WO2010031689A1 - All-purpose cleaner with improved cleaning performance in diluted application - Google Patents

All-purpose cleaner with improved cleaning performance in diluted application Download PDF

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Publication number
WO2010031689A1
WO2010031689A1 PCT/EP2009/061290 EP2009061290W WO2010031689A1 WO 2010031689 A1 WO2010031689 A1 WO 2010031689A1 EP 2009061290 W EP2009061290 W EP 2009061290W WO 2010031689 A1 WO2010031689 A1 WO 2010031689A1
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WO
WIPO (PCT)
Prior art keywords
cleaning
agent according
cleaning agent
acid
sodium
Prior art date
Application number
PCT/EP2009/061290
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German (de)
French (fr)
Inventor
Erik BRÜCKNER
Ryszard Katowicz
Stefan Karsten
Original Assignee
Henkel Ag & Co. Kgaa
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Henkel Ag & Co. Kgaa filed Critical Henkel Ag & Co. Kgaa
Priority to ES09782470.0T priority Critical patent/ES2617319T3/en
Priority to EP09782470.0A priority patent/EP2329003B1/en
Publication of WO2010031689A1 publication Critical patent/WO2010031689A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D2111/14

Definitions

  • This application relates to an aqueous hard surface cleaner containing at least one fatty acid or salt thereof and at least one alkylamidoalkylamine. This is particularly suitable for dilute application and can be used in a process for cleaning hard surfaces.
  • a cleaning agent with a combination of a fatty acid or a fatty acid salt and an alkylamidoalkylamine over previously known LAS-free cleaning agents has a significantly improved cleaning performance, especially against greasy or oily soil.
  • Such an agent is also significantly better biodegradable compared with other previously known detergents.
  • an aqueous cleaning agent for hard surfaces which contains at least one fatty acid or a salt thereof and at least one alkylamidoalkylamine.
  • composition according to the invention is suitable for diluted application and can be used for cleaning hard surfaces.
  • a further subject of this application is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces after dilution.
  • the agent according to the invention can be used in a process for cleaning hard surfaces.
  • a method is suitable in which firstly the cleaning agent according to the invention is diluted with water to a cleaning liquor, then the diluted cleaning agent applied to the surface to be cleaned and then by means of a cloth, a sponge, a leather or other suitable means by wiping on the Surface is spread to finally dry.
  • Yet another subject of this application is therefore a process for cleaning hard surfaces, comprising the steps of a) preparing a cleaning liquor by diluting a cleaning agent according to the invention with water, b) applying the diluted cleaning agent to the surface to be cleaned, c) wiping with a cloth, sponge, leather or other suitable substrate for this purpose to rub the agent over the entire surface, d) allow to dry.
  • fatty acids or fatty alcohols or their derivatives - unless otherwise stated - representative of branched or unbranched carboxylic acids or alcohols or their derivatives having preferably 6 to 22 carbon atoms.
  • the former are particularly preferred for their vegetable base as based on renewable raw materials for environmental reasons, but without limiting the teaching of the invention to them.
  • the oxo alcohols or their derivatives which are obtainable, for example, by the RoELEN's oxo synthesis, can also be used correspondingly.
  • alkaline earth metals are referred to below as counterions for monovalent anions, this means that the alkaline earth metal is present only in half - as sufficient to charge balance - amount of substance as the anion.
  • the indication CAS means that the following sequence of numbers is a name of the Chemical Abstracts Service.
  • the agent according to the invention contains at least one fatty acid or a salt thereof.
  • fatty acids are branched or preferably unbranched, saturated or unsaturated carboxylic acids having preferably 6 to 22, in particular 10 to 22, carbon atoms.
  • Particularly preferred fatty acids are unbranched, saturated or unsaturated fatty acids with an even number of carbon atoms, preferably Ci 2 to Ci 8 , since these are obtained from vegetable oils and thus from renewable raw materials.
  • soaps can be used.
  • Soaps are the water-soluble ammonium, alkaline earth and alkali metal salts (preferably sodium salts or potassium salts) of the saturated and unsaturated higher fatty acids (preferably C10 to C22), preferably present as solid or semi-solid mixtures.
  • Typical examples are the sodium, potassium, magnesium, ammonium and triethanolammonium salts of caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, Linoleic acid, linolenic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures.
  • coconut or palm kernel fatty acids are used in the form of their sodium or potassium salts.
  • composition according to the invention preferably contains the at least one fatty acid or the at least one fatty acid salt in an amount of from 0.1 to 5% by weight, particularly preferably 0.5 to 3% by weight, in particular 0.8 to 2% by weight.
  • the agent according to the invention also contains one or more alkylamidoalkylamines.
  • the alkylamidoalkylamines are amphoteric surfactants and obey formula (I),
  • R 1 is a saturated or unsaturated C 6-22 -alkyl radical, preferably C 8 -i 8 -alkyl radical, in particular a saturated Ci -i O 6 alkyl radical, for example a saturated C 2 _i 4 alkyl radical
  • R 2 is a hydrogen atom H or a CI_ 4 alkyl radical, preferably H
  • i is a number from 1 to 10, preferably 2 to 5, in particular 2 or 3
  • R 3 is a hydrogen atom H or CH 2 COOM (to M su), j is a number from 1 to 4, preferably 1 or 2, in particular 1, k is a number from 0 to 4, preferably 0 or 1,
  • Z is CO, SO 2, OPO (OR 4), or P (O) (OR 4) wherein R 4 is a CI_ 4 alkyl or M (see below), and
  • M is a hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, for example protonated mono-, di- or triethanolamine.
  • Preferred representatives satisfy the formulas Ia to Id,
  • alkylamido alkylamines are the following compounds named according to INCI: coco amphodipropionic Acid, Cocobetainamido amphopropionates, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodi- acetate, Disodium Isostearoamphodipropionate , Disodium Laureth-5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium propionate Oleoamphodi-, Disodium PPG-2-lsodeceth-7
  • the alkylamidoalkylamine is preferably selected from the group consisting of disodium cocoamphodiacetate, disodium lauroamphodiacetate, sodium stearo amphoacetate, sodium cocoamphoacetate, disodium cocoamphodipropionate, disodium stearoamphodiacetate and mixtures thereof and particularly preferably disodium cocoamphodiacetate (sodium cocoamphodiacetate).
  • the agent according to the invention preferably contains alkylamidoalkylamines in amounts of from 0.1 to 10% by weight, preferably from 0.2 to 5% by weight.
  • the agent according to the invention also contains at least one nonionic surfactant.
  • Long-chain alkyl polyglycosides containing 8 to 14 C atoms in the alkyl moiety and 1 to 3 glycoside units, Cs-C-is-alcohol polyglycol ethers, ie ethoxylated and / or propoxylated alcohols are especially nonionic surfactants with 8 to 18 carbon atoms in the alkyl moiety and 2 to 15 ethylene oxide (EO) and / or propylene oxide units (PO), C 8 -C 8 - carboxylic acid polyglycol esters having 2 to 15 EO, for example tallow fatty acid + 6-EO esters and ethoxylated fatty acid amides with 12 to 18 carbon atoms in the fatty acid part and 2 to 8 EO mention.
  • EO ethylene oxide
  • PO propylene oxide units
  • surfactants examples include oleyl-cetyl-alcohol with 5 EO, nonylphenol with 10 EO, lauric acid diethanolamide, Kokosalkyldimethylaminoxid and Kokosalkylpolyglucosid with an average of 1, 4 glucose units. Particularly preferred are C 8 . 10- Alkylpolyglucoside with 1 to 2 glycoside units, C 12 -i 8 amine oxides and C 8 . 18 fatty alcohol polyglycol used in particular 2 to 8 EO.
  • composition according to the invention preferably contains one or more nonionic surfactants in an amount of up to 10% by weight, particularly preferably 0.01 to 5% by weight.
  • composition according to the invention may contain further ingredients usually used in cleaning agents.
  • these are selected from the group comprising other surfactants, solvents, bases, acids, viscosity modifiers, polymers, antibacterial agents, preservatives, solubilizers, complexing agents, enzymes, dyes, fragrances and mixtures.
  • the agent according to the invention may contain, in addition to the ingredients mentioned, further surface-active substances.
  • Suitable surface-active substances for the agents according to the invention are surfactants from the classes of anionic, cationic and amphoteric surfactants.
  • Suitable anionic surfactants are preferably C 8 -C 2 o-alkanesulfonates, C 8 -C 18 -Monoalkylsulfate, Cs-C-is-alkyl polyglycol ether sulfates steinklamono- and di-C are suitable with 2 to 6 ethylene oxide (EO) in the ether moiety and sulfosuccinic 8 -C 18 alkyl esters.
  • EO ethylene oxide
  • C 8 -C 18 - ⁇ -olefinsulfonates sulfonated C 8 -C 18 -fatty acids, C 8 -C 22 -carboxylic acid amide ether sulfates, C 8 -C 18 -alkyl polyglycol ether-carboxylates, C 8 -C 18 -N-acyl taurides, C 8 -C 18 -N sarcosinates and C 8 -C 18 -alkyl isethionates or mixtures thereof.
  • the anionic surfactants are preferably used as sodium salts, but can also be used as other alkali metal or alkaline earth metal salts, for example magnesium salts, and in the form of Ammonium or mono-, di-, tri- or Tetraalkylammoniunnsalzen be contained, in the case of sulfonates also in the form of their corresponding acid.
  • examples of such surfactants are sodium cocoalkyl sulfate, sodium sec-alkanesulfonate having about 15 carbon atoms and sodium dioctylsulfosuccinate.
  • the agent according to the invention is free of linear alkylbenzenesulfonate surfactants (LAS), which have hitherto been used frequently in cleaning agents as anionic surfactants.
  • LAS linear alkylbenzenesulfonate surfactants
  • Suitable amphoteric surfactants are, for example, betaines of the formula (R ") (R '") (R v ) N + CH 2 COO - in which R "is an alkyl radical having 8 to 25, preferably 10 to 21, carbon atoms and optionally interrupted by hetero atoms or heteroatom groups R '"and Ri v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular do-C-is-alkyl-dimethylcarboxymethyl betain and Cn-C ⁇ -Alkylamidopropyl-dimethylcarboxymethylbetain.
  • Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R V ) (R VI ) (R V ") (R VI ") N + X " , in which R v to R TM for four identical or different, in particular two long, and two short-chain, alkyl radicals and X 'are an anion, in particular a halide ion, for example, didecyl-dimethyl-ammonium chloride, alkyl-benzyl-didecyl-ammonium chloride and mixtures thereof.
  • the amount of anionic surfactant in the composition according to the invention is usually not more than 10% by weight, preferably between 0.5 and 7% by weight, in particular between 1 and 6% by weight. If the compositions contain cationic and / or amphoteric surfactants, their concentration in the composition according to the invention is usually not more than 3% by weight, preferably in each case between 0.001 and 2% by weight. It has furthermore proven particularly advantageous if the total surfactant content in the composition according to the invention is not more than 8% by weight.
  • the cleaning agent according to the invention may contain one or more water-soluble organic solvents.
  • Suitable solvents are for example, saturated or unsaturated, preferably saturated, branched or unbranched CI_ 2 o-hydrocarbons, preferably C 2 -i 5 hydrocarbons, with at least one hydroxy group and optionally one or more ether functions COC, ie the carbon atom chain interrupting oxygen atoms.
  • Preferred solvents are C 2 -C 6 -alkylene glycols, optionally ethoxylated on one side with a C 1 -C 6 -alkanol, and poly-C 2 -C 3 -alkylene glycol ethers having on average 1 to 9 identical or different, preferably identical, alkylene glycol groups per molecule as well as Ci_ 6 - alcohols, preferably ethanol, n-propanol or iso-propanol, especially ethanol.
  • Exemplary solvents are the following INCI compounds: Alcohol (ethanol), buteth-3, butoxy diglycol, butoxyethanol, butoxyisopropanol, butoxypropanol, n-butyl alcohol, t-butyl alcohol, butylene glycol, butyloctanol, diethylene glycol, dimethoxy diglycol, dimethyl ether, Dipropylene glycol, ethoxydiglycol, ethoxyethanol, ethyl hexanediol, glycol, hexanediol, 1, 2,6-hexanetriol, hexyl alcohol, hexylene glycol, isobutoxypropanol, isopentyldiol, isopropyl alcohol (isopropanol), 3-methoxybutanol, methoxy diglycol, methoxyethanol, methoxyisopropanol, Methoxy methyl butanol, methoxy PEG-10, methylal,
  • the solvent is preferably selected from the group consisting of methanol, ethanol, propanol, isopropanol, ethylene glycol, butyl glycol, propylene glycol, ethylene glycol propyl ether, propylene glycol butyl ether, propylene glycol propyl ether and mixtures thereof. Most preferably, the solvents are ethanol, isopropanol, propylene glycol butyl ether and / or butyl glycol.
  • composition of the invention contains water-soluble organic solvents, preferably in amounts of up to 20 wt .-%, particularly preferably 0.5 to 15 wt .-%, in particular 1 to 10 wt .-%.
