to the invention preferably have viscosities (according to Hoppler, measured at 20 ° C) of preferably 15,000 to a maximum of 50,000 mPas, whereby the range from 50 to 5,000 may also be preferred.
Wasser als Komponente c) ist zwingend in Mengen von 16 Gew.-%, bezogen auf die Mittel, enthalten. Die Mittel gemäß der vorliegenden technischen Lehre können aber auch stark verdünnt vorliegen und dann bis zu 95 Gew.-% Wasser enthalten. Vorzugsweise enthalten sie aber weniger Wasser, beispielweise von 20 bis 80 Gew.-%, vorzugsweise von 20 bis 60 und insbesondere von 20 bis 40 Gew.-% Wasser.Water as component c) is mandatory in amounts of 16 wt .-%, based on the means included. However, the compositions according to the present technical teaching can also be present in highly diluted form and then contain up to 95% by weight of water. Preferably, however, they contain less water, for example from 20 to 80 wt .-%, preferably from 20 to 60 and in particular from 20 to 40 wt .-% water.
Neben den oben beschriebenen Komponenten a), b) und c) können die flüssigen Mittel im Sinne der vorliegenden Erfindung noch weitere Tenside enthalten, wobei hier insbesondere nichtionische Tenside und ganz besonders nichtionische Tenside aus der Klasse der Alkyl(oligo)glycoside, der Fettalkohole und/oder der alkoxylierten, vorzugsweise ethoxylierte Fettalkohole als geeignete Mittel ausgewählt sind.In addition to the above-described components a), b) and c), the liquid compositions according to the present invention may contain other surfactants, in which nonionic surfactants and especially nonionic surfactants from the class of alkyl (oligo) glycosides, fatty alcohols and / or the alkoxylated, preferably ethoxylated fatty alcohols are selected as suitable agents.
Alkyl- und Alkenyloligoglykoside stellen bekannte nichtionische Tenside dar, die der Formel (II) folgen,
R1O-[G]p (II)
in der R1 für einen Alkyl- und/oder Alkenylrest mit 4 bis 22 Kohlenstoffatomen, G für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für Zahlen von 1 bis 10 steht. Sie können nach den einschlägigen Verfahren der präparativen organischen Chemie erhalten werden. Die Alkyl- und/oder Alkenyloligoglykoside können sich von Aldosen bzw. Ketosen mit 5 oder 6 Kohlen-toffatomen, vorzugsweise der Glucose ableiten. Die bevorzugten Alkyl- und/oder Alkenyloligoglykoside sind somit Alkyl- und/oder Alkenyloligoglucoside. Die Indexzahl p in der allgemeinen Formel (II) gibt den Oligomerisierungsgrad (DP), d. h. die Verteilung von Mono- und Oligoglykosiden an und steht für eine Zahl zwischen 1 und 10. Während p in einer gegebenen Verbindung stets ganzzahlig sein muss und hier vor allem die Werte p = 1 bis 6 annehmen kann, ist der Wert p für ein bestimmtes Alkyloligoglykosid eine analytisch ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkyl- und/oder Alkenyloligoglykoside mit einem mittleren Oligomerisierungsgrad p von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkyl- und/oder Alkenyloligoglykoside bevorzugt, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,4 liegt. Der Alkyl- bzw. Alkenylrest R1 kann sich von primären Alkoholen mit 4 bis 11, vorzugsweise 8 bis 10 Kohlenstoffatomen ableiten. Typische Beispiele sind Butanol, Capronalkohol, Caprylalkohol, Caprinalkohol und Undecylalkohol sowie deren technische Mischungen, wie sie beispielsweise bei der Hydrierung von technischen Fettsäuremethylestem oder im Verlauf der Hydrierung von Aldehyden aus der Roelen'schen Oxosynthese erhalten werden. Bevorzugt sind Alkyl(oligo)glucoside der Kettenlänge C8-C10 (DP = 1 bis 3), die als Vorlauf bei der destillativen Auftrennung von technischem C8-C18-Kokosfettalkohol anfallen und mit einem Anteil von weniger als 6 Gew.-% C12-Alkohol verunreinigt sein können sowie Alkyloligoglucoside auf Basis technischer C9/11-Oxoalkohole (DP = 1 bis 3). Der Alkyl- bzw. Alkenylrest R1 kann sich ferner auch von primären Alkoholen mit 12 bis 22, vorzugsweise 12 bis 14 Kohlenstoffatomen ableiten. Typische Beispiele sind Laurylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidyl-alkohol, Petroselinylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol, Brassidylalkohol sowie deren technische Gemische, die wie oben beschrieben erhalten werden können. Bevorzugt sind Alkyloligoglucoside auf Basis von gehärtetem C12/14-Kokosalkohol mit einem DP von 1 bis 3.Alkyl and alkenyl oligoglycosides are known nonionic surfactants which follow formula (II),
