EP0729502A1 - Liquid detergent and cleaner containing combinations of enzymes - Google Patents

Liquid detergent and cleaner containing combinations of enzymes

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Publication number
EP0729502A1
EP0729502A1 EP95900124A EP95900124A EP0729502A1 EP 0729502 A1 EP0729502 A1 EP 0729502A1 EP 95900124 A EP95900124 A EP 95900124A EP 95900124 A EP95900124 A EP 95900124A EP 0729502 A1 EP0729502 A1 EP 0729502A1
Authority
EP
European Patent Office
Prior art keywords
weight
alkyl
composition according
water
nonionic surfactant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP95900124A
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German (de)
French (fr)
Other versions
EP0729502B1 (en
Inventor
Georg Meine
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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Publication of EP0729502A1 publication Critical patent/EP0729502A1/en
Application granted granted Critical
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Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • 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
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • 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
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38663Stabilised liquid enzyme compositions
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/38Cationic compounds
    • C11D1/42Amino alcohols or amino ethers
    • C11D1/44Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
    • 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
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/525Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
    • 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
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/526Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 are polyalkoxylated
    • 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
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D1/74Carboxylates or sulfonates esters of polyoxyalkylene glycols

Definitions

  • the invention relates to liquid detergents and cleaning agents which contain protease, amylase and cellulase and water-soluble and optionally water-insoluble builders and a nonionic surfactant component which consists essentially of alkyl or alkenyl glycoside.
  • enzymes or enzyme combinations to improve the cleaning action of detergents and cleaning agents is generally known in the field of detergents and cleaning agents.
  • the most commonly used enzymes include protease, amylase, cellulase and lipase. These enzymes can each have different properties from one another and can come from different sources.
  • the prior art also describes enzyme combinations which are intended to improve the cleaning action of the detergents and cleaning agents in the case of a wide variety of enzymatically degradable soils.
  • European patent application EP 0365103 discloses a detergent which contains an organic, nonionic surfactant and builder for this surfactant and an enzyme combination consisting of protease, amylase and cellulase.
  • European patent application EP 0425214 describes an enzyme-containing washing and cleaning agent which contains anionic and / or nonionic surfactants, preferably a builder and an enzyme combination of three enzymes, namely protease, amylase and either lipase or cellulase.
  • liquid detergent which, in addition to anionic and nonionic surfactants, contains an enzyme combination of protease and a second enzyme such as cellulase, which is stabilized with the aid of an aromatic borate ester.
  • Surfactants based on glucose and other sugars, the alkyl glycosides with long-chain alkyl groups, are non-ionic surfactants.
  • Detergents which contain alkyl glycosides in combination with at least one conventional anionic surfactant are described in European patent application EP 070074.
  • Detergents which contain alkyl glycosides and anionic surfactants are also known from European patent application EP 092877.
  • liquid detergents are known from European patent application EP 105556, which contain alkyl glycosides, certain other nonionic surfactants and anionic surfactants. From international patent application WO 86/2943, alkyl glycoside-containing liquid detergents are known which additionally contain conventional anionic surfactants.
  • the object of the present invention is to provide a washing and cleaning agent which ensures sufficient stability of the enzymes contained and has improved washing activity.
  • the invention relates to a detergent and cleaning agent containing surfactant, protease, amylase, cellulase and builder, which contains a nonionic surfactant component which comprises at least 50% by weight, in particular at least 80% by weight a glycoside of the formula (I)
  • R 1 is an alkyl or alkenyl radical having 8 to 22 carbon atoms
  • G is a glycose unit
  • n is a number from 1 to 10.
  • the agent according to the invention compared to the prior art, has similar and sometimes even better washing properties at lower doses and that the enzymes contained also have good activity even after prolonged storage.
  • glycosides suitable for incorporation into the surfactant mixtures according to the invention are compounds of the general formula I in which R * is an alkyl or alkenyl radical having 8 to 22 carbon atoms, G is a glycose unit and n is a number between 1 and 10.
  • R * is an alkyl or alkenyl radical having 8 to 22 carbon atoms
  • G is a glycose unit
  • n is a number between 1 and 10.
  • Such compounds and their preparation are described, for example, in European patent applications EP 092355, EP 301 298, EP 357969 and EP 362671 or US Pat. No. 3547828.
  • the glycoside component ((G) n in formula I) is an oligomer or polymer from naturally occurring aldose or ketose monomers, in particular glucose, mannose, fructose, galactose, talose, gulose, altrose, or alelose , Idose, ribose, arabinose, xylose and lyxose.
  • the oligomers consisting of such glycosidically linked monomers are characterized not only by the type of sugar they contain, but also by their number, the so-called degree of oligomerization.
  • the degree of oligo erization (n in formula I) generally assumes fractional numerical values as the quantity to be determined analytically; it is between 1 and 10, for the glycosides preferably used below 1.5, in particular between 1.2 and 1.4.
  • the preferred monomer building block is glucose because of its good availability.
  • the alkyl or alkenyl moiety (R 1 in formula I) of the glycosides contained in the agents according to the invention preferably also originates from easily accessible derivatives of renewable raw materials, in particular from fatty alcohols, although also their branched chain isomers, in particular so-called oxo alcohols. can be used to produce usable glycosides. Accordingly, the primary alcohols with linear octyl, decyl, dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof are particularly suitable.
  • the proportion of further nonionic surfactant present in addition to the glycoside is up to 50% by weight, preferably at most 25% by weight, in particular 0.5% by weight to 20% by weight, based on the total nonionic surfactant component.
  • the further nonionic surfactants that come into question include the alkoxylates, in particular the ethoxylates and / or propoxylates of saturated or mono- to polyunsaturated linear or branched-chain alcohols having 10 to 22 carbon atoms, preferably 12 to 18 carbon atoms.
  • the degree of alkoxylation of the alcohols is generally between 1 and 20, preferably between 3 and 10. They can be prepared in a known manner by reacting the corresponding alcohols with the corresponding alkylene oxides.
  • the derivatives of fatty alcohols are particularly suitable, although their branched chain isomers, in particular so-called oxo alcohols, can also be used to prepare usable alkoxylates.
  • the alkoxylates in particular the ethoxylates, of primary alcohols with linear, in particular dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof, can be used.
  • Corresponding alkoxylation products of alkylamines, vicinal diols and carboxamides which correspond to the alcohols mentioned with regard to the alkyl part can also be used.
  • Such a nonionic surfactant system consisting of glycoside of the formula (I) and optionally further nonionic surfactant, is preferably used in the agents according to the invention in amounts of 1% by weight to 50% by weight, in particular contain from 1 wt .-% to 40 wt .-%.
  • the agent according to the invention is a cleaning agent, for example a manual or machine dishwashing agent or a cleaning agent for hard surfaces, the nonionic surfactant content can also be lower and is then preferably 0.5% by weight. up to 20% by weight, in particular 0.9% by weight to 10% by weight.
  • the agents according to the invention can contain further surfactants, preferably synthetic anionic surfactants of the sulfate or sulfonate type, in amounts of preferably not more than 20% by weight, in particular from 0.1% by weight to 18% by weight based on total mean.
  • Synthetic anionic surfactants which are particularly suitable for use in the agents according to the invention are the alkyl and / or alkenyl sulfates with 8 to 22 carbon atoms which carry an alkali metal, ammonium or alkyl or hydroxyalkyl substituted ammonium ion as countercation.