  • INCI chelating agents also called sequestrants, are ingredients that are capable of complexing and inactivating metal ions to prevent their detrimental effects on the stability or appearance of the agents, such as clouding. On the one hand, it is important to complex the incompatible with numerous ingredients calcium and magnesium ions of water hardness. On the other hand, the complexation of the ions of heavy metals such as iron or copper delays the oxidative decomposition of the finished agents. In addition, the complexing agents support the cleaning effect. In a preferred embodiment, the agent according to the invention therefore contains one or more complexing agents.
  • Suitable chelating agents are commercially available under the trade name Trilon ®, for example, by the company BASF.
  • the agent according to the invention preferably contains one or more complexing agents selected from the group comprising methylglycinediacetic acid, nitrilotriacetic acid, hydroxyethylidenediphosphonic acid, ethylenediaminetetraacetic acid, polyamines, anionically modified polyamines and mixtures thereof, where the acids are also to be understood as meaning the corresponding sodium salts.
  • Complexing agents are preferably used in amounts of 0.01 to 5 wt .-%.
  • composition according to the invention may also contain agents for the hydrophilization of surfaces.
  • colloidal silica sols in which the silicon dioxide is present nanoparticulate are suitable for hydrophilization.
  • Colloidal nanoparticulate silica sols for the purposes of this invention are stable dispersions of amorphous particulate silicon dioxide SiO 2 having particle sizes in the range from 1 to 100 nm. The particle sizes are preferably in the range from 3 to 50 nm, more preferably from 4 to 40 nm a silica sol, which is suitable to be used for the purposes of this invention is that available under the trade name Bindzil ® 30/360 from Akzo silica sol having a particle size of 9 nm.
  • silica sols are Bindzil ® 15/500, 30/220, 40/200 (Akzo), Nyacol ® 215, 830, 1430, 2034DI and Nyacol ® DP5820, DP5480, DP5540 etc.
  • the silica sols used may also be surface-modified silica treated with sodium aluminate (alumina-modified silica).
  • hydrophilizing polymers are amphoteric polymers, for example copolymers of acrylic or methacrylic acid and MAPTAC, DADMAC or another polymerisable quaternary ammonium compound.
  • copolymers with AMPS (2-acrylamido-2-methylpropanesulfonic acid).
  • Polyethersiloxanes, ie copolymers of polymethylsiloxanes with ethylene oxide or propylene oxide segments are further suitable polymers.
  • acrylic polymers, maleic acid copolymers and polyurethanes with PEG (polyethylene glycol) units are also usable.
  • Suitable polymers are, for example, under the trade names Mirapol Surf-S 100, 110, 200, 210, 400, 410, A 300, A 400 (Rhodia), Tegopren 5843 (Goldschmidt), Sokalan CP 9 (BASF) or Polyquart Ampho 149 (Cognis ) commercially available.
  • agents according to the invention may contain volatile alkali. As such,
  • Ammonia and / or alkanolamines which may contain up to 9 C-atoms in the molecule used.
  • Alkanolamines are the ethanolamines preferred and of these in turn the monoethanolamine.
  • the content of ammonia and / or alkanolamine is preferably 0.01 to 2 wt .-%; ammonia is particularly preferably used.
  • the cleaning agents according to the invention may also contain small amounts of bases.
  • Preferred bases are selected from the group of alkali and alkaline earth metal hydroxides and carbonates, in particular the alkali metal hydroxides, of which potassium hydroxide and especially sodium hydroxide is particularly preferred.
  • Alkaline agents may additionally contain carboxylic acid in addition to the volatile alkali, wherein the equivalent ratio of amine and / or ammonia to carboxylic acid is preferably between 1: 0.9 and 1: 0.1.
  • carboxylic acids having up to 6 carbon atoms, which may be mono-, di- or polycarboxylic acids.
  • the content of carboxylic acid is preferably between 0.01 and 2.7% by weight, in particular between 0.01 and 0.9% by weight.
  • carboxylic acids examples include acetic acid, glycolic acid, lactic acid, citric acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid, of which preferably acetic acid, citric acid and lactic acid are used.
  • Citric acid is particularly preferably used.
  • Viscosity regulators are particularly preferably used.
  • the agent according to the invention may further contain viscosity regulators.
  • Suitable viscosity regulators are, for example, organic natural thickeners (agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, polyoses, guar flour, locust bean gum, starch, dextrins, gelatin, casein), organic modified natural substances (carboxymethylcellulose and other cellulose ethers, hydroxyethyl - and -propylcellulose and the like, core flour ethers), organic fully synthetic thickeners (polyacrylic and polymethacrylic compounds, vinyl polymers, polycarboxylic acids, polyethers, polyimines, polyamides) and inorganic thickeners (polysilicic acids, clay minerals such as montmorillonites, zeolites, silicas).
  • organic natural thickeners agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins,
  • polyacrylic and polymethacrylic compounds include the high molecular weight homopolymers of acrylic acid crosslinked with a polyalkenyl polyether, in particular an allyl ether of sucrose, pentaerythritol or propylene (INCI name according to the International Dictionary of Cosmetic Ingredients of The Cosmetic, Toiletry, and Fragrance Association (US Pat. CTFA): carbomers), also referred to as carboxyvinyl polymers.
  • polyacrylic acids are obtainable inter alia from Fa. 3V Sigma under the tradename Polygel ® such as Polygel ® DA, and by the company.
  • Carbopol ® such as Carbopol ® 940 (molecular weight about 4,000,000), Carbopol ® 941 (molecular weight approximately 1,250,000) or Carbopol ® 934 (molecular weight approximately 3,000,000).
  • acrylic acid copolymers are included: (i) Copolymers of two or more monomers from the group of acrylic acid, methacrylic acid and their simple, preferably with C- ⁇ - 4 alkanols formed esters (INCI acrylates copolymer), to which about Copolymers of methacrylic acid, butyl acrylate and methyl methacrylate (CAS designation according to Chemical Abstracts Service: 25035-69-2) or of butyl acrylate and methyl methacrylate (CAS 25852-37-3) and the example of the Fa.
  • Rohm & Haas under the trade name Aculyn polymer are available ® and Acusol ®, and from Degussa (Goldschmidt) under the trade name Tego ®, for example the anionic non-associative polymers Aculyn ® 22, Aculyn ® 28, Aculyn ® 33 (crosslinked), Acusol ® 810, Acusol ® 823 and Acusol ® 830 (CAS 25852-37-3); (ii) crosslinked high molecular weight acrylic acid copolymers, such as those crosslinked with an allyl ether of sucrose or pentaerythritol copolymers of C 10 - 30 alkyl acrylates with one or more monomers selected from the group of acrylic acid, methacrylic acid and their simple, preferably with C
  • esters (INCI Acrylates / C 10-30 Alkyl Acrylate Crosspolymer) and which are for example available from the company.
  • Carbopol ® for example hydrophobized Carbopol ® ETD 2623 and Carbopol ® 1382 (INCI Acrylates / C 10-30 alkyl acrylate Crosspolymer) and Carbopol AQUA ® 30 (formerly Carbopol ® EX 473).
  • Further thickeners are the polysaccharides and heteropolysaccharides, in particular the polysaccharide gums, for example gum arabic, agar, alginates, carrageenans and their salts, guar, guar gum, tragacanth, gellan, Ramzan, dextran or xanthan and their derivatives, eg propoxylated guar, as well as their mixtures.
  • polysaccharide gums for example gum arabic, agar, alginates, carrageenans and their salts, guar, guar gum, tragacanth, gellan, Ramzan, dextran or xanthan and their derivatives, eg propoxylated guar, as well as their mixtures.
  • polysaccharide thickeners such as starches or cellulose derivatives
  • starches or cellulose derivatives may alternatively or preferably be used in addition to a polysaccharide gum, for example starches of various origins and starch derivatives, for example hydroxyethyl starch, starch phosphate esters or starch acetates, or carboxymethylcellulose or its sodium salt, methyl, ethyl, hydroxyethyl, Hydroxypropyl, hydroxypropyl methyl or hydroxyethyl methyl cellulose or cellulose acetate.
  • starches of various origins and starch derivatives for example hydroxyethyl starch, starch phosphate esters or starch acetates, or carboxymethylcellulose or its sodium salt, methyl, ethyl, hydroxyethyl, Hydroxypropyl, hydroxypropyl methyl or hydroxyethyl methyl cellulose or cellulose acetate.
  • a particularly preferred polysaccharide thickener is the microbial anionic heteropolysaccharide xanthan gum, which is produced by Xanthomonas campestris and some other species under aerobic conditions with a molecular weight of 2-15x10 6 and for example, by Fa. Kelco under the trade names Keltrol ® and Kelzan ® or available from Rhodia under the trade name Rhodopol ®.
  • phyllosilicates include, for example, available under the trade name Laponite ® magnesium or sodium-magnesium phyllosilicates from Solvay Alkali, in particular the Laponite ® RD or Laponite ® RDS, and the magnesium silicates Süd-Chemie, especially the Optigel ® SH.
  • Laponite ® magnesium or sodium-magnesium phyllosilicates from Solvay Alkali
  • the Laponite ® RD or Laponite ® RDS the magnesium silicates Süd-Chemie, especially the Optigel ® SH.
  • the amount of viscosity regulator is usually up to 0.5 wt .-%, preferably 0.001 to 0.3 wt .-%, in particular 0.01 to 0.2 wt .-%, most preferably 0.01 to 0.15 wt .-%.
  • the agent according to the invention is free from viscosity regulators, since these may also contribute to the undesirable streaking.
  • the agent according to the invention may contain further of the auxiliaries and additives mentioned.
  • the pH of the compositions of the invention can be varied over a wide range, but is preferably a range of 2.5 to 12.
  • For the disinfectant is a neutral or slightly acidic pH, preferably 6 to 7.5, in particular 6 , 5 to 7, preferred.
  • Desinfecting hard surface cleaners preferably have a pH of 7.5 to 10, preferably 8 to 9.5, and skin disinfectants are preferably of a weakly acidic pH of 5.0 to 6.0, preferably 5, 5 set. If thickeners are used in the composition according to the invention, the pH is preferably in the neutral range (pH 6.5 to 7.5).
  • compositions according to the invention are preferably formulated as concentrate to be diluted before use. They can be prepared by mixing directly from their raw materials, then mixing and final standing of the agent to freedom from bubbles.
  • the agents according to the invention are preferably used for cleaning hard surfaces. Hard surfaces in the context of this application are windows, mirrors and other glass surfaces, surfaces made of ceramic, plastic, metal or wood and lacquered wood, which are found in household and commercial, such as bathroom ceramics, kitchen surfaces or floors.
  • the cleaning agent is preferably diluted with water before use.
  • Another subject of the invention is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces after dilution.
  • a further subject of the invention is accordingly a process for cleaning hard surfaces, comprising the steps of a) producing a cleaning liquor by diluting a cleaning agent according to one of claims 1 to 9 with water, b) applying the diluted cleaning agent to the surface to be cleaned, c) Wipe with a cloth, sponge, leather or other suitable substrate for this purpose to spread the agent over the entire surface; d) allow to dry.
  • compositions are exemplary compositions:
  • Detergents E1 to E4 according to the invention have been formulated, the composition of which is given in the table below (quantities in% by weight).
  • the pH is adjusted by adding sodium hydroxide.
  • compositions E1 to E4 according to the invention and the comparison agents V1 to V5 were each subjected to a test of the cleaning performance in dilute aqueous solution (12 g / l) in accordance with the quality standards of the Industrie notion Putz- und Vietnamesestoff eV (IPP).
  • IPP Industrie concept Putz- und Vietnamesestoff eV
  • a white surface treated with test soil aged mixture of oil, kaolin and black pigment
  • a cloth soaked with the product to be tested For this purpose, a multi-track wiper device is used.
  • the cleaning result is determined by means of a remission colorimeter against a white standard.
  • compositions of the invention showed a significant increase in the cleaning performance in comparison to the comparative formulations V3 to V5.
  • V1 showed a comparable cleaning performance, but contains in contrast to the inventive compositions a poorly anaerobically degradable linear alkylbenzenesulfonate (LAS).
  • LAS poorly anaerobically degradable linear alkylbenzenesulfonate

Abstract

An aqueous cleaning agent for hard surfaces which contains at least one fatty acid or a salt thereof and at least one alkylamido alkylamine can be used after dilution for cleaning hard surfaces.  The agent can accordingly be used in a method for cleaning hard surfaces which comprises the steps of preparing a cleaning liquor by diluting the cleaning agent with water, applying the diluted cleaning agent to the surface to be cleaned, wiping with a cloth, a sponge, a leather or some other substrate suitable for this purpose in order to distribute the agent over the entire surface and leaving it to dry.