R 1 O- [G] p (II)
in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10. They can be obtained by the relevant methods of preparative organic chemistry. The alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose. The preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides. The index number p in the general formula (II) indicates the degree of oligomerization (DP), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10. While p in a given compound must always be an integer, and here especially If p = 1 to 6 can be assumed, the value p for a given alkyloligoglycoside is an analytically determined arithmetic quantity, which usually represents a fractional number. Preference is given to using alkyl and / or alkenyl oligoglycosides having an average degree of oligomerization p of from 1.1 to 3.0. From an application point of view, those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4 are preferred. The alkyl or alkenyl radical R 1 can be derived from primary alcohols with 4 to 11, preferably 8 to 10 carbon atoms derived. Typical examples are butanol, caproic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol, and technical mixtures thereof, as obtained, for example, in the hydrogenation of technical fatty acid methyl esters or in the hydrogenation of aldehydes from Roelen's oxosynthesis. Preference is given to alkyl (oligo) glucosides of the chain length C 8 -C 10 (DP = 1 to 3) which are obtained as a feedstock in the distillative separation of technical C 8 -C 18 coconut fatty alcohol and in a proportion of less than 6% by weight. % C 12 alcohol can be contaminated as well as alkyl oligoglucosides based on technical C 9/11 oxo alcohols (DP = 1 to 3). The alkyl or alkenyl radical R 1 can also be derived from primary alcohols having 12 to 22, preferably 12 to 14 carbon atoms. Typical examples are lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol, and technical mixtures thereof which can be obtained as described above. Alkyl oligoglucosides based on hydrogenated C12 / 14 cocoyl alcohol with a DP of 1 to 3
Alkoholethoxylate werden herstellungsbedingt als Fettalkohol- oder Oxoalkoholethoxylate bezeichnet und folgen vorzugsweise der Formel (III),
R2O(CH2CH2O)nH (III)
in der R2 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen und n für Zahlen von 1 bis 50 steht, wobei der Bereich von 3 bis 30 und insbesondere von 3 bis 12 besonders bevorzugt seien kann. Typische Beispiele sind die Addukte von durchschnittlich 1 bis 50, vorzugsweise 5 bis 40 und insbesondere 10 bis 25 Mol an z.B. Capronalkohol, Caprylalkohol, 2-Ethylhexylalkohol, Caprinalkohol, Laurylalkohol, Isotridecylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalkohol, Petroselinylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol und Brassidylalkohol sowie deren technische Mischungen, die z.B. bei der Hochdruckhydrierung von technischen Methylestern auf Basis von Fetten und Ölen oder Aldehyden aus der Roelen'schen Oxosynthese sowie als Monomerfraktion bei der Dimerisierung von ungesättigten Fettalkoholen anfallen. Bevorzugt sind auch Addukte von 10 bis 40 Mol Ethylenoxid an technische Fettalkohole mit 12 bis 18 Kohlenstoffatomen, wie beispielsweise Kokos-, Palm-, Palmkern- oder Talgfettalkohol.Alcohol ethoxylates are referred to as fatty alcohol or oxo alcohol ethoxylates and preferably follow the formula (III),
R 2 O (CH 2 CH 2 O) n H (III)
in which R 2 is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms and n is a number from 1 to 50, the range from 3 to 30 and in particular from 3 to 12 being particularly preferred. Typical examples are the adducts of an average of 1 to 50, preferably 5 to 40 and especially 10 to 25 moles of, for example, caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol , Petroselinylalkohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, for example, in the high-pressure hydrogenation of technical methyl esters based on fats and oils or aldehydes from Roelen's oxo synthesis and as a monomer fraction in the dimerization of unsaturated fatty alcohols. Also preferred are adducts of 10 to 40 moles of ethylene oxide with technical fatty alcohols having 12 to 18 carbon atoms, such as coconut, palm, palm kernel or tallow fatty alcohol.