  • the alkyl and alkenyl sulfates may be prepared be ⁇ by reacting the corresponding alcohol component with a Usually, for chen sulfating agent, 'particularly sulfur trioxide or chlorosulfonic acid, and subsequent neutralization with alkali metal, ammonium or alkyl relationship as hydroxyalkyl-substituted ammonium bases in bekann ⁇ ter manner .
  • Such alkyl and / or alkenyl sulfates are contained in the agents according to the invention preferably in amounts from 0.1% by weight to 20% by weight, in particular from 0.1% by weight to 18% by weight.
  • the sulfate-type surfactants that can be used also include the sulfated alkoxylation products of the alcohols mentioned, so-called ether sulfates.
  • ether sulfates preferably contain 2 to 30, in particular 4 to 10, ethylene glycol groups per molecule.
  • Suitable anionic surfactants of the sulfonate type include the a-sulfoesters obtainable by reacting fatty acid esters with sulfur trioxide and subsequent neutralization, in particular those derived from fatty acids having 8 to 22 carbon atoms, preferably 12 to 18 carbon atoms, and linear alcohols with 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, derived sulfonation products, and the sulfofatty acids resulting from these by formal saponification.
  • the weight ratio of glycoside to alkyl or alkenyl or ether sulfate is preferably 5: 1 to 1: 4, in particular 1: 1 to 1: 3.5, where Anionic surfactant with a linear, primary alkyl or alkenyl radical having 14 to 18 carbon atoms is particularly preferred.
  • soaps with saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, pal itic acid or stearic acid, and from natural fatty acid mixtures, for example coconut and palm kernels -, or Taig fatty acids, derived soaps are suitable.
  • those soap mixtures are preferred which are composed of 50% by weight to 100% by weight of saturated C 1 -C 6 fatty acid soaps and up to 50% by weight of oleic acid soap.
  • Soap is preferably contained in amounts of 0.1% by weight to 5% by weight. In particular, however, higher amounts of soap of up to 20% by weight can also be contained in liquid agents.
  • the washing and cleaning agent contains enzymes from the class of proteases, amylases and cellulases. Enzymes obtained from fungi or bacterial strains such as Bacillus subtilis, Bacillus licheniformis, Bacillus lentus and Streptomyces griseus are preferably used.
  • proteases which can be used in the agents according to the invention include the enzymes which can be obtained from microorganisms, in particular bacteria or fungi, with a pH optimum in the alkaline range, for example those from the international patent applications WO 92/07067, WO 91/02792, WO 88 / 03947 or WO 88/03946 or the European patent applications EP 471 265, EP 416967 or EP 394352 known proteases.
  • Protease is preferably used in the agent according to the invention in amounts such that the finished agent 100 PE / g to 15000 PE / g (protease units per gram, determined by the method described in Tenside 7, 125 (1970)), in particular 125 PE / g to 7500 PE / g and particularly preferably 150 PE / g to 4500 PE / g.
  • Suitable proteases are commercially available, for example under the names BLAP ( R ), Savinase ( R ), Esperase ( R ), Maxatase ( R ), 0ptimase ( R ) or Alcalase ( R ).
  • amylases which can be used in agents according to the invention include the enzymes which can be obtained from bacteria or fungi and which have a pH optimum, preferably in the alkaline range up to about pH 10.
  • Useful commercial products include TermamyH) and Maxamyl ( R ).
  • Amylase is preferably used in the agent according to the invention in such amounts that the finished agent 0.01 KNU / g to 3 KNU / g ("Kilo-Novo-Units" per gram according to the Novo standard method, where 1 KNU is the amount of enzyme that degrades 5.26 g of starch at pH 5.6 and 37 ° C, based on the method described by P.
  • the cellulase used according to the invention also belongs to the enzymes which can be obtained from bacteria or fungi and which have a pH optimum, preferably in the almost neutral to weakly alkaline pH range from 6 to 9.5.
  • Such cellulases are known, for example, from German patent applications DE 31 17250, DE 3207825, DE 3207847, DE 3322950 or European patent applications EP 265832, EP 269077, EP 270974, EP 273 125 and EP 339550.
  • the agent according to the invention are preferably used in the agent according to the invention in amounts such that the finished agent has a cellulolytic activity of 0.05 IU / g to 1.5 IU / g ("International Units" per gram, based on the enzymatic hydrolysis of Na Carboxymethyl cellulose at pH 9.0 and 40 ° C., as described in Agric. Biol. Chem. 53, 1275 (1989) by S. Ito et al.), In particular 0.07 IU / g to 1.4 IU / g and particularly preferably 0.1 IU / g to 1.3 IU / g.
  • Suitable commercial products are, for example, Celluzyme ( R ) from Novo Industri or KAC ( R ) from Kao.
  • the agent according to the invention preferably contains 5% by weight to 55% by weight, in particular 5 to 35% by weight, of water-soluble, organic and / or inorganic builders.
  • the water-soluble, organic builder substances include, in particular, those from the class of the polycarboxylic acids, in particular citric acid and sugar acids, and also polymeric acrylic acids, methacrylic acids, maleic acids and copolymers of these, which can also contain small amounts of polymerizable substances without carboxylic acid functionality in copolymerized form .
  • the relative molecular weight of the homopolymers is generally between 1000 and 100000, that of the copolymers between 2000 and 200000. preferably 50,000 to 120,000, based on free acid.
  • a particularly preferred acrylic acid-maleic acid copolymer has a relative molecular weight of 50,000 to 100,000.
  • Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinyl methyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of acid is at least 50% by weight.
  • Terpolymers which contain two carboxylic acids and / or their salts as monomers and vinyl alcohol and / or a vinyl alcohol derivative or a carbohydrate as the third monomer can also be used as water-soluble organic builder substances.
  • the first acidic monomer or its salt is derived from a monoethylenically unsaturated C3-Cs-carboxylic acid and preferably from a Cj-Ctj-monocarboxylic acid, in particular from (meth) acrylic acid.
  • the second acidic monomer or its salt may be a derivative of a Cj-C ⁇ -dicarboxylic acid, preferably a C j -Cs-dicarboxylic be, maleic acid being particularly preferred.
  • the third monomeric unit is formed from vinyl alcohol and / or preferably an esterified vinyl alcohol.
  • Vinyl alcohol derivatives which are an ester of short-chain carboxylic acids, for example of C1-C4 carboxylic acids, with vinyl alcohol are particularly preferred.
  • Preferred terpolymers contain 60% by weight to 95% by weight, in particular 70% by weight to 90% by weight of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, and maleic acid or Maleate and 5 wt .-% to 40 wt .-%, preferably 10 wt .-% to 30 wt .-% vinyl alcohol and / or vinyl acetate.
  • the second acidic monomer or its salt can also be a derivative of an allylsulfonic acid which, in the 2-position, has an alkyl radical, preferably a C 1 -C 4 -alkyl radical, or an aromatic radical which is preferably derived from benzene or benzene. Derives derivatives, is substituted.
  • Preferred terpolymers contain 40% by weight to 60% by weight, in particular 45 to 55% by weight of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, 10% by weight to 30% by weight %, preferably 15% by weight up to 25% by weight of methyl sulfonic acid or methyl sulfonate and as the third monomer 15% by weight to 40% by weight, preferably 20% by weight to 40% by weight of a carbohydrate.
  • This carbohydrate can be, for example, a mono-, di-, oligo- or polysaccharide, mono-, di- or oligosaccharides being preferred, sucrose being particularly preferred.
  • the use of the third monomer presumably creates predetermined breaking points in the polymer, which are responsible for the good biodegradability of the polymer.