Description

Allzweckreiniger mit verbesserter Reinigungsleistung bei verdünnter Anwendung All-purpose cleaner with improved cleaning performance in diluted applications
Gegenstand dieser Anmeldung ist ein wässriges Reinigungsmittel für harte Oberflächen, das mindestens eine Fettsäure oder ein Salz derselben sowie mindestens ein Alkylamidoalkylamin enthält. Dieses ist insbesondere zur verdünnten Anwendung geeignet und kann in einem Verfahren zur Reinigung harter Oberflächen eingesetzt werden.This application relates to an aqueous hard surface cleaner containing at least one fatty acid or salt thereof and at least one alkylamidoalkylamine. This is particularly suitable for dilute application and can be used in a process for cleaning hard surfaces.
Allzweckreiniger, die zur verdünnten Anwendung vorgesehen sind, enthielten bislang üblicherweise lineare Alkylbenzolsulfonattenside (LAS). Diese weisen eine hervorragende Reinigungsleistung auf, sind jedoch nur schlecht anaerob abbaubar. Die aus ökologischen Gründen erstrebenswerten LAS- freien Tensidkombinationen führten dagegen bislang zu vergleichsweise schlechten Reinigungsergebnissen. Daher war es wünschenswert, ein LAS-freies Reinigungsmittel zu formulieren, das eine bessere biologische Abbaubarkeit besitzt und gleichzeitig eine gute Reinigungsleistung zeigt.All-purpose cleaners intended for dilute use have traditionally contained linear alkyl benzene sulfonate surfactants (LAS). These have excellent cleaning performance, but are poorly degradable anaerobically. By contrast, the LAS-free surfactant combinations, which are desirable for ecological reasons, have so far led to comparatively poor cleaning results. Therefore, it has been desired to formulate a LAS-free detergent which has better biodegradability while exhibiting good cleaning performance.
Es hat sich nun gezeigt, dass ein Reinigungsmittel mit einer Kombination aus einer Fettsäure oder einem Fettsäuresalz und einem Alkylamidoalkylamin gegenüber bisher bekannten LAS-freien Reinigungsmitteln eine deutlich verbesserte Reinigungsleistung aufweist, insbesondere gegenüber fett- oder ölhaltigem Schmutz. Ein solches Mittel ist auch, verglichen mit anderen bisher bekannten Reinigungsmitteln, deutlich besser biologisch abbaubar.It has now been found that a cleaning agent with a combination of a fatty acid or a fatty acid salt and an alkylamidoalkylamine over previously known LAS-free cleaning agents has a significantly improved cleaning performance, especially against greasy or oily soil. Such an agent is also significantly better biodegradable compared with other previously known detergents.
Gegenstand der vorliegenden Anmeldung ist dementsprechend ein wässriges Reinigungsmittel für harte Oberflächen, welches mindestens eine Fettsäure oder ein Salz derselben sowie mindestens ein Alkylamidoalkylamin enthält.Accordingly, the subject matter of the present application is an aqueous cleaning agent for hard surfaces which contains at least one fatty acid or a salt thereof and at least one alkylamidoalkylamine.
Das erfindungsgemäße Mittel eignet sich zur verdünnten Anwendung und kann zur Reinigung harter Oberflächen verwendet werden. Ein weiterer Gegenstand dieser Anmeldung ist daher die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Reinigung harter Oberflächen nach dem Verdünnen.The composition according to the invention is suitable for diluted application and can be used for cleaning hard surfaces. A further subject of this application is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces after dilution.
Das erfindungsgemäße Mittel kann in einem Verfahren zur Reinigung harter Oberflächen eingesetzt werden. Geeignet ist dabei ein Verfahren, bei dem zunächst das erfindungsgemäße Reinigungsmittel mit Wasser zu einer Reinigungsflotte verdünnt wird, das verdünnte Reinigungsmittel dann auf die zu reinigende Oberfläche aufgetragen und anschließend mittels eines Tuchs, eines Schwamms, eines Leders oder eines anderen geeigneten Hilfsmittels durch Wischen auf der Oberfläche verteilt wird, um schließlich zu trocknen.The agent according to the invention can be used in a process for cleaning hard surfaces. In this case, a method is suitable in which firstly the cleaning agent according to the invention is diluted with water to a cleaning liquor, then the diluted cleaning agent applied to the surface to be cleaned and then by means of a cloth, a sponge, a leather or other suitable means by wiping on the Surface is spread to finally dry.
Noch ein weiterer Gegenstand dieser Anmeldung ist daher ein Verfahren zur Reinigung harter Oberflächen, bestehend aus den Schritten a) Herstellung einer Reinigungsflotte durch Verdünnen eines erfindungsgemäßen Reinigungsmittels mit Wasser, b) Auftragen des verdünnten Reinigungsmittels auf die zu reinigende Oberfläche, c) Wischen mit einem Tuch, einem Schwamm, einem Leder oder einem anderen für diesen Zweck geeigneten Substrat, um das Mittel auf der gesamten Oberfläche zu verreiben, d) Trocknen lassen.Yet another subject of this application is therefore a process for cleaning hard surfaces, comprising the steps of a) preparing a cleaning liquor by diluting a cleaning agent according to the invention with water, b) applying the diluted cleaning agent to the surface to be cleaned, c) wiping with a cloth, sponge, leather or other suitable substrate for this purpose to rub the agent over the entire surface, d) allow to dry.
Im Rahmen der vorliegenden Erfindung stehen Fettsäuren bzw. Fettalkohole bzw. deren Derivate - soweit nicht anders angegeben - stellvertretend für verzweigte oder unverzweigte Carbonsäuren bzw. Alkohole bzw. deren Derivate mit vorzugsweise 6 bis 22 Kohlenstoffatomen. Erstere sind insbesondere wegen ihrer pflanzlicher Basis als auf nachwachsenden Rohstoffen basierend aus ökologischen Gründen bevorzugt, ohne jedoch die erfindungsgemäße Lehre auf sie zu beschränken. Insbesondere sind auch die beispielsweise nach der RoELENschen Oxo-Synthese erhältlichen Oxo-Alkohole bzw. deren Derivate entsprechend einsetzbar.In the context of the present invention are fatty acids or fatty alcohols or their derivatives - unless otherwise stated - representative of branched or unbranched carboxylic acids or alcohols or their derivatives having preferably 6 to 22 carbon atoms. The former are particularly preferred for their vegetable base as based on renewable raw materials for environmental reasons, but without limiting the teaching of the invention to them. In particular, the oxo alcohols or their derivatives, which are obtainable, for example, by the RoELEN's oxo synthesis, can also be used correspondingly.
Wann immer im Folgenden Erdalkalimetalle als Gegenionen für einwertige Anionen genannt sind, so bedeutet das, dass das Erdalkalimetall natürlich nur in der halben - zum Ladungsausgleich ausreichenden - Stoffmenge wie das Anion vorliegt.Whenever alkaline earth metals are referred to below as counterions for monovalent anions, this means that the alkaline earth metal is present only in half - as sufficient to charge balance - amount of substance as the anion.
Stoffe, die auch als Inhaltsstoffe von kosmetischen Mitteln dienen, werden nachfolgend ggf. gemäß der International Nomenclature Cosmetic Ingredient (INCI)-Nomenklatur bezeichnet. Chemische Verbindungen tragen eine INCI-Bezeichnung in englischer Sprache, pflanzliche Inhaltsstoffe werden ausschließlich nach Linne in lateinischer Sprache aufgeführt, sogenannte Trivialnamen wie "Wasser", "Honig" oder "Meersalz" werden ebenfalls in lateinischer Sprache angegeben. Die INCI- Bezeichnungen sind dem International Cosmetic Ingredient Dictionary and Handbook - Seventh Edition (1997) zu entnehmen, das von The Cosmetic, Toiletry, and Fragrance Association (CTFA), 1101 17th Street, NW, Suite 300, Washington, DC 20036, USA, herausgegeben wird und mehr als 9.000 INCI- Bezeichnungen sowie Verweise auf mehr als 37.000 Handelsnamen und technische Bezeichnungen einschließlich der zugehörigen Distributoren aus über 31 Ländern enthält. Das International Cosmetic Ingredient Dictionary and Handbook ordnet den Inhaltsstoffen eine oder mehrere chemische Klassen (Chemical Classes), beispielsweise Polymerie Ethers, und eine oder mehrere Funktionen (Functions), beispielsweise Surfactants - Cleansing Agents, zu, die es wiederum näher erläutert und auf die nachfolgend ggf. ebenfalls Bezug genommen wird.Substances which also serve as ingredients of cosmetic products are referred to below, where appropriate, according to the International Nomenclature Cosmetic Ingredient (INCI) nomenclature. Chemical compounds carry an INCI name in English, plant ingredients are listed only after Linne in Latin, so-called trivial names such as "water", "honey" or "sea salt" are also given in Latin. The INCI names can be found in the International Cosmetic Ingredient Dictionary and Handbook - Seventh Edition (1997), The Cosmetic, Toiletry and Fragrance Association (CTFA), 1101 17th Street, NW, Suite 300, Washington, DC 20036, USA , which publishes more than 9,000 INCI names and references to more than 37,000 trade names and technical names, including related distributors from over 31 countries. The International Cosmetic Ingredient Dictionary and Handbook assigns to the ingredients one or more chemical classes, such as polymer ethers, and one or more functions, such as surfactants-cleansing agents, which are further explained and discussed below possibly also referred to.
Die Angabe CAS bedeutet, dass es sich bei der nachfolgenden Zahlenfolge um eine Bezeichnung des Chemical Abstracts Service handelt.The indication CAS means that the following sequence of numbers is a name of the Chemical Abstracts Service.
Fettsäuren und FettsäuresalzeFatty acids and fatty acid salts
Das erfindungsgemäße Mittel enthält mindestens eine Fettsäure oder ein Salz derselben. Fettsäuren im Sinne dieser Anmeldung sind dabei verzweigte oder vorzugsweise unverzweigte, gesättigte oder ungesättigte Carbonsäuren mit vorzugsweise 6 bis 22, insbesondere 10 bis 22 Kohlenstoffatomen. Besonders bevorzugte Fettsäuren sind dabei unverzweigte, gesättigte oder ungesättigte Fettsäuren mit einer geraden Anzahl an Kohlenstoffatomen, vorzugsweise Ci2 bis Ci8, da diese aus pflanzlichen Ölen und somit aus nachwachsenden Rohstoffen gewonnen werden.The agent according to the invention contains at least one fatty acid or a salt thereof. For the purposes of this application, fatty acids are branched or preferably unbranched, saturated or unsaturated carboxylic acids having preferably 6 to 22, in particular 10 to 22, carbon atoms. Particularly preferred fatty acids are unbranched, saturated or unsaturated fatty acids with an even number of carbon atoms, preferably Ci 2 to Ci 8 , since these are obtained from vegetable oils and thus from renewable raw materials.
Neben den Fettsäuren selbst können auch Seifen eingesetzt werden. Als Seifen werden die wasserlöslichen Ammonium-, Erdalkali- und Alkalisalze (vorzugsweise Natriumsalze oder Kaliumsalze) der gesättigten und ungesättigten höheren Fettsäuren (vorzugsweise C10- bis C22-) bezeichnet, die vorzugsweise als feste oder halbfeste Gemische vorliegen. Typische Beispiele sind die Natrium-, Kalium-, Magnesium-, Ammonium- und Triethanolammoniumsalze der Capronsäure, Caprylsäure, 2-Ethyl- hexansäure, Caprinsäure, Laurinsäure, Isotridecansäure, Myristinsäure, Palmitinsäure, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselinsäure, Linolsäure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure sowie deren technische Mischungen. Vorzugsweise werden Kokos- oder Palmkemfettsäure in Form ihrer Natrium- oder Kaliumsalze eingesetzt.In addition to the fatty acids themselves, soaps can be used. Soaps are the water-soluble ammonium, alkaline earth and alkali metal salts (preferably sodium salts or potassium salts) of the saturated and unsaturated higher fatty acids (preferably C10 to C22), preferably present as solid or semi-solid mixtures. Typical examples are the sodium, potassium, magnesium, ammonium and triethanolammonium salts of caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, Linoleic acid, linolenic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures. Preferably, coconut or palm kernel fatty acids are used in the form of their sodium or potassium salts.