Als oberflächenaktive Stoffe können neben den oben beschriebenen Substanzen auch alle weiteren dem Fachmann bekannten nichtionische, anionische, kationische und/oder amphotere enthalten sein. Typische Beispiele für nichtionische Tenside sind Fettalkoholpolyglycolether, Alkylphenolpolyglycolether, Fettsäurepolyglycolester, Fettsäureamidpolyglycolether, Fettaminpolyglycolether, alkoxylierte Triglyceride, Mischether bzw. Mischformale, gegebenenfalls partiell oxidierte Alk(en)yloligoglykoside bzw. Glucoronsäurederivate, Fettsäure-N-alkylglucamide, Proteinhydrolysate (insbesondere pflanzliche Produkte auf Weizenbasis), Polyolfettsäureester, Zuckerester, Sorbitanester, Polysorbate und Aminoxide. Sofern die nichtionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen.As surfactants, in addition to the substances described above, it is also possible for all other nonionic, anionic, cationic and / or amphoteric agents known to the person skilled in the art to be present. Typical examples of nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol ethers, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers, optionally partially oxidized alk (en) yloligoglycosides or glucuronic acid derivatives, fatty acid N-alkylglucamides, protein hydrolysates (especially wheat-based vegetable products). , Polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides. If the nonionic surfactants contain polyglycol ether chains, these may have a conventional, but preferably a narrow homolog distribution.
Typische Beispiele für kationische Tenside sind quartäre Ammoniumverbindungen und Esterquats, insbesondere quaternierte Fettsäuretrialkanolaminestersalze. Typische Beispiele für amphotere bzw. zwitterionische Tenside sind Alkylbetaine, Alkylamidobetaine, Aminopropionate, Aminoglycinate, Imidazoliniumbetaine und Sulfobetaine. Bei den genannten Tensiden handelt es sich ausschließlich um bekannte Verbindungen.Typical examples of cationic surfactants are quaternary ammonium compounds and ester quats, especially quaternized fatty acid trialkanolamine ester salts. Typical examples of amphoteric or zwitterionic surfactants are alkylbetaines, alkylamidobetaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds.
Vorzugsweise werden solche Mittel eingesetzt, die nichtionische Tenside in Mengen von 1 bis 35 Gew.-%, vorzugsweise 5 bis 25 Gew.-% und insbesondere von 5 bis 20 Gew.-% enthalten. Eine weitere zusätzliche Komponente kann vorteilhafterweise Seife sein, wobei diese dann vorteilhafterweise in Mengen von 1 bis 40 Gew.-%, vorzugsweise von 10 bis 38 Gew.-% und insbesondere von 12 bis 38 Gew.-% bezogen auf das Gesamtgewicht der flüssigen Mittel enthalten sein kann. Es kann weiterhin vorteilhaft sein, dass die Mittel gem. der obigen Beschreibung frei von kationischen Tensiden und insbesondere frei von kationischen Textilweichmachem sind.
Mit besonderem Vorteil werden dabei solche Mittel ausgewählt, die ein Tensidgemisch bestehend aus Aniontensiden (andere als Seifen), Alkyl(oligo)glycosiden und Fettalkoholalkoxylaten im bevorzugten Gewichtsverhältnis von 1 : 1 : 4 bis 1 : 1 : 2 enthalten. Wenn Seife enthalten ist, dann in einem Verhältnis von vorzugsweise 4 : 1 in Bezug auf die ebenfalls anwesenden anderen anionischen Tenside. Des weiteren gilt, dass Tensidgemische bevorzugt sind, die Anionen- und/oder Nichtionentensiden in Mengen von insgesamt 50 bis 90 Gew.-% enthalten.Preferably, those agents are used which contain nonionic surfactants in amounts of 1 to 35 wt .-%, preferably 5 to 25 wt .-% and in particular from 5 to 20 wt .-%. A further additional component may advantageously be soap, which then advantageously in amounts of 1 to 40 wt .-%, preferably from 10 to 38 wt .-% and in particular from 12 to 38 wt .-% based on the total weight of the liquid agent may be included. It may also be advantageous that the means gem. of the above description are free of cationic surfactants and in particular free of cationic fabric softeners.