  • These terpolymers can be produced in particular by processes which are described in German patent applications P 42 21 381.9 and P 43 00 772.4, and generally have a relative molecular weight between 1000 and 200000, preferably between 200 and 50,000 and in particular between 3000 and 10,000 . They can be used in particular for the production of liquid agents, in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions. All of the polycarboxylic acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali salts.
  • the finished agent preferably contains these organic builder substances in amounts of up to 40% by weight, in particular up to 25% by weight and particularly preferably from 1% by weight to 5% by weight.
  • alkali metal carbonates A. potassium hydrogen carbonates and alkali metal sulfates and mixtures thereof are suitable.
  • additional inorganic material can be present in amounts of up to 20% by weight, but is preferably absent entirely.
  • the agents according to the invention can also contain up to 15% by weight, in particular 0.1% by weight to 5% by weight, of water-insoluble inorganic builders.
  • Suitable known water-insoluble inorganic builders are, in particular, the known crystalline or amorphous alkali alumosilicate in detergent quality, in particular zeolite NaA and optionally NaX, and crystalline layered silicates which are described in European patent application EP 0164514.
  • the agents according to the invention can, if desired, set an acidic or weakly alkaline pH of in particular about 8.0 to 9.5 inches 1% by weight aqueous solution containing solid inorganic and / or organic acids or acidic salts, for example alkali hydrogen sulfates, succinic acid, adipic acid or glutaric acid and mixtures thereof.
  • Such acidic substances are preferably contained in the agents according to the invention in amounts of not more than 5% by weight, in particular from 0.1% by weight to 3% by weight, with amounts close to the above-mentioned upper limit especially for cleaning agents are interesting.
  • the agents according to the invention can contain further constituents customary in washing and cleaning agents.
  • These optional constituents include, in particular, abrasive substances, for example quartz powder, complexing agents for heavy metals, for example aminopolycarboxylic acids, aminohydroxypypolycarboxylic acids, polyphosphonic acids and / or aminopolyphosphonic acids, graying inhibitors, for example cellulose ethers, foam inhibitors, for example organopolysiloxane siloxanesiloxane and optical derivatives, paraffin sulfonic acid and derivatives .
  • abrasive substances for example quartz powder
  • complexing agents for heavy metals for example aminopolycarboxylic acids, aminohydroxypypolycarboxylic acids, polyphosphonic acids and / or aminopolyphosphonic acids
  • graying inhibitors for example cellulose ethers
  • foam inhibitors for example organopolysiloxane siloxanesiloxane and optical derivatives, paraffin sulfonic acid and derivatives
  • optical brighteners in particular compounds from the class of the substituted 4,4'-bis (2 , 4,6-triamino-s-triazinyl) -stilbene-2,2'disulfonic acids, up to 5% by weight, in particular 0.1% by weight to 2% by weight, of complexing agents for heavy metals, in particular aminoalkylenephosphonic acids and their salts, up to 3% by weight, in particular 0.5% by weight to 2% by weight, of graying inhibitors and up to 2% by weight, in particular 0.1% by weight to 1% by weight Contain foam inhibitors, the weight percentages each referring to the entire composition.
  • solvents which can be used in liquid compositions according to the invention are preferably those which are water-miscible. These include the lower alcohols, for example ethanol, propanol, isopropanol, and the isomeric butanols, glycerol, lower glycols, for example ethylene and propylene glycol, and the ethers which can be derived from the compound classes mentioned.
  • the water content of the compositions is preferably 10% by weight to 50% by weight and in particular 20% by weight to 40% by weight.
  • the compositions preferably contain 2 to 12% by weight and in particular 3 to 10% by weight of ethanol or any mixture of ethanol and glycerin.
  • the customary enzyme stabilizers which may be present include amino alcohols, for example mono-, di-, triethanol and propanolamine and their mixtures, lower carboxylic acids, as known, for example, from European patent applications EP 376705 and EP 378261, boric acid or alkali borates, boric acid Carboxylic acid combinations, as are known, for example, from European patent application EP 451 921, calcium salts, for example the calcium formic acid combination known from European patent EP 028865, magnesium salts, as known, for example, from European patent application EP 378262 , and / or sulfur-containing reducing agents, as known for example from European patent applications EP 080748 or EP 080223.
  • amino alcohols for example mono-, di-, triethanol and propanolamine and their mixtures
  • lower carboxylic acids as known, for example, from European patent applications EP 376705 and EP 378261
  • boric acid or alkali borates boric acid Carboxylic acid combinations
  • boric acid Carboxylic acid combinations
  • Suitable foam inhibitors include long-chain soaps, in particular behenic acid, fatty acid amides, paraffins, waxes, microcrystalline waxes, organopolysiloxanes and mixtures thereof, which may also contain microfine, optionally silanized or otherwise hydrophobized silica.
  • foam inhibitors are preferably bound to granular, water-soluble carrier substances, as described, for example, in German patent application DE 3436 194, European patent applications EP 262588, EP 301 414, EP 309931 or European patent EP 151 386.
  • the agent according to the invention can furthermore contain graying inhibitors.
  • Graying inhibitors have the task of keeping the dirt detached from the fiber suspended in the liquor and thus preventing the graying of the fibers.
  • Water-soluble colloids of mostly organic nature are suitable for this, for example the water-soluble salts of polymeric carboxylic acids, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or cellulose or salts of acidic sulfuric acid esters of cellulose or starch.
  • Water-soluble polyamides containing acidic groups are also suitable for this purpose. Soluble starch preparations and starch products other than those mentioned above can also be used, for example partially hydrolyzed starch.
  • the agent according to the invention can also contain further enzymes, for example oxidase, peroxidase and / or lipase.
  • the lipase is an enzyme that can be obtained from microorganisms, in particular bacteria or fungi. Such is known for example from European patent applications EP 204208, EP 214761, EP 258068, EP 407225 or international patent application WO 87/00859.
  • Useful commercially available lipases include Lipolase ' R ) and Lipozym ( R ).
  • Lipase is preferably used in the agent according to the invention in amounts such that the finished agent 10 LU / g to 10000 LU / g ("lipase activity units" per gram, determined via the enzymatic hydrolysis of tri-butyrin at 30 ° C. and pH 7 according to the method mentioned in EP 258068), in particular 80 LU / g to 5000 LU / g and particularly preferably 100 LU / g to 1000 LU / g.
  • a preferred embodiment comprises a liquid agent containing 5% by weight to 35% by weight of water-soluble organic builder, up to 15% by weight, in particular 0% by weight to 5% by weight of water-insoluble inorganic builder, up to 15% by weight, in particular 0.5% by weight to 10% by weight, of synthetic anionic surfactant, 1% by weight to 40% by weight of nonionic surfactant, up to 15% by weight, in particular 4% by weight to 12% by weight of soap and up to 30% by weight, in particular 1% by weight to 25% by weight of water and / or water-miscible solvent and up to 10% by weight, in particular 0 , 01 to 7.5 wt .-% enzyme stabilizer system.
  • liquid compositions of the present invention can be prepared by simply mixing the constituents or their premixes, which can be liquid or dissolved in water or in a solvent provided.
  • Table 1 lists the components of a liquid detergent according to the invention and a detergent from the prior art.
  • the detergents were prepared by thoroughly mixing the components listed in Table 1.
