WO1990008813A1 - Detergents liquides - Google Patents
Detergents liquides Download PDFInfo
- Publication number
- WO1990008813A1 WO1990008813A1 PCT/EP1990/000115 EP9000115W WO9008813A1 WO 1990008813 A1 WO1990008813 A1 WO 1990008813A1 EP 9000115 W EP9000115 W EP 9000115W WO 9008813 A1 WO9008813 A1 WO 9008813A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- contain
- cleaning agent
- agent according
- anionic
- Prior art date
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- 239000003599 detergent Substances 0.000 title claims abstract description 15
- 239000007788 liquid Substances 0.000 title claims description 11
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000000129 anionic group Chemical group 0.000 claims abstract description 7
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 3
- -1 alkyl ether sulfates Chemical class 0.000 claims description 21
- 239000002904 solvent Substances 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 239000003945 anionic surfactant Substances 0.000 claims description 10
- 239000012459 cleaning agent Substances 0.000 claims description 10
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 9
- 239000002736 nonionic surfactant Substances 0.000 claims description 8
- 239000003792 electrolyte Substances 0.000 claims description 7
- 239000003205 fragrance Substances 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 6
- 238000005260 corrosion Methods 0.000 claims description 5
- 230000007797 corrosion Effects 0.000 claims description 5
- 239000000975 dye Substances 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 3
- 239000002280 amphoteric surfactant Substances 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 3
- 159000000000 sodium salts Chemical class 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 20
- 239000004094 surface-active agent Substances 0.000 abstract description 17
- 238000004851 dishwashing Methods 0.000 abstract description 7
- 150000003839 salts Chemical class 0.000 abstract description 3
- CTTJWXVQRJUJQW-UHFFFAOYSA-N 2,2-dioctyl-3-sulfobutanedioic acid Chemical compound CCCCCCCCC(C(O)=O)(C(C(O)=O)S(O)(=O)=O)CCCCCCCC CTTJWXVQRJUJQW-UHFFFAOYSA-N 0.000 abstract description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 12
- 210000003491 skin Anatomy 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000008961 swelling Effects 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000013543 active substance Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 210000002615 epidermis Anatomy 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 238000001007 flame atomic emission spectroscopy Methods 0.000 description 4
- 239000004872 foam stabilizing agent Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- XYTBCFDEBPQSPG-UHFFFAOYSA-N 2,2-bis(6-methylheptyl)-3-sulfobutanedioic acid Chemical class C(CCCCC(C)C)C(C(C(=O)O)S(=O)(=O)O)(C(=O)O)CCCCCC(C)C XYTBCFDEBPQSPG-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- OXLXSOPFNVKUMU-UHFFFAOYSA-N 1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical class CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC OXLXSOPFNVKUMU-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241001340526 Chrysoclista linneella Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 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
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000004753 textile 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
- 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
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- 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
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
-
- 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
- C11D1/37—Mixtures of compounds all of which are anionic
-
- 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
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- 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
- C11D1/16—Sulfonic acids or sulfuric acid esters; Salts thereof derived from divalent or polyvalent alcohols
-
- 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
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
Definitions
- Liquid washing, rinsing and cleaning agents are usually aqueous solutions of anionic and / or nonionic surfactants and conventional additives. They are used for washing textiles, for cleaning hard surfaces, for example glasses or ceramic materials, plastics, lacquered and polished Surfaces, which can also be metallic in nature, are used. A preferred area of application for such agents is the manual washing of dining utensils and other related equipment. The respective cleaning processes are usually carried out at slightly elevated temperatures. There is always an increased impact on human skin.
- the present invention therefore relates to cleaning agents with strong cleaning performance and improved skin protection.
- the commercially available dishwashing agents which are to be used manually are aqueous solutions of alkyl ether sulfates, that is to say sulfated adducts of ethylene oxide with fatty alcohols, preferably n-alkylbenzenesulfonates and / or alkanesulfonates, optionally also olefin sulfonates or alkyl sulfates, and also nonionic surfactants, solubilizers, colorants and fragrances.
- alkyl ether sulfates that is to say sulfated adducts of ethylene oxide with fatty alcohols, preferably n-alkylbenzenesulfonates and / or alkanesulfonates, optionally also olefin sulfonates or alkyl sulfates, and also nonionic surfactants, solubilizers, colorants and fragrances.