With particular advantage, agents are selected which contain a surfactant mixture consisting of anionic surfactants (other than soaps), alkyl (oligo) glycosides and fatty alcohol alkoxylates in the preferred weight ratio of 1: 1: 4 to 1: 1: 2. If soap is included, then in a ratio of preferably 4: 1 with respect to the other anionic surfactants also present. Furthermore, surfactant mixtures which contain anionic and / or nonionic surfactants in amounts of from 50 to 90% by weight are preferred.
Die Mittel im Sinne der vorliegenden Erfindung weisen vorzugsweise einen pH-Wert im Bereich von 5,5 bis 10 und vorzugsweise von 7,5 bis 10, wobei der Bereich von 8,0 bis 9,5 insbesondere bevorzugt sein kann. Zur Einstellung des pH-Werts können die für den Fachmann dazu bekannten Mittel, also Laugen oder Säuren, verwendet werden. Die Mittel gem. der obigen Beschreibung eigenen sich vorzugsweise zur Herstellung von Flüssigwaschmitteln. Die oben beschriebenen Mittel eignen sich vorzugsweise zur Formulierung von Flüssigwaschmitteln. Dabei werden die Komponente a) bis c) gemäß der obigen Beschreibung mit weiteren Inhaltsstoffen zu den fertigen, wässerigen Flüssigwaschmitteln formuliert. Ein typisches wässeriges Flüssigwaschmittel enthält (bezogen aus Aktivsubstanz) vorzugsweise 5 bis 25 Gew.-% an nichtionischen Tensiden, 0,5 bis 5 Gew.-% an anionischen Tensiden, 0 bis 10 Gew.-% an Seife, 0,01 bis 1 Gew.-% an einer Polydiallyldialkylammoniumverbindung und 0,01 bis 2 Gew.-% an Enzymen sowie 0,1 bis 15 Gew.-% an Lösungsvermittlern bzw. niederen Alkoholen, wie Glycerin, Propanol oder Ethanol und anderen Hilfs- und Zusatzstoffen, wie Borax, organische Carbonsäuren und/oder Salze. Der Rest auf 100 % ist dann Wasser. Vorzugsweise weisen diese Mittel dann Aktivsubstanzgehalten von 10 bis 20 % auf. Es ist aber auch möglich, derartige Mittel mit höheren Anteilen an Aktivsubstanz zu formulieren, wobei 40 bis zu 70 % möglich sind.The agents according to the present invention preferably have a pH in the range from 5.5 to 10 and preferably from 7.5 to 10, wherein the range from 8.0 to 9.5 may be particularly preferred. To adjust the pH, the means known to those skilled in the art, ie alkalis or acids, can be used. The funds gem. The above description is preferably suitable for the production of liquid detergents. The agents described above are preferably suitable for formulating liquid detergents. In this case, the components a) to c) are formulated according to the above description with further ingredients to the finished, aqueous liquid detergents. A typical aqueous liquid detergent contains (based on the active substance) preferably 5 to 25 wt .-% of nonionic surfactants, 0.5 to 5 wt .-% of anionic surfactants, 0 to 10 wt .-% of soap, 0.01 to 1 Wt .-% of a Polydiallyldialkylammoniumverbindung and 0.01 to 2 wt .-% of enzymes and 0.1 to 15 wt .-% of solubilizers or lower alcohols, such as glycerol, propanol or ethanol and other auxiliaries and additives, such as Borax, organic carboxylic acids and / or salts. The rest at 100% is then water. Preferably, these agents then have active substance contents of 10 to 20%. But it is also possible to formulate such agents with higher levels of active substance, with 40 up to 70% are possible.