  • To check the cleaning performance washing tests were carried out with artificial soiling under conditions of use (drum washing machine Miele W 918, 2.0 kg of normally soiled laundry, water hardness) 16 ° d; Evaluation carried out by remission measurement at 460 nm, without UV).
  • the reflectance values given in Table 2 were determined as a double determination.
  • Amylase ⁇ 0.05 0.5
  • the enzyme stability in an agent according to the invention which had the composition described in Table 1, was determined.
  • the agent was stored for 3 months at room temperature.
  • the residual activities of the various enzymes in% of the starting activity are listed in Table 3.

Abstract

Disclosed is a liquid detergent and cleaner containing surfactant, protease, amylase, cellulase and builder as well as a nonionic surfactant component that consists of at least 50 wt.%, especially at least 80 wt.%, glycoside of the formula R<1>-O(G)n, where R<1> is an alkyl or alkenyl group with 8 to 22 C atoms, G is a glycose unit and n is a number from 1 to 10. The detergent and cleaner has excellent enzyme stability and improved detergent characteristics.

Description

Enzvmkombinationshaltioe flüssige Wasch- und Reinigungsmittel Enzvmkombinationshaltioe liquid washing and cleaning agents
Die Erfindung betrifft flüssige Wasch- und Reinigungsmittel, die Protease, Amylase und Cellulase und wasserlöslichen und gegebenenfalls wasserunlösli¬ chen Builder sowie eine nichtionische Tensidkomponente enthalten, die im we¬ sentlichen aus Alkyl- beziehungsweise Alkenylglykosid besteht.The invention relates to liquid detergents and cleaning agents which contain protease, amylase and cellulase and water-soluble and optionally water-insoluble builders and a nonionic surfactant component which consists essentially of alkyl or alkenyl glycoside.
Die Verwendung von Enzymen beziehungsweise Enzymkombinationen zur Verbesse¬ rung der Reinigungswirkung von Wasch- und Reinigungsmitteln ist auf dem Ge¬ biet der Wasch- und Reinigungsmittel allgemein bekannt. Zu den am häufigsten eingesetzten Enzymen zählen Protease, Amylase, Cellulase und Lipase. Diese Enzyme können jeweils untereinander unterschiedliche Eigenschaften aufweisen und aus verschiedenen Quellen stammem.The use of enzymes or enzyme combinations to improve the cleaning action of detergents and cleaning agents is generally known in the field of detergents and cleaning agents. The most commonly used enzymes include protease, amylase, cellulase and lipase. These enzymes can each have different properties from one another and can come from different sources.
Im Stand der Technik werden auch Enzymkombinationen beschrieben, welche die Reinigungswirkung der Wasch- und Reinigungsmittel bei verschiedensten enzyma- tisch abbaubaren Verschmutzungen verbessern sollen.The prior art also describes enzyme combinations which are intended to improve the cleaning action of the detergents and cleaning agents in the case of a wide variety of enzymatically degradable soils.
Die europäische Patentanmeldung EP 0365103 offenbart ein Waschmittel, wel¬ ches ein organisches, nichtionisches Tensid und Builder für dieses Tensid sowie eine Enzymkombination, bestehend aus Protease, Amylase und Cellulase, enthält.European patent application EP 0365103 discloses a detergent which contains an organic, nonionic surfactant and builder for this surfactant and an enzyme combination consisting of protease, amylase and cellulase.
In der europäischen Patentanmeldung EP 0425214 wird ein enzy haltiges Wasch- und Reinigungsmittel beschrieben, welches anionische und/oder nichtionische Tenside, bevorzugt einen Builder und eine Enzymkombination aus drei Enzymen, nämlich Protease, Amylase und entweder Lipase oder Cellulase, enthält.European patent application EP 0425214 describes an enzyme-containing washing and cleaning agent which contains anionic and / or nonionic surfactants, preferably a builder and an enzyme combination of three enzymes, namely protease, amylase and either lipase or cellulase.
Aus der internationalen Patentanmeldung WO 92/19708 ist ein flüssiges Wasch¬ mittel bekannt, das neben anionischen und nichtionischen Tensiden eine Enzym¬ kombination aus Protease und einem zweiten Enzym wie Cellulase enthält, wel¬ che mit Hilfe eines aromatischen Boratesters stabilisiert wird.From the international patent application WO 92/19708 a liquid detergent is known which, in addition to anionic and nonionic surfactants, contains an enzyme combination of protease and a second enzyme such as cellulase, which is stabilized with the aid of an aromatic borate ester.
Die internationale Patentanmeldung WO 93/11215 offenbart ein flüssiges Wasch¬ mittel, welches anionisches oder nichtionisches Tensid, Zitronensäure oder ein wasserlösliches Salz davon, Propandiol und Borsäure, Protease und Cellu¬ lase als aktive Komponenten enthält. Die Enzymkombination wird durch Propan¬ diol und Borsäure in der Weise stabilisiert, daß diese beiden Komponenten mit den anderen Bestandteilen vermischt werden, bevor die Zitronensäure oder deren Salz zugefügt wird. Ferner wird offenbart, daß ethoxylierte Tenside die De¬ naturierung von Cellulase vermeiden.International patent application WO 93/11215 discloses a liquid detergent containing anionic or nonionic surfactant, citric acid or contains a water-soluble salt thereof, propanediol and boric acid, protease and cellulose as active components. The enzyme combination is stabilized by propanediol and boric acid in such a way that these two components are mixed with the other constituents before the citric acid or its salt is added. It is also disclosed that ethoxylated surfactants avoid the denaturation of cellulase.
Tenside auf Basis von Glukose und anderen Zuckern, die Alkylglykoside mit langkettigen Alkylgruppen, gehören zu den nichtionischen Tensiden. Wasch¬ mittel, die Alkylglykoside in Kombination mit wenigstens einem üblichen an¬ ionischen Tensid enthalten, werden in der europäischen Patentanmeldung EP 070074 beschrieben. Waschmittel, die Alkylglykoside und Aniontenside ent¬ halten, sind auch aus der europäischen Patentanmeldung EP 092877 bekannt. Des weiteren sind aus der europäischen Patentanmeldung EP 105556 flüssige Waschmittel bekannt, die Alkylglykoside, bestimmte andere nichtionische Ten¬ side und anionische Tenside enthalten. Aus der internationalen Patentanmel¬ dung WO 86/2943 sind alkylglykosidhaltige Flüssigwaschmittel bekannt, die zu¬ sätzlich übliche Aniontenside enthalten.Surfactants based on glucose and other sugars, the alkyl glycosides with long-chain alkyl groups, are non-ionic surfactants. Detergents which contain alkyl glycosides in combination with at least one conventional anionic surfactant are described in European patent application EP 070074. Detergents which contain alkyl glycosides and anionic surfactants are also known from European patent application EP 092877. Furthermore, liquid detergents are known from European patent application EP 105556, which contain alkyl glycosides, certain other nonionic surfactants and anionic surfactants. From international patent application WO 86/2943, alkyl glycoside-containing liquid detergents are known which additionally contain conventional anionic surfactants.
Die vorstehend genannten enzymhaltigen Wasch- und Reinigungsmittel haben alle den Nachteil, daß die darin enthaltenden Enzyme nur eine begrenzte Stabilität aufweisen und die Wascheigenschaften sich bereits nach kurzen Lagerzeiten wesentlich verschlechtern. Dies gilt auch für Mittel, denen Enzymstabilisato¬ ren zugesetzt wurden.The above-mentioned enzyme-containing detergents and cleaning agents all have the disadvantage that the enzymes contained therein have only a limited stability and the washing properties deteriorate significantly after short storage times. This also applies to agents to which enzyme stabilizers have been added.