Das erfindungsgemäße Mittel enthält die mindestens eine Fettsäure oder das mindestens eine Fettsäuresalz vorzugsweise in einer Menge von 0,1 bis 5 Gew.-%, besonders bevorzugt 0,5 bis 3 Gew.-%, insbesondere 0,8 bis 2 Gew.-%.The composition according to the invention preferably contains the at least one fatty acid or the at least one fatty acid salt in an amount of from 0.1 to 5% by weight, particularly preferably 0.5 to 3% by weight, in particular 0.8 to 2% by weight. ,
Alkylamidoalkylaminealkylamidoalkylamines
Das erfindungsgemäße Mittel enthält weiterhin ein oder mehrere Alkylamidoalkylamine. Die Alkylamidoalkylamine (INCI Alkylamido Alkylamines) sind Amphotenside und gehorchen Formel (I),The agent according to the invention also contains one or more alkylamidoalkylamines. The alkylamidoalkylamines (INCI alkylamido alkylamines) are amphoteric surfactants and obey formula (I),
R1-CO-NR2-(CH2)l-N(R3)-(CH2CH2O)-(CH2)k-[CH(OH)]l-CH2-Z-OM (I)R 1 -CO-NR 2 - (CH 2 ) 1 -N (R 3 ) - (CH 2 CH 2 O) - (CH 2 ) k - [CH (OH)] 1 -CH 2 -Z-OM (I. )
in der R1 ein gesättigter oder ungesättigter C6-22-Alkylrest, vorzugsweise C8-i8-Alkylrest, insbesondere ein gesättigter CiO-i6-Alkylrest, beispielsweise ein gesättigter Ci2_i4-Alkylrest, R2 ein Wasserstoffatom H oder ein Ci_4-Alkylrest, vorzugsweise H, i eine Zahl von 1 bis 10, vorzugsweise 2 bis 5, insbesondere 2 oder 3,in which R 1 is a saturated or unsaturated C 6-22 -alkyl radical, preferably C 8 -i 8 -alkyl radical, in particular a saturated Ci -i O 6 alkyl radical, for example a saturated C 2 _i 4 alkyl radical, R 2 is a hydrogen atom H or a CI_ 4 alkyl radical, preferably H, i is a number from 1 to 10, preferably 2 to 5, in particular 2 or 3,
R3 ein Wasserstoffatom H oder CH2COOM (zu M s.u.), j eine Zahl von 1 bis 4, vorzugsweise 1 oder 2, insbesondere 1 , k eine Zahl von 0 bis 4, vorzugsweise 0 oder 1 ,R 3 is a hydrogen atom H or CH 2 COOM (to M su), j is a number from 1 to 4, preferably 1 or 2, in particular 1, k is a number from 0 to 4, preferably 0 or 1,
I 0 oder 1 , wobei k = 1 ist, wenn I = 1 ist,I 0 or 1, where k = 1, if I = 1,
Z CO, SO2, OPO(OR4) oder P(O)(OR4), wobei R4 ein Ci_4-Alkylrest oder M (s.u.) ist, undZ is CO, SO 2, OPO (OR 4), or P (O) (OR 4) wherein R 4 is a CI_ 4 alkyl or M (see below), and
M ein Wasserstoff, ein Alkalimetall, ein Erdalkalimetall oder ein protoniertes Alkanolamin, z.B. protoniertes Mono-, Di- oder Triethanolamin, ist. Bevorzugte Vertreter genügen den Formeln Ia bis Id,M is a hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, for example protonated mono-, di- or triethanolamine. Preferred representatives satisfy the formulas Ia to Id,
R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2-COOM (Ia)R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 -COOM (Ia)
R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH2-COOM (Ib)R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH 2 -COOM (Ib)
R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH(OH)CH2-SO3M (Ic)R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH (OH) CH 2 -SO 3 M (Ic)
R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH(OH)CH2-OPO3HM (Id)R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH (OH) CH 2 -OPO 3 HM (Id)
in denen R1, R3 und M die gleiche Bedeutung wie in Formel (III) haben.in which R 1 , R 3 and M have the same meaning as in formula (III).
Beispielhafte Alkylamidoalkylamine sind die folgenden gemäß INCI benannten Verbindungen: Coco- amphodipropionic Acid, Cocobetainamido Amphopropionate, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodi- acetate, Disodium Isostearoamphodipropionate, Disodium Laureth-5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium Oleoamphodi- propionate, Disodium PPG-2-lsodeceth-7 Carboxyamphodiacetate, Disodium Stearoamphodiacetate, Disodium Tallowamphodiacetate, Disodium Wheatgermamphodiacetate, Lauroamphodipropionic Acid, Quaternium-85, Sodium Caproamphoacetate, Sodium Caproamphohydroxypropylsulfonate, Sodium Caproamphopropionate, Sodium Capryloamphoacetate, Sodium Capryloamphohydroxypropyl- sulfonate, Sodium Capryloamphopropionate, Sodium Cocoamphoacetate, Sodium Cocoampho- hydroxypropylsulfonate, Sodium Cocoamphopropionate, Sodium Cornamphopropionate, Sodium Iso- stearoamphoacetate, Sodium Isostearoamphopropionate, Sodium Lauroamphoacetate, Sodium Lauro- amphohydroxypropylsulfonate, Sodium Lauroampho PG-Acetate Phosphate, Sodium Lauroampho- propionate, Sodium Myristoamphoacetate, Sodium Oleoamphoacetate, Sodium Oleoamphohydroxy- propylsulfonate, Sodium Oleoamphopropionate, Sodium Ricinoleoamphoacetate, Sodium Stearo- amphoacetate, Sodium Stearoamphohydroxypropylsulfonate, Sodium Stearoamphopropionate, Sodium Tallamphopropionate, Sodium Tallowamphoacetate, Sodium Undecylenoamphoacetate, Sodium Undecylenoamphopropionate, Sodium Wheat Germamphoacetate und Trisodium Lauroampho PG-Acetate Chloride Phosphate. Vorzugsweise ist das Alkylamidoalkylamin ausgewählt aus der Gruppe umfassend Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Sodium Stearo- amphoacetate, Sodium Cocoamphoacetate, Disodium Cocoamphodipropionate, Disodium Stearoamphodiacetate sowie Gemische derselben und insbesondere bevorzugt Disodium Cocoamphodiacetate (Natriumkokosamphodiacetat).Exemplary alkylamido alkylamines are the following compounds named according to INCI: coco amphodipropionic Acid, Cocobetainamido amphopropionates, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodi- acetate, Disodium Isostearoamphodipropionate , Disodium Laureth-5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium propionate Oleoamphodi-, Disodium PPG-2-lsodeceth-7 Carboxyamphodiacetate, Disodium Stearoamphodiacetate, Disodium Tallowamphodiacetate, Disodium Wheatgermamphodiacetate, Lauroamphodipropionic Acid, Quaternium-85, Sodium Caproamphoacetate, Sodium Caproamphohydroxypropylsulfonate, Sodium Caproamphopropionate, Sodium Capryloamphoacetate, Sodium Capryloamphohydroxypropylsulfonate, Sodiu m Capryloamphopropionate, Sodium Cocoamphoacetate, Sodium Cocoampho- hydroxypropylsulfonate, Sodium Cocoamphopropionate, Sodium Cornamphopropionate, Sodium iso stearoamphoacetate, sodium Isostearoamphopropionate, Sodium lauroamphoacetate, sodium Lauro- amphohydroxypropylsulfonate, Sodium Lauroampho PG-Acetate Phosphate, Sodium Lauroampho- propionate, Sodium Myristoamphoacetate, Sodium Oleoamphoacetate , Sodium Oleoamphohydroxy- propylsulfonate, Sodium Oleoamphopropionate, Sodium Ricinoleoamphoacetate, Sodium Stearo- amphoacetates, Sodium Stearoamphohydroxypropylsulfonate, Sodium Stearoamphopropionate, Sodium Tallamphopropionate, Sodium Tallowamphoacetate, Sodium Undecylenoamphoacetate, Sodium Undecylenoamphopropionate, Sodium Wheat Germamphoacetate and Trisodium Lauroampho PG-Acetate Chloride phosphate. The alkylamidoalkylamine is preferably selected from the group consisting of disodium cocoamphodiacetate, disodium lauroamphodiacetate, sodium stearo amphoacetate, sodium cocoamphoacetate, disodium cocoamphodipropionate, disodium stearoamphodiacetate and mixtures thereof and particularly preferably disodium cocoamphodiacetate (sodium cocoamphodiacetate).
Das erfindungsgemäße Mittel enthält Alkylamidoalkylamine vorzugsweise in Mengen von 0,1 bis 10 Gew.-%, vorzugsweise 0,2 bis 5 Gew.-%. Nichtionische TensideThe agent according to the invention preferably contains alkylamidoalkylamines in amounts of from 0.1 to 10% by weight, preferably from 0.2 to 5% by weight. Nonionic surfactants
In einer bevorzugten Ausführungsform enthält das erfindungsgemäße Mittel weiterhin mindestens ein nichtionisches Tensid. Als nichtionische Tenside sind vor allem langkettige Aminoxide mit 12 bis 20 C- Atomen, langkettige Alkylpolyglycoside mit 8 bis 14 C-Atomen im Alkylteil und 1 bis 3 Glycosid- einheiten, Cs-C-is-Alkoholpolyglykolether, d.h. ethoxylierte und/oder propoxylierte Alkohole mit 8 bis 18 C-Atomen im Alkylteil und 2 bis 15 Ethylenoxid- (EO) und/oder Propylenoxideinheiten (PO), C8-Ci8- Carbonsäurepolyglykolester mit 2 bis 15 EO, beispielsweise Talgfettsäure+6-EO-ester und ethoxylierte Fettsäureamide mit 12 bis 18 C-Atomen im Fettsäureteil und 2 bis 8 EO zu erwähnen. Beispiele derartiger Tenside sind Oleyl-Cetyl-Alkohol mit 5 EO, Nonylphenol mit 10 EO, Laurinsäurediethanol- amid, Kokosalkyldimethylaminoxid und Kokosalkylpolyglucosid mit im Mittel 1 ,4 Glucoseeinheiten. Besonders bevorzugt werden C8.10-Alkylpolyglucoside mit 1 bis 2 Glycosideinheiten, C12-i8-Aminoxide sowie C8.18-Fettalkoholpolyglykolether mit insbesondere 2 bis 8 EO eingesetzt.In a preferred embodiment, the agent according to the invention also contains at least one nonionic surfactant. Long-chain alkyl polyglycosides containing 8 to 14 C atoms in the alkyl moiety and 1 to 3 glycoside units, Cs-C-is-alcohol polyglycol ethers, ie ethoxylated and / or propoxylated alcohols, are especially nonionic surfactants with 8 to 18 carbon atoms in the alkyl moiety and 2 to 15 ethylene oxide (EO) and / or propylene oxide units (PO), C 8 -C 8 - carboxylic acid polyglycol esters having 2 to 15 EO, for example tallow fatty acid + 6-EO esters and ethoxylated fatty acid amides with 12 to 18 carbon atoms in the fatty acid part and 2 to 8 EO mention. Examples of such surfactants are oleyl-cetyl-alcohol with 5 EO, nonylphenol with 10 EO, lauric acid diethanolamide, Kokosalkyldimethylaminoxid and Kokosalkylpolyglucosid with an average of 1, 4 glucose units. Particularly preferred are C 8 . 10- Alkylpolyglucoside with 1 to 2 glycoside units, C 12 -i 8 amine oxides and C 8 . 18 fatty alcohol polyglycol used in particular 2 to 8 EO.
Das erfindungsgemäße Mittel enthält ein oder mehrere nichtionische Tenside vorzugsweise in einer Menge von bis zu 10 Gew.-%, besonders bevorzugt 0,01 bis 5 Gew.-%.The composition according to the invention preferably contains one or more nonionic surfactants in an amount of up to 10% by weight, particularly preferably 0.01 to 5% by weight.
Weitere InhaltsstoffeOther ingredients
Neben den genannten kann das erfindungsgemäße Mittel weitere, üblicherweise in Reinigungsmitteln eingesetzte Inhaltsstoffe enthalten. Vorzugsweise sind diese ausgewählt aus der Gruppe umfassend weitere Tenside, Lösungsmittel, Basen, Säuren, Viskositätsveränderer, Polymere, antibakterielle Wirkstoffe, Konservierungsstoffe, Lösungsvermittler, Komplexbildner, Enzyme, Farbstoffe, Duftstoffe sowie Gemische.In addition to those mentioned, the composition according to the invention may contain further ingredients usually used in cleaning agents. Preferably, these are selected from the group comprising other surfactants, solvents, bases, acids, viscosity modifiers, polymers, antibacterial agents, preservatives, solubilizers, complexing agents, enzymes, dyes, fragrances and mixtures.
Tensidesurfactants
Das erfindungsgemäße Mittel kann neben den genannten Inhaltsstoffen weitere oberflächenaktive Substanzen enthalten. Als oberflächenaktive Substanzen eignen sich für die erfindungsgemäßen Mittel Tenside aus den Klassen der anionischen, kationischen und amphoteren Tenside.The agent according to the invention may contain, in addition to the ingredients mentioned, further surface-active substances. Suitable surface-active substances for the agents according to the invention are surfactants from the classes of anionic, cationic and amphoteric surfactants.