Ein weiterer Aspekt der vorliegenden Erfindung betrifft die Verwendung einer Mischung aus einer Polydiallyldimethylammonium-Verbindung um mind. einem anionischen Tensid, wobei das anionische Tensid mind. im 3 bis 5-fachen Gewichtsüberschuss zur Polydiallyldimethylammonium-Verbindung vorliegt, als Farbtransferinhibitor in Waschmitteln und vorzugsweise in Flüssigwaschmitteln.A further aspect of the present invention relates to the use of a mixture of a polydiallyldimethylammonium compound to at least one anionic surfactant, wherein the anionic surfactant min. In 3 to 5-fold excess weight of polydiallyldimethylammonium compound is present as a color transfer inhibitor in detergents and preferably in liquid detergents ,
Ein zusätzlicher Gegenstand der vorliegenden Erfindung betrifft ein flüssiges Mittel, enthaltend
- a) 60 bis 88 Gew.-% eines Tensidgemisches, enthaltend mind. zwei Tenside, ausgewählt aus der Gruppe der anionischen Tenside mit Ausnahme der Seifen, ethoxylierten Fettalkoholen und Alkyl(oligo)glycoside, mit der Maßgabe, dass mind. ein anionisches Tensid enthalten sein muss
- b) 0 bis 38 Gew.-% Seife
- c) 0,1 bis 1,5 Gew.-% Polydiallyldialkylamoniumchlorid und
- d) 0 bis 5 Gew.-% Wasser.
- a) 60 to 88 wt .-% of a surfactant mixture containing at least two surfactants selected from the group of anionic surfactants with the exception of soaps, ethoxylated fatty alcohols and alkyl (oligo) glycosides, with the proviso that at least one anionic surfactant have to be
- b) 0 to 38 wt .-% soap
- c) 0.1 to 1.5 wt .-% Polydiallyldialkylamoniumchlorid and
- d) 0 to 5 wt .-% water.
Derartige flüssige Mittel können vorzugsweise als Konzentrat verwendet werden, die von einem Waschmittelhersteller anschließend auf die gewünschte Einsatzkonzentration mit Wasser verdünnt werden können. In einer bevorzugten Ausführungsform enthalten die Mittel Seife, vorzugsweise in mengen von 0,1 bis 38 Gew.-%, insbesondere von 10 bis 38 Gew.-%. Solche Konzentrate sollten vorzugsweise bei 20 °C noch pumpbar sein. Die flüssigen Konzentrate können aber Viskositäten von bis zu 20.000 mPas (Höppler, 60 °C) aufweisen.Such liquid agents may preferably be used as a concentrate, which may then be diluted with water by a detergent manufacturer to the desired use concentration. In a preferred embodiment, the compositions contain soap, preferably in amounts of from 0.1 to 38% by weight, in particular from 10 to 38% by weight. Such concentrates should preferably still be pumpable at 20 ° C. However, the liquid concentrates may have viscosities of up to 20,000 mPas (Hoppler, 60 ° C.).
Die Mittel gem. obiger Beschreibung enthalten vorzugsweise Alkyl- bzw. Alkenylethersulfate als Aniontenside. Des weiteren sind Verbindungen der allgemeinen Formel R1O-[G]p, in der R1 für einen Alkyl- und/oder Alkenylrest mit 4 bis 22 Kohlenstoffatomen, G für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für Zahlen von 1 bis 10 steht, als Alkyl(oligo)glycoside auszuwählen. Weitere bevorzugte Mittel enthalten Verbindungen der allgemeinen Formel R2O-(CH2H4O)n-H, in der R2 für einen gesättigten, ungesättigten, verzweigten oder unverzweigten Alkylrest mit 8 bis 22 C-Atomen steht und n eine Zahl von 1 bis 50 bedeutet. Es kann von Vorteil sein, wenn die beschriebenen Mittel Aniontenside in mind. der 5-fachen Menge an Polydiallyldialkylamoniumchlorid enthalten. Dabei gelten in diesem Zusammenhang als Aniontenside sowohl die Aniontenside im Sinne von Komponente a) als auch der Seifen gemäß Komponente b). Besonders bevorzugt als Komponente c) ist das Polydiallyldimethylammoniumchlorid.The funds gem. above description preferably contain alkyl or alkenyl ether sulfates as anionic surfactants. Furthermore, compounds of the general formula R 1 O- [G] p , in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10 is to be selected as alkyl (oligo) glycosides. Further preferred agents contain compounds of the general formula R 2 O- (CH 2 H 4 O) n -H, in which R 2 is a saturated, unsaturated, branched or unbranched alkyl radical having 8 to 22 C atoms and n is a number from 1 to 50 means. It may be advantageous if the agents described contain anionic surfactants in at least 5 times the amount of polydiallyldialkylammonium chloride. In this context, the anionic surfactants in the sense of component a) as well as the soaps according to component b) in this context are considered as anionic surfactants. Particularly preferred as component c) is polydiallyldimethylammonium chloride.