Aufgabe der vorliegenden Erfindung ist es, ein Wasch- und Reinigungsmittel zur Verfügung zu stellen, welches eine ausreichende Stabilität der enthalten¬ den Enzyme gewährleistet und eine verbesserte Waschaktivität aufweist.The object of the present invention is to provide a washing and cleaning agent which ensures sufficient stability of the enzymes contained and has improved washing activity.
Die Erfindung betrifft ein tensid-, protease-, amylase-, cellulase- und buil- derhaltiges Wasch- und Reinigungsmittel, das eine nichtionische Tensidkompo- nente enthält, die zu mindestens 50 Gew.-%, insbesondere zu mindestens 80 Gew.-% aus einem Glykosid der Formel (I)The invention relates to a detergent and cleaning agent containing surfactant, protease, amylase, cellulase and builder, which contains a nonionic surfactant component which comprises at least 50% by weight, in particular at least 80% by weight a glycoside of the formula (I)
^O.G.n (I) in der R1 einen Alkyl- oder Alkenylrest mit 8 bis 22 C-Atomen, G eine Gly¬ kose-Einheit und n eine Zahl von 1 bis 10 bedeuten, besteht.^ OGn (I) in which R 1 is an alkyl or alkenyl radical having 8 to 22 carbon atoms, G is a glycose unit and n is a number from 1 to 10.
Überraschenderweise wurde gefunden, daß das erfindungsgemäße Mittel vergli¬ chen mit dem Stand der Technik bei geringerer Dosierung eine ähnliche und teilweise sogar bessere Wascheigenschaften aufweist und daß die enthaltenen Enzyme auch nach längerer Lagerung noch eine gute Aktivität aufweisen.Surprisingly, it was found that the agent according to the invention, compared to the prior art, has similar and sometimes even better washing properties at lower doses and that the enzymes contained also have good activity even after prolonged storage.
Die zur Einarbeitung in die erfindungsgemäßen Tensidmischungen geeigneten Glykoside sind Verbindungen der allgemeinen Formel I, in der R* einen Alkyl- oder Alkenylrest mit 8 bis 22 C-Atomen, G eine Glykoseeinheit und n eine Zahl zwischen 1 und 10 bedeuten. Derartige Verbindungen und ihre Herstellung wer¬ den zum Beispiel in den europäischen Patentanmeldungen EP 092355, EP 301 298, EP 357969 und EP 362671 oder der US-amerikanischen Patentschrift US 3547828 beschrieben. Bei der Glykosidkomponente ((G)n in Formel I) han¬ delt es sich um Oligo- oder Polymere aus natürlich vorkommenden Aldose- oder Ketose-Monomeren, zu denen insbesondere Glucose, Mannose, Fruktose, Galaktose, Talose, Gulose, Altrose, Ällose, Idose, Ribose, Arabinose, Xylose und Lyxose gehören. Die aus derartigen glykosidisch verknüpften Monomeren bestehenden Oligomere werden außer durch die Art der in ihnen enthaltenen Zucker durch deren Anzahl, den sogenannten Oligomerisierungsgrad, charakterisiert. Der Oligo erisierungsgrad (n in der Formel I) nimmt als analytisch zu ermittelnde Größe im allgemeinen gebrochene Zahlenwerte an; er liegt bei Werten zwischen 1 und 10, bei den vorzugsweise eingesetzten Glykosiden unter einem Wert von 1,5, insbesondere zwischen 1,2 und 1,4. Bevorzugter Monomer-Baustein ist we¬ gen der guten Verfügbarkeit Glucose.The glycosides suitable for incorporation into the surfactant mixtures according to the invention are compounds of the general formula I in which R * is an alkyl or alkenyl radical having 8 to 22 carbon atoms, G is a glycose unit and n is a number between 1 and 10. Such compounds and their preparation are described, for example, in European patent applications EP 092355, EP 301 298, EP 357969 and EP 362671 or US Pat. No. 3547828. The glycoside component ((G) n in formula I) is an oligomer or polymer from naturally occurring aldose or ketose monomers, in particular glucose, mannose, fructose, galactose, talose, gulose, altrose, or alelose , Idose, ribose, arabinose, xylose and lyxose. The oligomers consisting of such glycosidically linked monomers are characterized not only by the type of sugar they contain, but also by their number, the so-called degree of oligomerization. The degree of oligo erization (n in formula I) generally assumes fractional numerical values as the quantity to be determined analytically; it is between 1 and 10, for the glycosides preferably used below 1.5, in particular between 1.2 and 1.4. The preferred monomer building block is glucose because of its good availability.
Der Alkyl- oder Alkenylteil (R1 in der Formel I) der in den erfindungsgemäßen Mitteln enthaltenen Glykoside stammt bevorzugt ebenfalls aus leicht zugängli¬ chen Derivaten nachwachsender Rohstoffe, insbesondere aus Fettalkoholen, ob¬ wohl auch deren verzweigtkettige Isomere, insbesondere sogenannte Oxoalko- hole, zur Herstellung verwendbarer Glykoside eingesetzt werden können. Ge¬ eignet sind demnach insbesondere die primären Alkohole mit linearen Octyl-, Decyl-, Dodecyl-, Tetradecyl-, Hexadecyl- oder Octadecylresten sowie deren Gemische. Besonders bevorzugte Alkylglykoside enthalten einen Kokosfettalkyl- rest, das heißt Mischungen mit im wesentlichen Rl=Dodecyl und Rl=Tetradecyl. Die Glykoside können herstellungsbedingt geringe Mengen, beispielsweise 1 bis 2 %, an nicht umgesetztem freiem Fettalkohol enthalten, was sich nicht nach¬ teilig auf die Eigenschaften der damit hergestellten Produkte auswirkt, son¬ dern bei Flüssigprodukten sogar vorteilhaft ist. Fettalkohole können auch als zusätzliche hautschonende Komponenten in Shampoos, Handwaschpasten etc. ein¬ gesetzt werden.The alkyl or alkenyl moiety (R 1 in formula I) of the glycosides contained in the agents according to the invention preferably also originates from easily accessible derivatives of renewable raw materials, in particular from fatty alcohols, although also their branched chain isomers, in particular so-called oxo alcohols. can be used to produce usable glycosides. Accordingly, the primary alcohols with linear octyl, decyl, dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof are particularly suitable. Particularly preferred alkyl glycosides contain a coconut fatty alkyl rest, ie mixtures with essentially Rl = dodecyl and Rl = tetradecyl. Due to the production process, the glycosides can contain small amounts, for example 1 to 2%, of unreacted free fatty alcohol, which does not have a disadvantageous effect on the properties of the products produced therewith, but is even advantageous in the case of liquid products. Fatty alcohols can also be used as additional skin-protecting components in shampoos, hand-washing pastes, etc.