- liquid dishwashing detergents which, in addition to alkyl sulfates or alkyl ether sulfates, contain alkyl sulfosuccinates in the form of dialkyl (C 7 -C 9 ) esters of sulfosuccinic acid.
- the agents can additionally contain other detergents, hydrotropes, solvents, opaque agents, phosphates, silicates, dyes, fragrances and skin-friendly additives.
- EP 71 411 discloses a detergent composition comprising a mixture of di (C 8 alkyl) and di (C 6 alkyl) sulfosuccinate in combination with other anionic and / or nonionic surfactants.
- European patent specification 112 044 describes dishwashing detergents which contain water-soluble salts of a dialkyl ester of sulfosuccinic acid with identical or different, straight-chain or branched-chain C 3 -C 12 -alkyl radicals and special alkyl ether sulfates. According to European patent 112 045, similar agents should also be added to electrolytes containing magnesium ions.
- foaming liquid detergent compositions composed of C 3 to C 12 dialkyl esters of sulfosuccinic acid, alkyl ether sulfates and / or polyethoxylated nonionic detergents and also carboxylic acid di (C 2 -C 3 ) alkanolamides.
- aqueous mixture of alkyl sulfosuccinates and alkyl ether sulfates is also known from European patent 124367. It also describes aqueous solutions of alkyl sulfosuccinates alone and of alkyl sulfosuccinates in a mixture with alkyl benzene sulfonates.
- Many of the commercially available dishwashing detergents contain, as an anionic surfactant component, salts of alkylbenzenesulfonic acid, which have excellent cleaning effects, but because of their petrochemical origin are to be gradually replaced by other, but at least equally effective, surfactants.
- the present invention therefore relates to liquid detergents for the manual washing of dishes based on an aqueous solution of dialkyl sulfosuccinates, optionally together with other anionic and / or nonionic surfactants and other usual constituents such as solvents, solubilizers, corrosion inhibitors, foam stabilizers, preservatives, electrolytes, thickeners , Dyes and fragrances, which is characterized in that they contain surface-active hydroxysulfonates from unsaturated fatty alcohols having 16 to 22 carbon atoms in the alkyl radical.
- hydroxysulfonates used according to the invention correspond to formulas I or II
- hydroxysulfonates are described in detail in the older German patent application P 37 25 030.2. They are obtained, for example, by using an unsaturated fatty alkyl or fatty alkyl polyoxyalkyl ester of the general formula III
- R 2 CO represents an acyl group with 1 to 4 carbon atoms, reacted with sulfur trioxide, the reaction product in an aqueous solution of 1 to 2.5 moles of alkali, alkaline earth or ammonium hydroxide per mole of SO 3 added and the solution hydrolyzed at 90 to 100 ° C for 0.5 to 240 minutes, cyclic Sulfonation products change into open-chain compounds and at the same time the ester protecting group is saponified quantitatively to recover a terminal OH function.
- the end products may also contain compounds as by-products which are formally derived from formulas (I) and (II) in each case by the loss of a molecule of water.
- the alkaline hydrolysis product can, if desired, be bleached in a manner known per se, for example with hydrogen peroxide or sodium hypochlorite and is in any case with the aid of aqueous mineral acids, e.g. B. hydrochloric acid, adjusted to a pH around 7.
- aqueous mineral acids e.g. B. hydrochloric acid
- an unsaturated fatty alcohol is used.
- the group R 2 -CO can be a formyl, acetyl, propionyl or butyryl group; the acetyl group is preferred.
- the group R 1 is preferably an oleyl group or a fatty alkyl radical consisting predominantly of oleyl groups.
- dialkyl sulfosuccinates used are preferably those with the same straight-chain or branched-chain C ⁇ -alkyl radicals, that is to say di-n-octyl or di-iso-octylsulfosuccinates, in the form of their alkali metal salts, in particular their sodium salts.
- the di-n-octyl sulfosuccinates are particularly preferred.
- the cleaning agents according to the invention show a significantly better skin tolerance in the epidermal swelling test compared to those which contain alkyl ether sulfates, as will be shown below.
- Suitable other common constituents of such agents for the purposes of this invention are solvents, solubilizers, electrolytes, thickeners, corrosion inhibitors, preservatives, foam stabilizers, dyes, fragrances, complexing agents, etc.