Flüssigen Zubereitungen, die aus den obigen Konzentraten hergestellt werden, können einen nicht wässrigen Anteil im Bereich von 5 bis 50 und vorzugsweise 15 bis 35 Gew.-% aufweisen. Im einfachsten Fall handelt es sich um wässrige Lösungen der genannten Mischungen. Bei den erfindungemäßen Konzentraten gemäß der obigen Beschreibung kann es sich aber auch um wasserfreie Mittel handeln, die dann als Compounds eingesetzt werden können. Dabei bedeutet "wasserfrei" im Rahmen dieser Erfindung, daß das Mittel vorzugsweise kein freies, nicht als Kristallwasser oder in vergleichbarer Form gebundenes Wasser enthält. In einigen Fällen sind geringe Menge an freiem Wasser tolerierbar, insbesondere in Mengen 0,1 bis zu 5 Gew.-%.Liquid preparations made from the above concentrates may have a non-aqueous content in the range of from 5 to 50, and preferably from 15 to 35, weight percent. In the simplest case, these are aqueous solutions of the mixtures mentioned. However, the concentrates according to the invention as described above may also be anhydrous agents which can then be used as compounds. In this context, "anhydrous" in the context of this invention means that the agent preferably contains no free water, not bound as water of crystallization or in a comparable form. In some cases, small amounts of free water are tolerable, especially in amounts of 0.1 up to 5% by weight.
Die im Detergensbereich, vorzugsweise in Flüssigwaschmitteln eingesetzten Mittel können weitere typische Inhaltsstoffe, wie beispielsweise Builder, Bleichmittel, Bleichaktivatoren, Lösungsmittel, Waschkraftverstärker, Enzyme, Enzymstabilisatoren, Viskositätsregulatoren, Vergrauungsinhibitoren, optische Aufheller, Soil repellants, Schauminhibitoren, anorganische Salze sowie Duft- und Farbstoffe und dergleichen enthalten.The agents used in the detergent sector, preferably in liquid detergents, may contain further typical ingredients such as builders, bleaches, bleach activators, solvents, detergency boosters, enzymes, enzyme stabilizers, viscosity regulators, grayness inhibitors, optical brighteners, soil repellants, foam inhibitors, inorganic salts and fragrances and dyes like that.
Geeignete flüssige Builder sind Ethylendiamintetraessigsäure, Nitrilotriessigsäure, Citronensäure sowie anorganische Phosphonsäuren, wie z.B. die neutral reagierenden Natriumsalze von 1-Hydroxyethan-1,1,-diphosphonat, die in Mengen von 0,5 bis 5, vorzugsweise 1 bis 2 Gew.-% zugegen sein können.Suitable liquid builders are ethylenediaminetetraacetic acid, nitrilotriacetic acid, citric acid and inorganic phosphonic acids, e.g. the neutral reacting sodium salts of 1-hydroxyethane-1,1-diphosphonate, which may be present in amounts of 0.5 to 5, preferably 1 to 2 wt .-%.