Der Anteil an weiterem, neben dem Glykosid enthaltenem Niotensid beträgt bis zu 50 Gew.-%, vorzugsweise höchstens 25 Gew.-%, insbesondere 0,5 Gew.-% bis 20 Gew.-%, bezogen auf die gesamte nichtionische Tensidkomponente. Zu den in Frage kommenden weiteren nichtionischen Tensiden gehören die Alkoxylate, ins¬ besondere die Ethoxylate und/oder Propoxylate von gesättigten oder ein- bis mehrfach ungesättigten linearen oder verzweigtkettigen Alkoholen mit 10 bis 22 C-Atomen, vorzugsweise 12 bis 18 C-Atomen. Der Alkoxylierungsgrad der Al¬ kohole liegt dabei in der Regel zwischen 1 und 20, vorzugsweise zwischen 3 und 10. Sie können in bekannter Weise durch Umsetzung der entsprechenden Al¬ kohole mit den entsprechenden Alkylenoxiden hergestellt werden. Geeignet sind insbesondere die Derivate der Fettalkohole, obwohl auch deren verzweigtket- tige Isomere, insbesondere sogenannte Oxoalkohole, zur Herstellung verwendba¬ rer Alkoxylate eingesetzt werden können. Brauchbar sind demgemäß die Alkoxy¬ late, insbesondere die Ethoxylate, primärer Alkohole mit linearen, insbeson¬ dere Dodecyl-, Tetradecyl-, Hexadecyl- oder Octadecyl-Resten sowie deren Ge¬ mische. Außerdem sind entsprechende Alkoxylierungsprodukte von Alkylaminen, vicinalen Diolen und Carbonsäureamiden, die hinsichtlich des Alkylteils den genannten Alkoholen entsprechen, verwendbar. Darüber hinaus kommen die Ethy- lenoxid- und/oder Propylenoxid-Insertionsprodukte von Fettsäurealkylestern, wie sie gemäß dem in der internationalen Patentanmeldung WO 90/13533 ange¬ gebenen Verfahren hergestellt werden können, sowie Fettsäurepolyhydroxyamide, wie sie gemäß den Verfahren der US-amerikanischen Patentschriften US 1 985424, US 2016962 und US 2703798 sowie der internationalen Patent¬ anmeldung WO 92/06984 hergestellt werden können, in Betracht.The proportion of further nonionic surfactant present in addition to the glycoside is up to 50% by weight, preferably at most 25% by weight, in particular 0.5% by weight to 20% by weight, based on the total nonionic surfactant component. The further nonionic surfactants that come into question include the alkoxylates, in particular the ethoxylates and / or propoxylates of saturated or mono- to polyunsaturated linear or branched-chain alcohols having 10 to 22 carbon atoms, preferably 12 to 18 carbon atoms. The degree of alkoxylation of the alcohols is generally between 1 and 20, preferably between 3 and 10. They can be prepared in a known manner by reacting the corresponding alcohols with the corresponding alkylene oxides. The derivatives of fatty alcohols are particularly suitable, although their branched chain isomers, in particular so-called oxo alcohols, can also be used to prepare usable alkoxylates. Accordingly, the alkoxylates, in particular the ethoxylates, of primary alcohols with linear, in particular dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof, can be used. Corresponding alkoxylation products of alkylamines, vicinal diols and carboxamides which correspond to the alcohols mentioned with regard to the alkyl part can also be used. In addition, there are the ethylene oxide and / or propylene oxide insertion products of fatty acid alkyl esters, as can be prepared in accordance with the process specified in international patent application WO 90/13533, and fatty acid polyhydroxyamides, as in accordance with the processes in the US patents US 1 985424, US 2016962 and US 2703798 and the international patent application WO 92/06984 can be considered.
Derartiges nichtionisches Tensidsystem, bestehend aus Glykosid gemäß Formel (I) und gegebenenfalls weiterem nichtionischen Tensid, ist in den erfindungs¬ gemäßen Mitteln vorzugsweise in Mengen von 1 Gew.-% bis 50 Gew.-%, insbeson- dere von 1 Gew.-% bis 40 Gew.-% enthalten. Falls es sich bei dem erfindungs- gemäßen Mittel um ein Reinigungsmittel, beispielsweise ein manuelles oder ma¬ schinelles Geschirrspülmittel oder ein Reinigungsmittel für harte Oberflächen handelt, kann der Gehalt an nichtionischem Tensid auch geringer sein und liegt dann vorzugsweise bei 0,5 Gew.-% bis 20 Gew.-%, insbesondere 0,9 Gew.-% bis 10 Gew.-%.Such a nonionic surfactant system, consisting of glycoside of the formula (I) and optionally further nonionic surfactant, is preferably used in the agents according to the invention in amounts of 1% by weight to 50% by weight, in particular contain from 1 wt .-% to 40 wt .-%. If the agent according to the invention is a cleaning agent, for example a manual or machine dishwashing agent or a cleaning agent for hard surfaces, the nonionic surfactant content can also be lower and is then preferably 0.5% by weight. up to 20% by weight, in particular 0.9% by weight to 10% by weight.
Darüberhinaus können die erfindungsgemäßen Mittel weitere Tenside, vorzugs¬ weise synthetische Aniontenside des Sulfat- oder Sulfonat-Typs, in Mengen von vorzugsweise nicht über 20 Gew.-%, insbesondere von 0,1 Gew.-% bis 18 Gew.-%, jeweils bezogen auf gesamtes Mittel, enthalten. Als für den Einsatz in den erfindungsgemäßen Mitteln besonders geeignete synthetische Aniontenside sind die Alkyl- und/oder Alkenylsulfate mit 8 bis 22 C-Atomen, die ein Alkali-, Ammonium- oder Alkyl- beziehungsweise Hydroxyalkyl-substituiertes Ammoniumion als Gegenkation tragen, zu nennen. Bevorzugt sind die Derivate der Fettalko¬ hole mit insbesondere 12 bis 18 C-Atomen und deren verzweigtkettige Analoga, der sogenannten Oxoalkohole. Die Alkyl- und Alkenylsulfate können in bekann¬ ter Weise durch Reaktion der entsprechenden Alkoholkomponente mit einem übli¬ chen Sulfatierungsreagenz,' insbesondere Schwefeltrioxid oder Chlorsulfonsäure, und anschließende Neutralisation mit Alkali-, Ammonium- oder Alkyl- be¬ ziehungsweise Hydroxyalkyl-substituierten Ammoniumbasen hergestellt werden. Derartige Alkyl- und/oder Alkenylsulfate sind in den erfindungsgemäßen Mit¬ teln vorzugsweise in Mengen von 0,1 Gew.-% bis 20 Gew.-%, insbesondere von 0,1 Gew.-% bis 18 Gew.-% enthalten.In addition, the agents according to the invention can contain further surfactants, preferably synthetic anionic surfactants of the sulfate or sulfonate type, in amounts of preferably not more than 20% by weight, in particular from 0.1% by weight to 18% by weight based on total mean. Synthetic anionic surfactants which are particularly suitable for use in the agents according to the invention are the alkyl and / or alkenyl sulfates with 8 to 22 carbon atoms which carry an alkali metal, ammonium or alkyl or hydroxyalkyl substituted ammonium ion as countercation. The derivatives of fatty alcohols with in particular 12 to 18 carbon atoms and their branched-chain analogs, the so-called oxo alcohols, are preferred. The alkyl and alkenyl sulfates may be prepared be¬ by reacting the corresponding alcohol component with a Usually, for chen sulfating agent, 'particularly sulfur trioxide or chlorosulfonic acid, and subsequent neutralization with alkali metal, ammonium or alkyl relationship as hydroxyalkyl-substituted ammonium bases in bekann¬ ter manner . Such alkyl and / or alkenyl sulfates are contained in the agents according to the invention preferably in amounts from 0.1% by weight to 20% by weight, in particular from 0.1% by weight to 18% by weight.