- anionic and / or nonionic and / or amphoteric surfactants can also be added to the mixture, provided that they do not interfere with the synergistic effect of the detergent mixture according to the invention.
- composition of the aqueous cleaning agent solution according to the invention is as follows:
- a surfactant mixture consisting of 1 to 50, preferably 2 to 25 parts by weight of a hydroxysulfonate and 50 to 99, preferably 75 to 98 parts by weight of a dialkyl sulfosuccinate,
- anionic surfactant 0 to 10, preferably 0 to 5% by weight of a nonionic surfactant
- anionic surfactants that can be used are, in particular, C 10 to C 18 , in particular C 12 to C 16, alkyl ether sulfates with 1 to 5, preferably 2 to 4, moles of ethylene oxide in the molecule, but also n-alkylbenzenesulfonates with 9 to 16, preferably 12, carbon atoms in the alkyl radical, alkanesulfonates with 10 to 20, preferably 12 to 18 carbon atoms in the alkyl radical, olefin sulfonates with 12 to 16, preferably 12 to 14 carbon atoms in the n-alkyl radical and alkyl sulfates with 8 to 18, preferably 8 to 14 carbon atoms in the alkyl radical and other sulfates or Sulfonates.
- formulations free of alkylbenzenesulfonate are of particular interest.
- Surface-active betaines of the formula I can be used as amphoteric surfactants
- R 1 is an alkyl radical with 8 to 20, preferably 10 to 18 carbon atoms, which is optionally interrupted by heteroatoms or heteroatom groups
- R 2 and R 3 are identical or different alkyl radicals with 1 to 3 carbon atoms.
- C 10 -C 18 -Alkyldimethylcarboxymethylbetaine and C 11 -C 17 -Alkylamidopropyldimethylcarboxymethylbetaine are preferred.
- nonionic surfactants include alkyl glycosides, preferably alkyl glucosides, with 8 to 18, preferably 12 to 16 carbon atoms in the alkyl radical and 1 to 10, preferably 1.2 to 4, glycose units in the molecule and addition products from 4 to 20, preferably from 6 to 15 mol of alkylene oxide, preferably ethylene oxide over C 8 -C 12 alkylbenzenes, C 10 -C 20 -, preferably C 12 -C 18 alkanols, C 10 -C 18 -, carboxylic acid alkanolamides, but also the addition products of ethylene oxide with polypropylene glycols have become known under the name Pluronics (R) , and addition products of 1 to 7 moles of ethylene oxide with C 12 -C 18 -alkanols reacted with 1 to 5 moles of propylene oxide are suitable.
- Pluronics (R) Pluronics
- the solvents to be added if necessary are low molecular weight alkanols with 1 to 4 carbon atoms in the molecule, preferably ethanol and isopropanol.
- Alkanolamines, polyols such as ethylene glycol, 1,2-propylene glycol, glycerol and alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical can be used as solubilizers, for example for small amounts of colorants and fragrances.
- Higher molecular weight ethylene glycols with MG 200 to 600 are also suitable as solubilizers.
- C 8 -C 12 preferably C 8 -C 10 fatty alcohol sulfates and unsaturated C 16 -C 22 , preferably C 16 -C 18 fatty acid sulfonates.
- the preferred thickeners include urea or electrolytes such as sodium chloride, ammonium chloride and magnesium chloride, which can also be used in combination.
- the totality of solvents, solubilizers, thickeners and electrolytes, which can be used individually or in any mixtures with one another, is also referred to as a viscosity regulator.
- corrosion inhibitors and preservatives examples include sodium benzoate and sodium sulfite.
- Known fatty acid alkanolamides can be used as foam stabilizers.
- the liquid cleaning agents according to the invention can also contain conventional disinfectants such as bactericides or fungicides, provided that they have no effect on the skin-protecting effect of the surfactant mixture according to the invention.
- liquid cleaning agents according to the invention of the following examples were obtained by stirring the individual components together obtained in any order and allowing the mixture to stand until there are no bubbles.
- Sodium salts were used as anionic surfactants.
- the application concentration of liquid, manually usable dishwashing detergents is generally 0.1 to 0.5, preferably 0.15 to 0.45 g of active substance (AS) per liter of water.