Als anionische Tenside eignen sich vorzugsweise C8-C2o-Alkansulfonate, C8-C18-Monoalkylsulfate, Cs-C-is-Alkylpolyglykolethersulfate mit 2 bis 6 Ethylenoxideinheiten (EO) im Etherteil sowie Sulfobern- steinsäuremono- und -di-C8-C18-Alkylester. Weiterhin können auch C8-C18-α-Olefinsulfonate, sulfonierte C8-C18-Fettsäuren, C8-C22-Carbonsäureamidethersulfate, C8-C18-Alkylpolyglykolether- carboxylate, C8-C18-N-Acyltauride, C8-C18-N-Sarkosinate und C8-C18-Alkylisethionate bzw. deren Mischungen verwendet werden.Suitable anionic surfactants are preferably C 8 -C 2 o-alkanesulfonates, C 8 -C 18 -Monoalkylsulfate, Cs-C-is-alkyl polyglycol ether sulfates steinsäuremono- and di-C are suitable with 2 to 6 ethylene oxide (EO) in the ether moiety and sulfosuccinic 8 -C 18 alkyl esters. Furthermore, C 8 -C 18 -α-olefinsulfonates, sulfonated C 8 -C 18 -fatty acids, C 8 -C 22 -carboxylic acid amide ether sulfates, C 8 -C 18 -alkyl polyglycol ether-carboxylates, C 8 -C 18 -N-acyl taurides, C 8 -C 18 -N sarcosinates and C 8 -C 18 -alkyl isethionates or mixtures thereof.
Die anionischen Tenside werden vorzugsweise als Natriumsalze eingesetzt, können aber auch als andere Alkali- oder Erdalkalimetallsalze, beispielsweise Magnesiumsalze, sowie in Form von Ammonium- oder Mono-, Di-, Tri- bzw. Tetraalkylammoniunnsalzen enthalten sein, im Falle der Sulfonate auch in Form ihrer korrespondierenden Säure. Beispiele derartiger Tenside sind Natrium- kokosalkylsulfat, Natrium-sec.-Alkansulfonat mit ca. 15 C-Atomen sowie Natriumdioctylsulfosuccinat. In einer besonders bevorzugten Ausführungsform ist das erfindungsgemäße Mittel dagegen frei von linearen Alkylbenzolsulfonattensiden (LAS), die bislang in Reinigungsmitteln häufig als Aniontenside eingesetzt wurden.The anionic surfactants are preferably used as sodium salts, but can also be used as other alkali metal or alkaline earth metal salts, for example magnesium salts, and in the form of Ammonium or mono-, di-, tri- or Tetraalkylammoniunnsalzen be contained, in the case of sulfonates also in the form of their corresponding acid. Examples of such surfactants are sodium cocoalkyl sulfate, sodium sec-alkanesulfonate having about 15 carbon atoms and sodium dioctylsulfosuccinate. In a particularly preferred embodiment, however, the agent according to the invention is free of linear alkylbenzenesulfonate surfactants (LAS), which have hitherto been used frequently in cleaning agents as anionic surfactants.
Geeignete Amphotenside sind beispielsweise Betaine der Formel (R")(R'")(Riv)N+CH2COO~, in der R" einen gegebenenfalls durch Heteroatome oder Heteroatomgruppen unterbrochenen Alkylrest mit 8 bis 25, vorzugsweise 10 bis 21 Kohlenstoffatomen und R'" sowie Riv gleichartige oder verschiedene Alkyl- reste mit 1 bis 3 Kohlenstoffatomen bedeuten, insbesondere do-C-is-Alkyl-dimethylcarboxymethyl- betain und Cn-C^-Alkylamidopropyl-dimethylcarboxymethylbetain.Suitable amphoteric surfactants are, for example, betaines of the formula (R ") (R '") (R v ) N + CH 2 COO - in which R "is an alkyl radical having 8 to 25, preferably 10 to 21, carbon atoms and optionally interrupted by hetero atoms or heteroatom groups R '"and Ri v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular do-C-is-alkyl-dimethylcarboxymethyl betain and Cn-C ^ -Alkylamidopropyl-dimethylcarboxymethylbetain.
Geeignete Kationtenside sind u.a. die quartären Ammoniumverbindungen der Formel (RV)(RVI)(RV")(RVI")N+ X", in der Rv bis R™ für vier gleich- oder verschiedenartige, insbesondere zwei lang- und zwei kurzkettige, Alkylreste und X' für ein Anion, insbesondere ein Halogenidion, stehen, beispielsweise Didecyl-dimethyl-ammoniumchlorid, Alkyl-benzyl-didecyl-ammoniumchlorid und deren Mischungen.Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R V ) (R VI ) (R V ") (R VI ") N + X " , in which R v to R ™ for four identical or different, in particular two long, and two short-chain, alkyl radicals and X 'are an anion, in particular a halide ion, for example, didecyl-dimethyl-ammonium chloride, alkyl-benzyl-didecyl-ammonium chloride and mixtures thereof.
Die Menge an anionischem Tensid liegt im erfindungsgemäßen Mittel üblicherweise nicht über 10 Gew.-%, vorzugsweise zwischen 0,5 und 7 Gew.-%, insbesondere zwischen 1 und 6 Gew.-%. Sofern die Mittel kationische und/oder amphotere Tenside enthalten, liegt deren Konzentration im erfindungsgemäßen Mittel jeweils üblicherweise nicht über 3 Gew.-%, vorzugsweise jeweils zwischen 0,001 und 2 Gew.-%. Als besonders vorteilhaft hat es sich weiterhin erwiesen, wenn der Tensidgehalt insgesamt im erfindungsgemäßen Mittel nicht mehr als 8 Gew.-% beträgt.The amount of anionic surfactant in the composition according to the invention is usually not more than 10% by weight, preferably between 0.5 and 7% by weight, in particular between 1 and 6% by weight. If the compositions contain cationic and / or amphoteric surfactants, their concentration in the composition according to the invention is usually not more than 3% by weight, preferably in each case between 0.001 and 2% by weight. It has furthermore proven particularly advantageous if the total surfactant content in the composition according to the invention is not more than 8% by weight.
Lösungsmittelsolvent
Als weitere Komponente kann das erfindungsgemäße Reinigungsmittel ein oder mehrere wasserlösliche organische Lösungsmittel enthalten. Geeignete Lösungsmittel sind beispielsweise gesättigte oder ungesättigte, vorzugsweise gesättigte, verzweigte oder unverzweigte Ci_2o-Kohlenwasserstoffe, bevorzugt C2-i5-Kohlenwasserstoffe, mit mindestens einer Hydroxygruppe und gegebenenfalls einer oder mehreren Etherfunktionen C-O-C, d.h. die Kohlenstoffatomkette unterbrechenden Sauerstoffatomen. Bevorzugte Lösungsmittel sind die - gegebenenfalls einseitig mit einem Ci_6-Alkanol ver- etherten - C2-6-Alkylenglykole und Poly-C2-3-alkylenglykolether mit durchschnittlich 1 bis 9 gleichen oder verschiedenen, vorzugsweise gleichen, Alkylenglykolgruppen pro Molekül wie auch die Ci_6- Alkohole, vorzugsweise Ethanol, n-Propanol oder iso-Propanol, insbesondere Ethanol. Beispielhafte Lösungsmittel sind die folgenden gemäß INCI benannten Verbindungen: Alcohol (Ethanol), Buteth-3, Butoxydiglycol, Butoxyethanol, Butoxyisopropanol, Butoxypropanol, n-Butyl Alcohol, t-Butyl Alcohol, Butylene Glycol, Butyloctanol, Diethylene Glycol, Dimethoxydiglycol, Dimethyl Ether, Dipropylene Glycol, Ethoxydiglycol, Ethoxyethanol, Ethyl Hexanediol, Glycol, Hexanediol, 1 ,2,6- Hexanetriol, Hexyl Alcohol, Hexylene Glycol, Isobutoxypropanol, Isopentyldiol, Isopropyl Alcohol (iso-Propanol), 3-Methoxybutanol, Methoxydiglycol, Methoxyethanol, Methoxyisopropanol, Methoxy- methylbutanol, Methoxy PEG-10, Methylal, Methyl Alcohol, Methyl Hexyl Ether, Methylpropanediol, Neopentyl Glycol, PEG-4, PEG-6, PEG-7, PEG-8, PEG-9, PEG-6 Methyl Ether, Pentylene Glycol, PPG-7, PPG-2-Buteth-3, PPG-2 Butyl Ether, PPG-3 Butyl Ether, PPG-2 Methyl Ether, PPG-3 Methyl Ether, PPG-2 Propyl Ether, Propanediol, Propyl Alcohol (n-Propanol), Propylene Glycol, Propylene Glycol Butyl Ether, Propylene Glycol Propyl Ether, Tetrahydrofurfuryl Alcohol, Trimethylhexanol.As a further component, the cleaning agent according to the invention may contain one or more water-soluble organic solvents. Suitable solvents are for example, saturated or unsaturated, preferably saturated, branched or unbranched CI_ 2 o-hydrocarbons, preferably C 2 -i 5 hydrocarbons, with at least one hydroxy group and optionally one or more ether functions COC, ie the carbon atom chain interrupting oxygen atoms. Preferred solvents are C 2 -C 6 -alkylene glycols, optionally ethoxylated on one side with a C 1 -C 6 -alkanol, and poly-C 2 -C 3 -alkylene glycol ethers having on average 1 to 9 identical or different, preferably identical, alkylene glycol groups per molecule as well as Ci_ 6 - alcohols, preferably ethanol, n-propanol or iso-propanol, especially ethanol. Exemplary solvents are the following INCI compounds: Alcohol (ethanol), buteth-3, butoxy diglycol, butoxyethanol, butoxyisopropanol, butoxypropanol, n-butyl alcohol, t-butyl alcohol, butylene glycol, butyloctanol, diethylene glycol, dimethoxy diglycol, dimethyl ether, Dipropylene glycol, ethoxydiglycol, ethoxyethanol, ethyl hexanediol, glycol, hexanediol, 1, 2,6-hexanetriol, hexyl alcohol, hexylene glycol, isobutoxypropanol, isopentyldiol, isopropyl alcohol (isopropanol), 3-methoxybutanol, methoxy diglycol, methoxyethanol, methoxyisopropanol, Methoxy methyl butanol, methoxy PEG-10, methylal, methyl alcohol, methyl hexyl ether, methyl propane diol, neopentyl glycol, PEG-4, PEG-6, PEG-7, PEG-8, PEG-9, PEG-6 methyl ether, pentylenes Glycol, PPG-7, PPG-2-buteth-3, PPG-2 butyl ether, PPG-3 butyl ether, PPG-2 methyl ether, PPG-3 methyl ether, PPG-2 propyl ether, propanediol, propyl alcohol (n Propanol), propylene glycol, propylene glycol butyl ether, propylene glycol colpropyl ether, tetrahydrofurfuryl alcohol, trimethylhexanol.
Vorzugsweise ist das Lösungsmittel ausgewählt aus der Gruppe umfassend Methanol, Ethanol, Propanol, Isopropanol, Ethylenglykol, Butylglykol, Propylenglykol, Ethylenglykolpropylether, Propylen- glykolbutylether, Propylenglykolpropylether sowie Gemischen derselben. Äußerst bevorzugt sind die Lösungsmittel Ethanol, Isopropanol, Propylenglykolbutylether und/oder Butylglykol.The solvent is preferably selected from the group consisting of methanol, ethanol, propanol, isopropanol, ethylene glycol, butyl glycol, propylene glycol, ethylene glycol propyl ether, propylene glycol butyl ether, propylene glycol propyl ether and mixtures thereof. Most preferably, the solvents are ethanol, isopropanol, propylene glycol butyl ether and / or butyl glycol.
Das erfindungsgemäße Mittel enthält wasserlösliche organische Lösungsmittel vorzugsweise in Mengen von bis zu 20 Gew.-%, besonders bevorzugt 0,5 bis 15 Gew.-%, insbesondere 1 bis 10 Gew.-%.The composition of the invention contains water-soluble organic solvents, preferably in amounts of up to 20 wt .-%, particularly preferably 0.5 to 15 wt .-%, in particular 1 to 10 wt .-%.
Komplexbildnercomplexing
Komplexbildner (INCI Chelating Agents), auch Sequestriermittel genannt, sind Inhaltsstoffe, die Metallionen zu komplexieren und inaktivieren vermögen, um ihre nachteiligen Wirkungen auf die Stabilität oder das Aussehen der Mittel, beispielsweise Trübungen, zu verhindern. Einerseits ist es dabei wichtig, die mit zahlreichen Inhaltsstoffen inkompatiblen Calcium- und Magnesiumionen der Wasserhärte zu komplexieren. Die Komplexierung der Ionen von Schwermetallen wie Eisen oder Kupfer verzögert andererseits die oxidative Zersetzung der fertigen Mittel. Zudem unterstützen die Komplexbildner die Reinigungswirkung. In einer bevorzugten Ausführungsform enthält das erfindungsgemäße Mittel daher einen oder mehrere Komplexbildner.INCI chelating agents, also called sequestrants, are ingredients that are capable of complexing and inactivating metal ions to prevent their detrimental effects on the stability or appearance of the agents, such as clouding. On the one hand, it is important to complex the incompatible with numerous ingredients calcium and magnesium ions of water hardness. On the other hand, the complexation of the ions of heavy metals such as iron or copper delays the oxidative decomposition of the finished agents. In addition, the complexing agents support the cleaning effect. In a preferred embodiment, the agent according to the invention therefore contains one or more complexing agents.