Zu den einsetzbaren Tensiden vom Sulfat-Typ gehören auch die sulfatierten Alkoxylierungsprodukte der genannten Alkohole, sogenannte Ethersulfate. Vor¬ zugsweise enthalten derartige Ethersulfate 2 bis 30, insbesondere 4 bis 10, Ethylenglykol-Gruppen pro Molekül. Zu den geeigneten Aniontensiden vom Sul- fonat-Typ gehören die durch Umsetzung von Fettsäureestern mit Schwefeltrioxid und anschließender Neutralisation erhältlichen a-Sulfoester, insbesondere die sich von Fettsäuren mit 8 bis 22 C-Atomen, vorzugsweise 12 bis 18 C-Atomen, und linearen Alkoholen mit 1 bis 6 C-Atomen, vorzugsweise 1 bis 4 C-Atomen, ableitenden Sulfonierungsprodukte, sowie die durch formale Verseifung aus diesen hervorgehenden Sulfofettsäuren. Falls synthetisches Aniontensid vom Alkyl- beziehungsweise Alkenylsulfat- be¬ ziehungsweise Ethersulfattyp vorhanden ist, beträgt das GewichtsVerhältnis von Glykosid zu Alkyl- beziehungsweise Alkenyl- beziehungsweise Ethersulfat vorzugsweise 5:1 bis 1:4, insbesondere 1:1 bis 1:3,5, wobei Aniontensid mit einem linearen, primären Alkyl- beziehungsweise Alkenylrest mit 14 bis 18 C-Atomen besonders bevorzugt ist.The sulfate-type surfactants that can be used also include the sulfated alkoxylation products of the alcohols mentioned, so-called ether sulfates. Such ether sulfates preferably contain 2 to 30, in particular 4 to 10, ethylene glycol groups per molecule. Suitable anionic surfactants of the sulfonate type include the a-sulfoesters obtainable by reacting fatty acid esters with sulfur trioxide and subsequent neutralization, in particular those derived from fatty acids having 8 to 22 carbon atoms, preferably 12 to 18 carbon atoms, and linear alcohols with 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, derived sulfonation products, and the sulfofatty acids resulting from these by formal saponification. If synthetic anionic surfactant of the alkyl or alkenyl sulfate or ether sulfate type is present, the weight ratio of glycoside to alkyl or alkenyl or ether sulfate is preferably 5: 1 to 1: 4, in particular 1: 1 to 1: 3.5, where Anionic surfactant with a linear, primary alkyl or alkenyl radical having 14 to 18 carbon atoms is particularly preferred.
Als weitere tensidische Inhaltsstoffe, die dem erfindungsgemäßen Mittel zuge¬ setzt werden können, kommen Seifen in Betracht, wobei gesättigte Fettsäure¬ seifen, wie die Salze der Laurinsäure, Myristinsäure, Pal itinsäure oder Stearinsäure, sowie aus natürlichen Fettsäuregemischen, zum Beispiel Kokos-, Palmkern-, oder Taigfettsäuren, abgeleitete Seifen geeignet sind. Insbeson¬ dere sind solche Seifengemische bevorzugt, die zu 50 Gew.-% bis 100 Gew.-% aus gesättigten C^-Ciß-Fettsäureseifen und bis zu 50 Gew.-% aus Ölsäureseife zusammengesetzt sind. Vorzugsweise ist Seife in Mengen von 0,1 Gew.-% bis 5 Gew.- enthalten. Insbesondere in flüssigen Mitteln können jedoch auch höhere Seifenmengen von bis zu 20 Gew.-% enthalten sein.Other suitable surfactant ingredients that can be added to the agent according to the invention are soaps, with saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, pal itic acid or stearic acid, and from natural fatty acid mixtures, for example coconut and palm kernels -, or Taig fatty acids, derived soaps are suitable. In particular, those soap mixtures are preferred which are composed of 50% by weight to 100% by weight of saturated C 1 -C 6 fatty acid soaps and up to 50% by weight of oleic acid soap. Soap is preferably contained in amounts of 0.1% by weight to 5% by weight. In particular, however, higher amounts of soap of up to 20% by weight can also be contained in liquid agents.
Erfindungsgemäß enthält das Wasch- und Reinigungsmittel Enzyme aus der Klasse der Proteasen, Amylasen und Cellulasen. Vorzugsweise werden aus Pilzen oder Bakterienstämmen, wie Bacillus subtilis, Bacillus licheniformis, Bacillus lentus und Streptomyces griseus gewonnene enzymatische Wirkstoffe eingesetzt.According to the invention, the washing and cleaning agent contains enzymes from the class of proteases, amylases and cellulases. Enzymes obtained from fungi or bacterial strains such as Bacillus subtilis, Bacillus licheniformis, Bacillus lentus and Streptomyces griseus are preferably used.
Zu den in den erfindungsgemäßen Mitteln einsetzbaren Proteasen gehören die aus Mikroorganismen, insbesondere Bakterien oder Pilzen, gewinnbaren Enzyme mit einem pH-Optimum im alkalischen Bereich, beispielsweise die aus den in¬ ternationalen Patentanmeldungen WO 92/07067, WO 91/02792, WO 88/03947 oder WO 88/03946 oder den europäischen Patentanmeldungen EP 471 265, EP 416967 oder EP 394352 bekannten Proteasen. Protease wird im erfindungsgemäßen Mit¬ tel vorzugsweise in solchen Mengen eingesetzt, daß das fertige Mittel 100 PE/g bis 15000 PE/g (Protease-Einheiten pro Gramm, bestimmt nach der in Tenside 7, 125 (1970) beschriebenen Methode), insbesondere 125 PE/g bis 7500 PE/g und besonders bevorzugt 150 PE/g bis 4500 PE/g aufweist. Geeignete Proteasen sind im Handel erhältlich, beispielsweise unter den Namen BLAP(R), Savinase(R), Esperase(R), Maxatase(R), 0ptimase(R) oder Alcalase(R). Zu den in erfindungsgemäßen Mitteln einsetzbaren Amylasen gehören die aus Bakterien oder Pilzen gewinnbaren Enzyme, welche ein pH-Optimum vorzugsweise im alkalischen Bereich bis etwa pH 10 aufweisen. Brauchbare Handelsprodukte sind beispielsweise TermamyH ) und Maxamyl(R). Amylase wird im erfindungsge¬ mäßen Mittel vorzugseise in solchen Mengen eingesetzt, daß das fertige Mittel 0,01 KNU/g bis 3 KNU/g ("Kilo-Novo-Units" pro Gramm gemäß der Standard-Me¬ thode der Firma Novo, wobei 1 KNU die Enzymmenge ist, die 5,26 g Stärke bei pH 5,6 und 37°C abbaut, basierend auf der von P. Bernfeld in S.P. Colowick und N.D. Kaplan, Methods in Enzymology, Band 1, 1955, Seite 149 beschriebenen Methode), insbesondere 0,010 KNU/g bis 1,8 KNU/g und besonders bevorzugt 0,01 KNU/g bis 1,6 KNU/g aufweist.The proteases which can be used in the agents according to the invention include the enzymes which can be obtained from microorganisms, in particular bacteria or fungi, with a pH optimum in the alkaline range, for example those from the international patent applications WO 92/07067, WO 91/02792, WO 88 / 03947 or WO 88/03946 or the European patent applications EP 471 265, EP 416967 or EP 394352 known proteases. Protease is preferably used in the agent according to the invention in amounts such that the finished agent 100 PE / g to 15000 PE / g (protease units per gram, determined by the method described in Tenside 7, 125 (1970)), in particular 125 PE / g to 7500 PE / g and particularly preferably 150 PE / g to 4500 PE / g. Suitable proteases are commercially available, for example under the names BLAP ( R ), Savinase ( R ), Esperase ( R ), Maxatase ( R ), 0ptimase ( R ) or Alcalase ( R ). The amylases which can be used in agents according to the invention include the enzymes which can be obtained from bacteria or fungi and which have a pH optimum, preferably in the alkaline range up to about pH 10. Useful commercial products include TermamyH) and Maxamyl ( R ). Amylase is preferably used in the agent according to the invention in such amounts that the finished agent 0.01 KNU / g to 3 KNU / g ("Kilo-Novo-Units" per gram according to the Novo standard method, where 1 KNU is the amount of enzyme that degrades 5.26 g of starch at pH 5.6 and 37 ° C, based on the method described by P. Bernfeld in SP Colowick and ND Kaplan, Methods in Enzymology, Volume 1, 1955, page 149 ), in particular 0.010 KNU / g to 1.8 KNU / g and particularly preferably 0.01 KNU / g to 1.6 KNU / g.