Die Mittel gem. der obigen Beschreibung weisen eine gute farbtransferinhibierende Wirkung auf und sind gleichzeitig lagerstabil. Die Anmelderin geht, ohne an diese Theorie gebunden zu sein, davon aus, dass die Anionentenside zusammen mit den Polydiallyldimethylamonium-Verbindungen, vorzugsweise deren Chloriden, einen stabilen Komplex bilden, der selbst geeignet ist, die Farbstoffmoleküle in wässeriger Lösung zu dispergieren bzw. in Lösung zu halten. Dies wird gestützt durch den Umstand, dass nur in einem vergleichsweise engen Mengenverhältnis zwischen Aniontensiden und den Farbtransferinhibitoren im Sinne der vorliegenden Erfindung eine optimale Wirkung erzielt wird.The funds gem. of the above description have a good color transfer inhibiting effect and are simultaneously storage-stable. The Applicant assumes, without being bound by theory, that the anionic surfactants together with the Polydiallyldimethylamonium compounds, preferably their chlorides, form a stable complex which is itself suitable to disperse the dye molecules in aqueous solution or in solution to keep. This is supported by the fact that only in a comparatively narrow quantitative ratio between anionic surfactants and the color transfer inhibitors in the context of the present invention, an optimal effect is achieved.
Es wurden zwei Basis-Rezepturen von Flüssigwaschmitteln gemäß der folgenden Tabelle hergestellt.
Zur Prüfung des Farbtransfers wurden die Waschmittellösungen 1 bzw. 2 auf eine Konzentration von 350g/l vorverdünnt. 1 ml dieser Lösung wurde zu 68 ml einer Farbstofflösung ( enthaltend 0,0045g/ L Doramin blau 200%) gegeben. Dieser gefärbten Waschlauge wurden 0,1 ml einer verdünnten wässrigen Lösung von Polydiallyldimetylammoniumchlorid (der Konzentration 0,35g AS/100ml) zugefügt.
Die Prüflösungen wurden auf dem Magnetrührer unter rühren auf 40 °C erwärmt. Anschließend wurden zu jeder Prüflösung Baumwollprüflinge der Größe 6X 2,5 cm (Prüfgewebe WFK 10A) hinzugefügt. Die Farbe der Prüflinge wurde zuvor mit einem Minolta Chromameter CR 200 im L a b Modus vermessen. Die Prüflinge verblieben 1h bei 40°C unter leichtem Rühren in der Waschlauge. Anschließend wurden die Prüflinge von der Waschlauge getrennt und 2 Min mit Leitungswasser gespült. Nach dem Mangeln wurde die Farbe der Prüflinge mit dem Minolta Chromameter CR 200 im L a b Modus gemessen. Aus den jeweiligen Ausgangswerten und den Endwerten der Messungen wurde der Gesamtfarbabstand berechnet.To check the color transfer, the detergent solutions 1 and 2 were prediluted to a concentration of 350 g / l. 1 ml of this solution was added to 68 ml of a dye solution (containing 0.0045 g / L Doramin blue 200%). To this dyed wash was added 0.1 ml of a dilute aqueous solution of polydiallyldimethylammonium chloride (0.35 g AS / 100 ml concentration).
The test solutions were heated on the magnetic stirrer while stirring at 40 ° C. Subsequently, cotton test specimens of size 6X 2.5 cm (test fabric WFK 10A) were added to each test solution. The color of the specimens was previously measured with a Minolta Chromameter CR 200 in L ex mode. The specimens remained 1 h at 40 ° C with gentle stirring in the wash. Subsequently, the specimens were separated from the wash and rinsed with tap water for 2 min. After the mangling, the color of the specimens was measured with the Minolta Chromameter CR 200 in L ex mode. The total color distance was calculated from the respective initial values and the final values of the measurements.
Die Rezepturen wurden ggf. um anionische Tenside ergänzt. Dabei wurden die unterschiedlichen Volumina jeweils mit vollentsalztem Wasser ausgeglichen, so das in jedem Fall ein Volumen von 70,1 ml Prüflösung vorlag. Die Ergebnisse finden sich in der folgenden Tabelle 2:
Man erkennt, dass der Gesamtfarbabstand mit dem Zusatz von anionischen Tensiden geringer wird, allerdings bei etwa 3 Gew.-% ein Optimum durchlaufen wird.It can be seen that the total color distance becomes smaller with the addition of anionic surfactants, but at about 3 wt .-% is passed through an optimum.