Geeignet sind beispielsweise die folgenden, nach Möglichkeit gemäß INCI bezeichneten, Komplexbildner: Aminotrimethylene phosphonic acid, Beta-Alanine Diacetic Acid, Calcium Disodium EDTA, Citric Acid, Cyclodextrin, Cyclohexanediamine Tetraacetic Acid, Diammonium Citrate, Diammonium EDTA, Diethylenetriamine Pentamethylene Phosphonic Acid, Dipotassium EDTA, Disodium Azacyclo- heptane Diphosphonate, Disodium EDTA, Disodium Pyrophosphate, EDTA, Etidronic Acid (HEDP, Hydroxyethylidene diphosphonic acid), Galactaric Acid, Gluconic Acid, Glucuronic Acid, HEDTA, Hydroxypropyl Cyclodextrin, Methyl Cyclodextrin, Pentapotassium Triphosphate, Methyl glycine diacetic acid (MGDA), Pentasodium Aminotrimethylene Phosphonate, Pentasodium Ethylenediamine Tetramethylene Phosphonate, Pentasodium Pentetate, Pentasodium Triphosphate, Pentetic Acid, Phytic Acid, Polyamine, Potassium Citrate, Potassium EDTMP, Potassium Gluconate, Potassium PoIy- phosphate, Potassium Trisphosphonomethylamine Oxide, Ribonic Acid, Sodium Chitosan Methylene Phosphonate, Sodium Citrate, Sodium Diethylenetriamine Pentamethylene Phosphonate, Sodium Dihydroxyethylglycinate, Sodium EDTMP, Sodium Gluceptate, Sodium Gluconate, Sodium Glycereth-1 Polyphosphate, Sodium Hexametaphosphate, Sodium Metaphosphate, Sodium Metasilicate, Sodium Phytate, Sodium Polydimethylglycinophenolsulfonate, Sodium Trimetaphosphate, TEA-EDTA, TEA- Polyphosphate, Tetrahydroxyethyl Ethylenediamine, Tetrahydroxypropyl Ethylenediamine, Tetra- potassium Etidronate, Tetrapotassium Pyrophosphate, Tetrasodium EDTA, Tetrasodium Etidronate, Tetrasodium Pyrophosphate, Tripotassium EDTA, Trisodium Dicarboxymethyl Alaninate, Trisodium EDTA, Trisodium HEDTA, Trisodium MGDA, Trisodium NTA und Trisodium Phosphate. Geeignete Komplexbildner sind beispielsweise von der Firma BASF unter dem Handelsnamen Trilon® kommerziell erhältlich. Bevorzugt enthält das erfindungsgemäße Mittel einen oder mehrere Komplexbildner ausgewählt aus der Gruppe umfassend Methylglycindiessigsäure, Nitrilotriessigsäure, Hydroxy- ethylidendiphosphonsäure, Ethylendiamintetraessigsäure, Polyamine, anionisch modifizierte Polyamine sowie Gemische derselben, wobei unter den Säuren gegebenenfalls auch die korrespondierenden Natriumsalze zu verstehen sind. Komplexbildner werden vorzugsweise in Mengen von 0,01 bis 5 Gew.-% eingesetzt.Suitable, for example, are the following complexing agents, if possible according to INCI: Aminotrimethylene phosphonic acid, Beta-Alanine Diacetic Acid, Calcium Disodium EDTA, Citric Acid, Cyclodextrin, Cyclohexanediamine Tetraacetic Acid, Diammonium Citrate, Diammonium EDTA, Diethylenetriamine Pentamethylene Phosphonic Acid, Dipotassium EDTA , Disodium Azacycloheptane Diphosphonate, Disodium EDTA, Disodium Pyrophosphate, EDTA, Etidronic Acid (HEDP, Hydroxyethylidene diphosphonic Acid), Galactic Acid, Gluconic Acid, Glucuronic Acid, HEDTA, Hydroxypropyl Cyclodextrin, Methyl Cyclodextrin, Pentapotassium Triphosphate, Methyl Glycine Diacetic acid (MGDA), Pentasodium Aminotrimethylene Phosphonates, Pentasodium Ethylenediamine Tetramethylene Phosphonates, Pentasodium Pentetate, Pentasodium Triphosphates, Pentetic Acid, Phytic Acid, Polyamines, Potassium Citrate, Potassium EDTMP, Potassium Gluconate, Potassium Polyphosphates, Potassium Trisphosphonomethylamine Oxides, Ribonic Acid, Sodium Chitosan Methylene Phosphonate, Sodium Citrate, Sodium Diethylenetriamine Pentamethylene Phosphonate, Sodium Dihydroxyethylglycinate, Sodium EDTMP, Sodium Gluceptate, Sodium Gluconate, Sodium Glycereth-1 Polyphosphate, Sodium Hexametaphosphate, Sodium Metaphosphate, Sodium Metasilicate, Sodium Phytate, Sodium Polydimethylglycinophenolsulfonate, Sodium Trimetaphosphate, TEA -EDTA, TEA polyphosphates, tetrahydroxyethyl ethylenediamines, tetrahydroxypropyl ethylenediamines, tetrapotassium etidronates, tetrapotassium pyrophosphates, tetrasodium EDTA, tetrasodium etidronates, tetrasodium pyrophosphates, tripotassium EDTA, trisodium dicarboxymethy Alaninate, Trisodium EDTA, Trisodium HEDTA, Trisodium MGDA, Trisodium NTA and Trisodium Phosphate. Suitable chelating agents are commercially available under the trade name Trilon ®, for example, by the company BASF. The agent according to the invention preferably contains one or more complexing agents selected from the group comprising methylglycinediacetic acid, nitrilotriacetic acid, hydroxyethylidenediphosphonic acid, ethylenediaminetetraacetic acid, polyamines, anionically modified polyamines and mixtures thereof, where the acids are also to be understood as meaning the corresponding sodium salts. Complexing agents are preferably used in amounts of 0.01 to 5 wt .-%.
Hydrophilierende AgenzienHydrophilizing agents
Das erfindungsgemäße Mittel kann auch Mittel zur Hydrophilierung von Oberflächen enthalten. Zur Hydrophilierung eignen sich insbesondere kolloidale Silica-Sole, in denen das Siliciumdioxid vorzugsweise nanopartikulär vorliegt. Kolloidale nanopartikuläre Silica- Sole im Sinne dieser Erfindung sind stabile Dispersionen von amorphem partikulärem Siliciumdioxid SiO2 mit Partikelgrößen im Bereich von 1 bis 100 nm. Vorzugsweise liegen die Teilchengrößen dabei im Bereich 3 bis 50 nm, besonders bevorzugt 4 bis 40 nm. Ein Beispiel für ein Silica- SoI, welches geeignet ist, im Sinne dieser Erfindung eingesetzt zu werden, ist das unter dem Handelsnamen Bindzil® 30/360 von der Firma Akzo erhältliche Silica- SoI mit einer Partikelgröße von 9 nm. Weitere geeignete Silica-Sole sind Bindzil® 15/500, 30/220, 40/200 (Akzo), Nyacol® 215, 830, 1430, 2034DI sowie Nyacol® DP5820, DP5480, DP5540 etc. (Nyacol Products), Levasil® 100/30, 100F/30, 100S/30, 200/30, 200F/30, 300F/30, VP 4038, VP 4055 (H.C. Starck/ Bayer) oder auch CAB-O-SPERSE® PG 001 , PG 002 (wäßrige Dispersionen von CAB-O- SIL®, Cabot), Quartron PL-1 , PL-3 (FusoChemical Co.), Köstrosol 0830, 1030, 1430 (Chemiewerk Bad Köstritz). Bei den eingesetzten Silica-Solen kann es sich auch um oberflächenmodifiziertes Silica handeln, das mit Natriumaluminat behandelt wurde (Alumina-modifiziertes Silica). Daneben lassen sich auch bestimmte Polymere zur Hydrophilierung von Oberflächen einsetzen. Als hydrophilierende Polymere sind insbesondere amphotere Polymer geeignet, beispielsweise Copoly- mere aus Acryl- oder Methacrylsäure und MAPTAC, DADMAC oder einer anderen polymerisierbaren quaternären Ammoniumverbindung. Weiterhin können auch Copolymere mit AMPS (2-Acrylamido-2- methylpropansulfonsäure) verwendet werden. Polyethersiloxane, also Copolymere von Polymethyl- siloxanen mit Ethylenoxid- oder Propylenoxidsegmenten sind weitere geeignete Polymere. Ebenfalls einsetzbar sind Acrylpolymere, Maleinsäure-Copolymere und Polyurethane mit PEG (Polyethylen- glykol) -Einheiten.The composition according to the invention may also contain agents for the hydrophilization of surfaces. In particular, colloidal silica sols in which the silicon dioxide is present nanoparticulate are suitable for hydrophilization. Colloidal nanoparticulate silica sols for the purposes of this invention are stable dispersions of amorphous particulate silicon dioxide SiO 2 having particle sizes in the range from 1 to 100 nm. The particle sizes are preferably in the range from 3 to 50 nm, more preferably from 4 to 40 nm a silica sol, which is suitable to be used for the purposes of this invention is that available under the trade name Bindzil ® 30/360 from Akzo silica sol having a particle size of 9 nm. Further suitable silica sols are Bindzil ® 15/500, 30/220, 40/200 (Akzo), Nyacol ® 215, 830, 1430, 2034DI and Nyacol ® DP5820, DP5480, DP5540 etc. (Nyacol Products), Levasil ® 100/30, 100F / 30, 100S / 30, 200/30, 200F / 30, 300F / 30, VP 4038, VP 4055 (HC Starck / Bayer) or CAB-O-SPERSE ® PG 001, PG 002 (aqueous dispersion of CAB-O-SIL ®, Cabot), Quartron PL-1, PL-3 (Fuso Chemical Co.), Köstrosol 0830, 1030, 1430 (Chemiewerk Bad Köstritz). The silica sols used may also be surface-modified silica treated with sodium aluminate (alumina-modified silica). In addition, it is also possible to use certain polymers for the hydrophilization of surfaces. Particularly suitable hydrophilizing polymers are amphoteric polymers, for example copolymers of acrylic or methacrylic acid and MAPTAC, DADMAC or another polymerisable quaternary ammonium compound. Furthermore, it is also possible to use copolymers with AMPS (2-acrylamido-2-methylpropanesulfonic acid). Polyethersiloxanes, ie copolymers of polymethylsiloxanes with ethylene oxide or propylene oxide segments, are further suitable polymers. Also usable are acrylic polymers, maleic acid copolymers and polyurethanes with PEG (polyethylene glycol) units.
Geeignete Polymere sind beispielsweise unter den Handelsnamen Mirapol Surf-S 100, 110, 200, 210, 400, 410, A 300, A 400 (Rhodia), Tegopren 5843 (Goldschmidt), Sokalan CP 9 (BASF) oder Polyquart Ampho 149 (Cognis) kommerziell erhältlich.Suitable polymers are, for example, under the trade names Mirapol Surf-S 100, 110, 200, 210, 400, 410, A 300, A 400 (Rhodia), Tegopren 5843 (Goldschmidt), Sokalan CP 9 (BASF) or Polyquart Ampho 149 (Cognis ) commercially available.
Flüchtiges Alkali; BasenVolatile alkali; bases
Weiterhin können die erfindungsgemäßen Mittel flüchtiges Alkali enthalten. Als solches werdenFurthermore, the agents according to the invention may contain volatile alkali. As such
Ammoniak und/oder Alkanolamine, die bis zu 9 C-Atome im Molekül enthalten können, verwendet. AlsAmmonia and / or alkanolamines, which may contain up to 9 C-atoms in the molecule used. When
Alkanolamine werden die Ethanolamine bevorzugt und von diesen wiederum das Monoethanolamin.Alkanolamines are the ethanolamines preferred and of these in turn the monoethanolamine.
Der Gehalt an Ammoniak und/oder Alkanolamin beträgt vorzugsweise 0,01 bis 2 Gew.-%; besonders bevorzugt wird Ammoniak eingesetzt.The content of ammonia and / or alkanolamine is preferably 0.01 to 2 wt .-%; ammonia is particularly preferably used.
Daneben können die erfindungsgemäßen Reinigungsmittel auch geringe Mengen an Basen enthalten.In addition, the cleaning agents according to the invention may also contain small amounts of bases.
Bevorzugte Basen stammen aus der Gruppe der Alkali- und Erdalkalimetallhydroxide und -carbonate, insbesondere der Alkalimetallhydroxide, von denen Kaliumhydroxid und vor allem Natriumhydroxid besonders bevorzugt ist.Preferred bases are selected from the group of alkali and alkaline earth metal hydroxides and carbonates, in particular the alkali metal hydroxides, of which potassium hydroxide and especially sodium hydroxide is particularly preferred.