- i-OAS i-oleyl alcohol sulfonate Na salt based on ocenol
- ABS dodecylbenzenesulfonate Na salt
- FAS C 12 -C 14 fatty alcohol sulfate Na salt
- Di-iO di-iso-octylsulfosuccinate Na salt
- Conserlan KD coconut diethanolamide
- Texapon 842 C 8 fatty alcohol sulfate Na salt
- Texapon NSO C 12/14 -2EO sulfate Na salt (FAES)
- the swelling of swine epidermis served as a measure of the skin tolerance of the surfactant mixtures.
- the required epidermis was obtained immediately after young pigs were slaughtered and stored frozen.
- the Q value of the water-treated skin is therefore by definition 0%, negative values indicate swelling-inhibiting properties.
- the swelling factors for anionic surfactants and systems containing anionic surfactants found using this method correlate very well with measurements of skin tolerance in vivo (cf. J. Soc. Cosmet. Chem. Jap. 20 (1986) 17).
- a number of ready-made dishwashing detergents according to the invention are shown in the table below. They are ideal for use in both hard and soft water.
- the ternary blends with FAES are particularly suitable for obtaining clear, cold-stable formulations.
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- Detergent Compositions (AREA)
Abstract
Dans des détergents de lavage manuel de la vaisselle caractérisés par un fort pouvoir de lavage et par une protection améliorée de la peau, composés de dialkylsulfosuccinates, d'agents tensio-actifs anioniques et non ioniques ainsi que d'hydroxysulfonates d'alcools gras insaturés, les hydroxysulfonates utilisés correspondent à des alcools gras insaturés ayant les formules (I) ou (II), ou à leurs sels alcalins, alcalinoterreux et ammonicaux. Dans les formules (I) et (II), y et z sont compris entre 0 et 18; p est égal à 0, 1 ou 2; (y + z + p) est compris entre 4 et 18; x est compris entre 1 et 20 et n est compris entre 2 et 4. Les dialkysulfosuccinates (sels Na) comprennent des résidus identiques de C8-alkyl à chaîne ramifiée ou de préférence linéaire, tels que le di-n-octylsulfosuccinate. Ces compositions contiennent en tant qu'agents tensio-actifs anioniques supplémentaires des C10 à C18 alkyléthersulfates, de préference des C12 à C16 alkyléthersulfates ayant entre 1 et 5 moles d'éthylènoxyde.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3902619.1 | 1989-01-30 | ||
DE19893902619 DE3902619A1 (de) | 1989-01-30 | 1989-01-30 | Fluessige reinigungsmittel |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1990008813A1 true WO1990008813A1 (fr) | 1990-08-09 |
Family
ID=6373028
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1990/000115 WO1990008813A1 (fr) | 1989-01-30 | 1990-01-22 | Detergents liquides |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0383053A1 (fr) |
DE (1) | DE3902619A1 (fr) |
WO (1) | WO1990008813A1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3926345A1 (de) * | 1989-08-09 | 1991-02-14 | Henkel Kgaa | Waessrige aniontensidkonzentrate mit einem gehalt an oelsaeuresulfonaten sowie die verwendung von oelsaeuresulfonaten als viskositaetsregler fuer waessrige aniontensidkonzentrate |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0112044A1 (fr) * | 1982-11-16 | 1984-06-27 | Unilever N.V. | Compositions détergentes |
FR2564103A1 (fr) * | 1984-05-11 | 1985-11-15 | Unilever Nv | Compositions detergentes |
-
1989
- 1989-01-30 DE DE19893902619 patent/DE3902619A1/de not_active Withdrawn
-
1990
- 1990-01-22 WO PCT/EP1990/000115 patent/WO1990008813A1/fr unknown
- 1990-01-22 EP EP90101194A patent/EP0383053A1/fr not_active Withdrawn
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0112044A1 (fr) * | 1982-11-16 | 1984-06-27 | Unilever N.V. | Compositions détergentes |
FR2564103A1 (fr) * | 1984-05-11 | 1985-11-15 | Unilever Nv | Compositions detergentes |
Also Published As
Publication number | Publication date |
---|---|
EP0383053A1 (fr) | 1990-08-22 |
DE3902619A1 (de) | 1990-08-02 |
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