Es wurde auch das kationtensidhaltige Mittel 2 geprüft, wobei einmal das Polydiallydimethylammoniumchlorid vorhanden war und einmal nicht. Für ein Mittel 2 ohne Polydialldimethylammoniumchlorid wurde ein Farbabstand von 14,8, mit Polydiallyldimethylammoniumchlorid aber ein Farbabstand von 38,0 gemessen. Das zeigt, dass die Mitverwendung von kationischen Tensiden zu einer Verschlechterung der Farbtransferinhibierung führt.Also, the cationic surfactant-containing agent 2 was tested, once the polydiallyldimethylammonium chloride was present and once not. For a medium 2 without polydialdimethylammonium chloride, a color difference of 14.8 was measured, with polydiallyldimethylammonium chloride but a color difference of 38.0. This shows that the concomitant use of cationic surfactants leads to a deterioration in color transfer inhibition.
Claims (23)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004048752A DE102004048752A1 (en) | 2004-10-05 | 2004-10-05 | Liquid surfactant mixtures |
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| EP1645619A1 true EP1645619A1 (en) | 2006-04-12 |
| EP1645619B1 EP1645619B1 (en) | 2009-01-21 |
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| EP05020855A Expired - Lifetime EP1645619B1 (en) | 2004-10-05 | 2005-09-24 | Liquid Detergent Compositions |
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| EP (1) | EP1645619B1 (en) |
| AT (1) | ATE421567T1 (en) |
| DE (2) | DE102004048752A1 (en) |
| ES (1) | ES2321522T3 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007013141A1 (en) | 2007-03-15 | 2008-09-18 | Cognis Ip Management Gmbh | Amphoteric polymers as soil release additives in detergents and cleaners |
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| EP2857489A3 (en) * | 2008-08-28 | 2015-04-29 | The Procter and Gamble Company | Process for preparing a fabric care composition |
| US20100050346A1 (en) * | 2008-08-28 | 2010-03-04 | Corona Iii Alessandro | Compositions and methods for providing a benefit |
| US20110236582A1 (en) | 2010-03-29 | 2011-09-29 | Scheuing David R | Polyelectrolyte Complexes |
| US9309435B2 (en) | 2010-03-29 | 2016-04-12 | The Clorox Company | Precursor polyelectrolyte complexes compositions comprising oxidants |
| US9474269B2 (en) * | 2010-03-29 | 2016-10-25 | The Clorox Company | Aqueous compositions comprising associative polyelectrolyte complexes (PEC) |
| ES2565528T3 (en) * | 2011-12-12 | 2016-04-05 | Unilever N.V. | Laundry compositions |
| US8975220B1 (en) * | 2014-08-11 | 2015-03-10 | The Clorox Company | Hypohalite compositions comprising a cationic polymer |
| ES3014058T3 (en) * | 2015-09-11 | 2025-04-16 | Isp Investments Llc | A stable laundry or cleaning composition, process for preparing the same, and method of use |
| WO2017198438A1 (en) | 2016-05-17 | 2017-11-23 | Unilever Plc | Liquid laundry detergent compositions |
| US20180100123A1 (en) * | 2016-10-12 | 2018-04-12 | Mectra Labs, Inc. | Cleaning solution |
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- 2005-09-24 EP EP05020855A patent/EP1645619B1/en not_active Expired - Lifetime
- 2005-09-24 DE DE502005006518T patent/DE502005006518D1/en not_active Expired - Lifetime
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Also Published As
| Publication number | Publication date |
|---|---|
| US7375071B2 (en) | 2008-05-20 |
| DE102004048752A1 (en) | 2006-04-06 |
| ES2321522T3 (en) | 2009-06-08 |
| EP1645619B1 (en) | 2009-01-21 |
| US20060074005A1 (en) | 2006-04-06 |
| ATE421567T1 (en) | 2009-02-15 |
| DE502005006518D1 (en) | 2009-03-12 |
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