Säurenacids
Alkalische Mittel können neben dem flüchtigen Alkali zusätzlich Carbonsäure enthalten, wobei das Äquivalentverhältnis von Amin und/oder Ammoniak zu Carbonsäure vorzugsweise zwischen 1 : 0,9 und 1 : 0,1 liegt. Geeignet sind Carbonsäuren mit bis zu 6 C-Atomen, wobei es sich um Mono-, Dioder Polycarbonsäuren handeln kann. Je nach Äquivalentgewicht von Amin und Carbonsäure liegt der Gehalt an Carbonsäure vorzugsweise zwischen 0,01 und 2,7 Gew.-%, insbesondere zwischen 0,01 und 0,9 Gew.-%. Beispiele geeigneter Carbonsäuren sind Essigsäure, Glykolsäure, Milchsäure, Citronensäure, Bernsteinsäure, Adipinsäure, Äpfelsäure, Weinsäure und Gluconsäure, von denen vorzugsweise Essigsäure, Citronensäure und Milchsäure verwendet werden. Besonders bevorzugt wird Citronensäure eingesetzt. ViskositätsregulatorenAlkaline agents may additionally contain carboxylic acid in addition to the volatile alkali, wherein the equivalent ratio of amine and / or ammonia to carboxylic acid is preferably between 1: 0.9 and 1: 0.1. Suitable are carboxylic acids having up to 6 carbon atoms, which may be mono-, di- or polycarboxylic acids. Depending on the equivalent weight of amine and carboxylic acid, the content of carboxylic acid is preferably between 0.01 and 2.7% by weight, in particular between 0.01 and 0.9% by weight. Examples of suitable carboxylic acids are acetic acid, glycolic acid, lactic acid, citric acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid, of which preferably acetic acid, citric acid and lactic acid are used. Citric acid is particularly preferably used. Viscosity regulators
Das erfindungsgemäße Mittel kann weiterhin Viskositätsregulatoren enthalten. Geeignete Viskositätsregulatoren sind beispielsweise organische natürliche Verdickungsmittel (Agar-Agar, Carrageen, Tragant, Gummi arabicum, Alginate, Pektine, Polyosen, Guar-Mehl, Johannisbrotbaumkernmehl, Stärke, Dextrine, Gelatine, Casein), organische abgewandelte Naturstoffe (Carboxymethylcellulose und andere Celluloseether, Hydroxyethyl- und -propylcellulose und dergleichen, Kernmehlether), organische vollsynthetische Verdickungsmittel (Polyacryl- und Polymethacryl-Verbindungen, Vinyl- polymere, Polycarbonsäuren, Polyether, Polyimine, Polyamide) und anorganische Verdickungsmittel (Polykieselsäuren, Tonmineralien wie Montmorillonite, Zeolithe, Kieselsäuren).The agent according to the invention may further contain viscosity regulators. Suitable viscosity regulators are, for example, organic natural thickeners (agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, polyoses, guar flour, locust bean gum, starch, dextrins, gelatin, casein), organic modified natural substances (carboxymethylcellulose and other cellulose ethers, hydroxyethyl - and -propylcellulose and the like, core flour ethers), organic fully synthetic thickeners (polyacrylic and polymethacrylic compounds, vinyl polymers, polycarboxylic acids, polyethers, polyimines, polyamides) and inorganic thickeners (polysilicic acids, clay minerals such as montmorillonites, zeolites, silicas).
Zu den Polyacryl- und Polymethacryl-Verbindungen zählen beispielsweise die hochmolekularen mit einem Polyalkenylpolyether, insbesondere einem Allylether von Saccharose, Pentaerythrit oder Propylen, vernetzten Homopolymere der Acrylsäure (INCI-Bezeichnung gemäß International Dictionary of Cosmetic Ingredients der The Cosmetic, Toiletry, and Fragrance Association (CTFA): Carbomer), die auch als Carboxyvinylpolymere bezeichnet werden. Solche Polyacrylsäuren sind u.a. von der Fa. 3V Sigma unter dem Handelsnamen Polygel®, z.B. Polygel® DA, und von der Fa. BFGoodrich unter dem Handelsnamen Carbopol® erhältlich, z.B. Carbopol® 940 (Molekulargewicht ca. 4.000.000), Carbopol® 941 (Molekulargewicht ca. 1.250.000) oder Carbopol® 934 (Molekulargewicht ca. 3.000.000). Weiterhin fallen darunter folgende Acrylsäure-Copolymere: (i) Copolymere von zwei oder mehr Monomeren aus der Gruppe der Acrylsäure, Methacrylsäure und ihrer einfachen, vorzugsweise mit C-ι-4-Alkanolen gebildeten, Ester (INCI Acrylates Copolymer), zu denen etwa die Copolymere von Methacrylsäure, Butylacrylat und Methylmethacrylat (CAS-Bezeichnung gemäß Chemical Abstracts Service: 25035-69-2) oder von Butylacrylat und Methylmethacrylat (CAS 25852-37-3) gehören und die beispielsweise von der Fa. Rohm & Haas unter den Handelsnamen Aculyn® und Acusol® sowie von der Firma Degussa (Goldschmidt) unter dem Handelsnamen Tego® Polymer erhältlich sind, z.B. die anionischen nicht-assoziativen Polymere Aculyn® 22, Aculyn® 28, Aculyn® 33 (vernetzt), Acusol® 810, Acusol® 823 und Acusol® 830 (CAS 25852-37-3); (ii) vernetzte hochmolekulare Acrylsäurecopolymere, zu denen etwa die mit einem Allylether der Saccharose oder des Pentaerythrits vernetzten Copolymere von C10-30-Alkylacrylaten mit einem oder mehreren Monomeren aus der Gruppe der Acrylsäure, Methacrylsäure und ihrer einfachen, vorzugsweise mit C-|.4-Alkanolen gebildeten, Ester (INCI Acrylates/C 10-30 Alkyl Acrylate Crosspolymer) gehören und die beispielsweise von der Fa. BFGoodrich unter dem Handelsnamen Carbopol® erhältlich sind, z.B. das hydrophobierte Carbopol® ETD 2623 und Carbopol® 1382 (INCI Acrylates/C 10-30 Alkyl Acrylate Crosspolymer) sowie Carbopol® AQUA 30 (früher Carbopol® EX 473).Examples of polyacrylic and polymethacrylic compounds include the high molecular weight homopolymers of acrylic acid crosslinked with a polyalkenyl polyether, in particular an allyl ether of sucrose, pentaerythritol or propylene (INCI name according to the International Dictionary of Cosmetic Ingredients of The Cosmetic, Toiletry, and Fragrance Association (US Pat. CTFA): carbomers), also referred to as carboxyvinyl polymers. Such polyacrylic acids are obtainable inter alia from Fa. 3V Sigma under the tradename Polygel ® such as Polygel ® DA, and by the company. BFGoodrich under the tradename Carbopol ®, such as Carbopol ® 940 (molecular weight about 4,000,000), Carbopol ® 941 (molecular weight approximately 1,250,000) or Carbopol ® 934 (molecular weight approximately 3,000,000). Furthermore, the following acrylic acid copolymers are included: (i) Copolymers of two or more monomers from the group of acrylic acid, methacrylic acid and their simple, preferably with C-ι- 4 alkanols formed esters (INCI acrylates copolymer), to which about Copolymers of methacrylic acid, butyl acrylate and methyl methacrylate (CAS designation according to Chemical Abstracts Service: 25035-69-2) or of butyl acrylate and methyl methacrylate (CAS 25852-37-3) and the example of the Fa. Rohm & Haas under the trade name Aculyn polymer are available ® and Acusol ®, and from Degussa (Goldschmidt) under the trade name Tego ®, for example the anionic non-associative polymers Aculyn ® 22, Aculyn ® 28, Aculyn ® 33 (crosslinked), Acusol ® 810, Acusol ® 823 and Acusol ® 830 (CAS 25852-37-3); (ii) crosslinked high molecular weight acrylic acid copolymers, such as those crosslinked with an allyl ether of sucrose or pentaerythritol copolymers of C 10 - 30 alkyl acrylates with one or more monomers selected from the group of acrylic acid, methacrylic acid and their simple, preferably with C |. 4 -alkanols formed, esters (INCI Acrylates / C 10-30 Alkyl Acrylate Crosspolymer) and which are for example available from the company. BFGoodrich under the tradename Carbopol ®, for example hydrophobized Carbopol ® ETD 2623 and Carbopol ® 1382 (INCI Acrylates / C 10-30 alkyl acrylate Crosspolymer) and Carbopol AQUA ® 30 (formerly Carbopol ® EX 473).
Weitere Verdickungsmittel sind die Polysaccharide und Heteropolysaccharide, insbesondere die Polysaccharidgummen, beispielsweise Gummi arabicum, Agar, Alginate, Carrageene und ihre Salze, Guar, Guaran, Traganth, Gellan, Ramsan, Dextran oder Xanthan und ihre Derivate, z.B. propoxyliertes Guar, sowie ihre Mischungen. Andere Polysaccharidverdicker, wie Stärken oder Cellulosederivate, können alternativ, vorzugsweise aber zusätzlich zu einem Polysaccharidgummi eingesetzt werden, beispielsweise Stärken verschiedensten Ursprungs und Stärkederivate, z.B. Hydroxyethylstärke, Stärkephosphatester oder Stärkeacetate, oder Carboxymethylcellulose bzw. ihr Natriumsalz, Methyl-, Ethyl-, Hydroxyethyl-, Hydroxypropyl-, Hydroxypropyl-methyl- oder Hydroxyethyl-methyl-cellulose oder Celluloseacetat. Ein besonders bevorzugter Polysaccharidverdicker ist das mikrobielle anionische Heteropolysaccharid Xanthan Gum, das von Xanthomonas campestris und einigen anderen Spezies unter aeroben Bedingungen mit einem Molekulargewicht von 2-15x106 produziert wird und beispielsweise von der Fa. Kelco unter den Handelsnamen Keltrol® und Kelzan ® oder auch von der Firma Rhodia unter dem Handelsnamen Rhodopol® erhältlich ist.Further thickeners are the polysaccharides and heteropolysaccharides, in particular the polysaccharide gums, for example gum arabic, agar, alginates, carrageenans and their salts, guar, guar gum, tragacanth, gellan, Ramzan, dextran or xanthan and their derivatives, eg propoxylated guar, as well as their mixtures. Other polysaccharide thickeners, such as starches or cellulose derivatives, may alternatively or preferably be used in addition to a polysaccharide gum, for example starches of various origins and starch derivatives, for example hydroxyethyl starch, starch phosphate esters or starch acetates, or carboxymethylcellulose or its sodium salt, methyl, ethyl, hydroxyethyl, Hydroxypropyl, hydroxypropyl methyl or hydroxyethyl methyl cellulose or cellulose acetate. A particularly preferred polysaccharide thickener is the microbial anionic heteropolysaccharide xanthan gum, which is produced by Xanthomonas campestris and some other species under aerobic conditions with a molecular weight of 2-15x10 6 and for example, by Fa. Kelco under the trade names Keltrol ® and Kelzan ® or available from Rhodia under the trade name Rhodopol ®.
Als Verdickungsmittel können weiterhin Schichtsilikate eingesetzt werden. Hierzu zählen beispielsweise die unter dem Handelsnamen Laponite® erhältlichen Magnesium- oder Natrium-Magnesium- Schichtsilikate der Firma Solvay Alkali, insbesondere das Laponite® RD oder auch Laponite® RDS, sowie die Magnesiumsilikate der Firma Süd-Chemie, vor allem das Optigel® SH. Bei der Wahl des geeigneten Viskositätsregulators ist darauf zu achten, daß der transparente Eindruck des Reinigungsmittels erhalten bleibt, d.h. der Einsatz des Verdickungsmittels sollte nicht zur Eintrübung des Mittels führen. Die Menge an Viskositätsregulator beträgt üblicherweise bis zu 0,5 Gew.-%, vorzugsweise 0,001 bis 0,3 Gew.-%, insbesondere 0,01 bis 0,2 Gew.-%, äußerst bevorzugt 0,01 bis 0,15 Gew.-%. In einer besonders bevorzugten Ausführungsform ist das erfindungsgemäße Mittel jedoch frei von Viskositätsregulatoren, da diese auch zur unerwünschten Streifenbildung beitragen können.As thickeners, it is also possible to use phyllosilicates. These include, for example, available under the trade name Laponite ® magnesium or sodium-magnesium phyllosilicates from Solvay Alkali, in particular the Laponite ® RD or Laponite ® RDS, and the magnesium silicates Süd-Chemie, especially the Optigel ® SH. When selecting the suitable viscosity regulator, care must be taken to ensure that the transparent impression of the cleaning agent is retained, ie the use of the thickener should not lead to clouding of the agent. The amount of viscosity regulator is usually up to 0.5 wt .-%, preferably 0.001 to 0.3 wt .-%, in particular 0.01 to 0.2 wt .-%, most preferably 0.01 to 0.15 wt .-%. In a particularly preferred embodiment, however, the agent according to the invention is free from viscosity regulators, since these may also contribute to the undesirable streaking.
Daneben kann das erfindungsgemäße Mittel weitere der genannten Hilfs-und Zusatzstoffe enthalten. Der pH-Wert der erfindungsgemäßen Mittel kann über einen weiten Bereich variiert werden, bevorzugt ist jedoch ein Bereich von 2,5 bis 12. Für das Desinfektionsmittel ist dabei ein neutraler oder schwach saurer pH-Wert, vorzugsweise 6 bis 7,5, insbesondere 6,5 bis 7, bevorzugt. Desinfizierende Reinigungsmittel für harte Oberflächen haben vorzugsweise einen pH-Wert von 7,5 bis 10, vorzugsweise 8 bis 9,5, und Mittel zur Hautdesinfektion sind bevorzugt auf einen schwach sauren pH-Wert von 5,0 bis 6,0, vorzugsweise 5,5 eingestellt. Sofern Verdickungsmittel im erfindungsgemäßen Mittel eingesetzt werden, liegt der pH-Wert vorzugsweise im neutralen Bereich (pH 6,5 bis 7,5).In addition, the agent according to the invention may contain further of the auxiliaries and additives mentioned. The pH of the compositions of the invention can be varied over a wide range, but is preferably a range of 2.5 to 12. For the disinfectant is a neutral or slightly acidic pH, preferably 6 to 7.5, in particular 6 , 5 to 7, preferred. Desinfecting hard surface cleaners preferably have a pH of 7.5 to 10, preferably 8 to 9.5, and skin disinfectants are preferably of a weakly acidic pH of 5.0 to 6.0, preferably 5, 5 set. If thickeners are used in the composition according to the invention, the pH is preferably in the neutral range (pH 6.5 to 7.5).
Die erfindungsgemäßen Mittel werden vorzugsweise als vor der Anwendung entsprechend zu verdünnendes Konzentrat formuliert. Sie können durch Aufmischen unmittelbar aus ihren Rohstoffen, anschließendes Durchmischen und abschließendes Stehen des Mittels bis zur Blasenfreiheit hergestellt werden. Die erfindungsgemäßen Mittel werden vorzugsweise zur Reinigung harter Oberflächen verwendet. Harte Oberflächen im Sinne dieser Anmeldung sind dabei Fenster, Spiegel und weitere Glasoberflächen, Oberflächen aus Keramik, Kunststoff, Metall oder auch Holz sowie lackiertes Holz, die sich in Haushalt und Gewerbe finden, etwa Badkeramik, Küchenoberflächen oder Fußböden. Dabei wird das Reinigungsmittel vorzugsweise vor der Anwendung mit Wasser verdünnt.The compositions according to the invention are preferably formulated as concentrate to be diluted before use. They can be prepared by mixing directly from their raw materials, then mixing and final standing of the agent to freedom from bubbles. The agents according to the invention are preferably used for cleaning hard surfaces. Hard surfaces in the context of this application are windows, mirrors and other glass surfaces, surfaces made of ceramic, plastic, metal or wood and lacquered wood, which are found in household and commercial, such as bathroom ceramics, kitchen surfaces or floors. The cleaning agent is preferably diluted with water before use.
Ein weiterer Erfindungsgegenstand ist daher die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Reinigung harter Oberflächen nach dem Verdünnen.Another subject of the invention is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces after dilution.
Zur Reinigung harter Oberflächen mit dem erfindungsgemäßen Mittel hat sich dabei folgendes ein Verfahren bewährt, bei dem das erfindungsgemäße Reinigungsmittel zunächst mit Wasser verdünnt wird, die so entstandene Reinigungsflotte auf die zu reinigende Oberfläche aufgetragen wird, das Mittel anschließend unter Zuhilfenahme eines Tuchs, eines Schwamms oder eines anderen geeigneten Substrats auf der Oberfläche verteilt wird und schließlich trocknet. Noch ein weiterer Erfindungsgegenstand ist dementsprechend ein Verfahren zur Reinigung harter Oberflächen, bestehend aus den Schritten a) Herstellung einer Reinigungsflotte durch Verdünnen eines Reinigungsmittels gemäß einem der Ansprüche 1 bis 9 mit Wasser, b) Auftragen des verdünnten Reinigungsmittels auf die zu reinigende Oberfläche, c) Wischen mit einem Tuch, einem Schwamm, einem Leder oder einem anderen für diesen Zweck geeigneten Substrat, um das Mittel auf der gesamten Oberfläche zu verteilen, d) Trocknenlassen. For cleaning hard surfaces with the agent according to the invention, the following has proven a method in which the cleaning agent according to the invention is first diluted with water, the resulting cleaning liquor is applied to the surface to be cleaned, the agent then with the aid of a cloth, a sponge or of another suitable substrate is spread on the surface and finally dries. A further subject of the invention is accordingly a process for cleaning hard surfaces, comprising the steps of a) producing a cleaning liquor by diluting a cleaning agent according to one of claims 1 to 9 with water, b) applying the diluted cleaning agent to the surface to be cleaned, c) Wipe with a cloth, sponge, leather or other suitable substrate for this purpose to spread the agent over the entire surface; d) allow to dry.
Beispielhafte Zusammensetzungen:Exemplary compositions:
Es wurden erfindungsgemäße Reinigungsmittel E1 bis E4 formuliert, deren Zusammensetzung in der nachfolgenden Tabelle wiedergegeben ist (Mengenangaben in Gew.-%). Der pH-Wert wird durch Zugabe von Natriumhydroxid eingestellt.Detergents E1 to E4 according to the invention have been formulated, the composition of which is given in the table below (quantities in% by weight). The pH is adjusted by adding sodium hydroxide.
Figure imgf000014_0001
Figure imgf000014_0001
Daneben wurden die nicht erfindungsgemäßen Vergleichsformulierungen V1 bis V5 hergestellt. Der pH-Wert wurde ebenfalls durch Zugabe von Natriumhydroxid eingestellt, die Mengen sind wiederum in Gew.-% angegeben.In addition, the comparative formulations V1 to V5 not according to the invention were prepared. The pH was also adjusted by the addition of sodium hydroxide, the amounts are again indicated in wt .-%.
Figure imgf000014_0002
Die erfindungsgemäßen Mittel E1 bis E4 sowie die Vergleichsmittel V1 bis V5 wurden jeweils in verdünnter wässriger Lösung (12 g/l) einer Prüfung der Reinigungsleistung gemäß den Qualitäts- normen des Industrieverbands Putz- und Pflegemittel e.V. (IPP) unterzogen. Bei diesem Test wird eine mit Testschmutz (gealtertes Gemisch aus Öl, Kaolin und schwarzem Pigment) behandelte weiße Oberfläche mit einem mit dem zu prüfenden Produkt getränkten Tuch gewischt. Hierzu wird ein Mehrspurwischgerät eingesetzt. Das Reinigungsergebnis wird mit Hilfe eines Remissionsfarbmessgerätes gegen einen Weißstandard bestimmt.
Figure imgf000014_0002
The compositions E1 to E4 according to the invention and the comparison agents V1 to V5 were each subjected to a test of the cleaning performance in dilute aqueous solution (12 g / l) in accordance with the quality standards of the Industrieverband Putz- und Pflegemittel eV (IPP). In this test, a white surface treated with test soil (aged mixture of oil, kaolin and black pigment) is wiped with a cloth soaked with the product to be tested. For this purpose, a multi-track wiper device is used. The cleaning result is determined by means of a remission colorimeter against a white standard.
Die erfindungsgemäßen Mittel zeigten dabei im Vergleich zu den Vergleichsrezepturen V3 bis V5 eine deutliche Steigerung der Reinigungsleistung. V1 zeigte zwar eine vergleichbare Reinigungsleistung, enthält aber im Gegensatz zu den erfindungsgemäßen Mitteln ein nur schlecht anaerob abbaubares lineares Alkylbenzolsulfonattensid (LAS). The compositions of the invention showed a significant increase in the cleaning performance in comparison to the comparative formulations V3 to V5. Although V1 showed a comparable cleaning performance, but contains in contrast to the inventive compositions a poorly anaerobically degradable linear alkylbenzenesulfonate (LAS).

Claims

Patentansprüche claims
1. Wässriges Reinigungsmittel für harte Oberflächen, umfassend mindestens eine Fettsäure oder ein Salz derselben, dadurch gekennzeichnet, dass es weiterhin mindestens ein Alkylamido- alkylamin enthält.1. An aqueous hard surface cleaning composition comprising at least one fatty acid or a salt thereof, characterized in that it further contains at least one Alkylamido- alkylamine.
2. Reinigungsmittel gemäß Anspruch 1 , dadurch gekennzeichnet, dass das Alkylamidoalkylamin vorzugsweise ausgewählt ist aus der Gruppe umfassend Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Sodium Stearoamphoacetate, Sodium Cocoamphoacetate, Disodium Cocoamphodipropionate, Disodium Stearoamphodiacetate sowie Gemische derselben und insbesondere bevorzugt Disodium Cocoamphodiacetate (Natriumkokosampho- diacetat) ist.2. Cleaning agent according to claim 1, characterized in that the alkylamidoalkylamine is preferably selected from the group comprising Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Sodium Stearoamphoacetate, Sodium Cocoamphoacetate, Disodium Cocoamphodipropionate, Disodium Stearoamphodiacetate and mixtures thereof and particularly preferably Disodium Cocoamphodiacetate (Natriumkokosampho- diacetat) is.
3. Reinigungsmittel gemäß einem der Ansprüche 1 und 2, dadurch gekennzeichnet dass es Alkylamidoalkylamine vorzugsweise in Mengen von 0,1 bis 10 Gew.%, besonders bevorzugt 0,2 bis 5 Gew.% enthält.3. Cleaning agent according to one of claims 1 and 2, characterized in that it contains Alkylamidoalkylamine preferably in amounts of 0.1 to 10 wt.%, Particularly preferably 0.2 to 5 wt.%.
4. Reinigungsmittel gemäß einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass es weiterhin mindestens ein nichtionisches Tensid enthält.4. Cleaning agent according to one of the preceding claims, characterized in that it further contains at least one nonionic surfactant.
5. Reinigungsmittel gemäß Anspruch 4, dadurch gekennzeichnet, dass es vorzugsweise bis zu 10 Gew.-% eines oder mehrerer nichtionischer Tenside enthält, besonders bevorzugt 0,01 bis 5 Gew.-%.5. Cleaning agent according to claim 4, characterized in that it preferably contains up to 10 wt .-% of one or more nonionic surfactants, particularly preferably 0.01 to 5 wt .-%.
6. Reinigungsmittel gemäß einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass es mindestens ein Alkylpolyglycosid enthält.6. Cleaning agent according to one of the preceding claims, characterized in that it contains at least one alkylpolyglycoside.
7. Reinigungsmittel gemäß einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass es mindestens ein Aminoxid enthält.7. Cleaning agent according to one of the preceding claims, characterized in that it contains at least one amine oxide.
8. Reinigungsmittel gemäß einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass es frei ist von linearen Alkylbenzolsulfonattensiden.8. Cleaning agent according to one of the preceding claims, characterized in that it is free of linear alkylbenzenesulfonate surfactants.
9. Reinigungsmittel gemäß einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass es weitere, üblicherweise in Reinigungsmitteln eingesetzte Inhaltsstoffe enthält, vorzugsweise ausgewählt aus der Gruppe umfassend weitere Tenside, Basen, Säuren, Viskositäts- veränderer, Lösungsmittel, weitere Polymere, antibakterielle Wirkstoffe, Konservierungsstoffe, Lösungsvermittler, Komplexbildner, Enzyme, Farbstoffe, Duftstoffe sowie Gemische derselben. 9. cleaning agent according to one of the preceding claims, characterized in that it contains further, usually used in cleaning ingredients, preferably selected from the group comprising other surfactants, bases, acids, viscosity modifiers, solvents, other polymers, antibacterial agents, preservatives, Solubilizers, complexing agents, enzymes, dyes, fragrances and mixtures thereof.
10. Verwendung eines Reinigungsmittels gemäß einem der vorangehenden Ansprüche zur Reinigung harter Oberflächen nach dem Verdünnen.10. Use of a cleaning agent according to one of the preceding claims for cleaning hard surfaces after dilution.
11. Verfahren zur Reinigung harter Oberflächen, bestehend aus den Schritten a) Herstellung einer Reinigungsflotte durch Verdünnen eines Reinigungsmittels gemäß einem der Ansprüche 1 bis 9 mit Wasser, b) Auftragen des verdünnten Reinigungsmittels auf die zu reinigende Oberfläche, c) Wischen mit einem Tuch, einem Schwamm, einem Leder oder einem anderen für diesen Zweck geeigneten Substrat, um das Mittel auf der gesamten Oberfläche zu verteilen, d) Trocknenlassen. 11. A method for cleaning hard surfaces, comprising the steps of a) preparing a cleaning liquor by diluting a cleaning agent according to one of claims 1 to 9 with water, b) applying the diluted cleaning agent to the surface to be cleaned, c) wiping with a cloth, a sponge, a leather or other suitable substrate for this purpose to distribute the agent over the entire surface, d) allow to dry.
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EP2329003B1 (en) 2016-12-14
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