Auch die erfindungsgemäß verwendete Cellulase gehört zu den aus Bakterien oder Pilzen gewinnbaren Enzymen, welche ein pH-Optimum vorzugsweise im fast neutralen bis schwach alkalischen pH-Bereich von 6 bis 9,5 aufweisen. Derar¬ tige Cellulasen sind beispielsweise aus den deutschen Offenlegungsschriften DE 31 17250, DE 3207825, DE 3207847, DE 3322950 oder den europäischen Patentanmeldungen EP 265832, EP 269077, EP 270974, EP 273 125 sowie EP 339550 bekannt. Sie werden im erfindungsgemäßen Mittel vorzugsweise in solchen Mengen eingesetzt, daß das fertige Mittel eine cellulolytische Akti¬ vität von 0,05 IU/g bis 1,5 IU/g ("International Units" pro Gramm, basierend auf der enzymatischen Hydrolyse von Na-Carböxymethylcellulose bei pH 9,0 und 40°C, wie in Agric. Biol. Chem. 53, 1275 (1989) von S. Ito et al. beschrie¬ ben), insbesondere 0,07 IU/g bis 1,4 IU/g und besonders bevorzugt 0,1 IU/g bis 1,3 IU/g aufweist. Geeignete Handelsprodukte sind beispielsweise Cellu- zyme(R) der Novo Industri oder KAC(R) von Kao.The cellulase used according to the invention also belongs to the enzymes which can be obtained from bacteria or fungi and which have a pH optimum, preferably in the almost neutral to weakly alkaline pH range from 6 to 9.5. Such cellulases are known, for example, from German patent applications DE 31 17250, DE 3207825, DE 3207847, DE 3322950 or European patent applications EP 265832, EP 269077, EP 270974, EP 273 125 and EP 339550. They are preferably used in the agent according to the invention in amounts such that the finished agent has a cellulolytic activity of 0.05 IU / g to 1.5 IU / g ("International Units" per gram, based on the enzymatic hydrolysis of Na Carboxymethyl cellulose at pH 9.0 and 40 ° C., as described in Agric. Biol. Chem. 53, 1275 (1989) by S. Ito et al.), In particular 0.07 IU / g to 1.4 IU / g and particularly preferably 0.1 IU / g to 1.3 IU / g. Suitable commercial products are, for example, Celluzyme ( R ) from Novo Industri or KAC ( R ) from Kao.
Das erfindungsgemäße Mittel enthält vorzugsweise 5 Gew.-% bis 55 Gew.-%, ins¬ besondere 5 bis 35 Gew.-%, wasserlöslichen, organischen und/oder anorgani¬ schen Builder. Zu den wasserlöslichen, organischen Buildersubstanzen gehören insbesondere solche aus der Klasse der Polycarbonsäuren, insbesondere Citro- nensäure und Zuckersäuren sowie polymere Acrylsäuren, Methacrylsäuren, Mal¬ einsäuren und Mischpolymere aus diesen, die auch geringe Anteile polymeri- sierbarer Substanzen ohne Carbonsäurefunktionalität einpolymerisiert enthal¬ ten können. Die relative Molekülmasse der Homopolymeren liegt im allgemeinen zwischen 1000 und 100000, die der Copolymeren zwischen 2000 und 200000, vor- zugsweise 50000 bis 120000, bezogen auf freie Säure. Ein besonders bevorzug¬ tes Acrylsäure-Maleinsäure-Copolymer weist eine relative Molekülmasse von 50000 bis 100000 auf. Geeignete, wenn auch weniger bevorzugte Verbindungen dieser Klasse sind Copolymere der Acrylsäure oder Methacrylsäure mit Vinyl- ethern, wie Vinylmethylethern, Vinylester, Ethylen, Propylen und Styrol, in denen der Anteil der Säure mindestens 50 Gew.-% beträgt.The agent according to the invention preferably contains 5% by weight to 55% by weight, in particular 5 to 35% by weight, of water-soluble, organic and / or inorganic builders. The water-soluble, organic builder substances include, in particular, those from the class of the polycarboxylic acids, in particular citric acid and sugar acids, and also polymeric acrylic acids, methacrylic acids, maleic acids and copolymers of these, which can also contain small amounts of polymerizable substances without carboxylic acid functionality in copolymerized form . The relative molecular weight of the homopolymers is generally between 1000 and 100000, that of the copolymers between 2000 and 200000. preferably 50,000 to 120,000, based on free acid. A particularly preferred acrylic acid-maleic acid copolymer has a relative molecular weight of 50,000 to 100,000. Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinyl methyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of acid is at least 50% by weight.
Als wasserlösliche organische Buildersubstanzen können auch Terpolymere ein¬ gesetzt werden, die als Monomere zwei Carbonsäuren und/oder deren Salze sowie als drittes Monomer Vinylalkohol und/oder ein Vinylalkohol-Derivat oder ein Kohlenhydrat enthalten. Das erste saure Monomer beziehungsweise deren Salz leitet sich von einer monoethylenisch ungesättigten C3-Cs-Carbonsäure und vorzugsweise von einer Cj-Ctj-Monocarbonsäure, insbesondere von (Meth)acryl- säure ab. Das zweite saure Monomer beziehungsweise dessen Salz kann ein Derivat einer Cj-Cβ-Dicarbonsäure, vorzugsweise einer Cj-Cs-Dicarbonsäure sein, wobei Maleinsäure besonders bevorzugt ist. Die dritte monomere Einheit wird in diesem Fall von Vinylalkohol und/oder vorzugsweise einem veresterten Vinylalkohol gebildet. Insbesondere sind Vinylalkohol-Derivate bevorzugt, welche einen Ester aus kurzkettigen Carbonsäuren, beispielsweise von C1-C4- Carbonsäuren, mit Vinylalkohol darstellen. Bevorzugte Terpolymere enthalten dabei 60 Gew.-% bis 95 Gew.-%, insbesondere 70 Gew.-% bis 90 Gew.-% (Meth)- acrylsäure beziehungsweise (Meth)acrylat, besonders bevorzugt Acrylsäure be¬ ziehungsweise Acrylat, und Maleinsäure beziehungsweise Maleat sowie 5 Gew.-% bis 40 Gew.-%, vorzugsweise 10 Gew.-% bis 30 Gew.-% Vinylalkohol und/oder Vinylacetat. Ganz besonders bevorzugt sind dabei Terpolymere, in denen das Gewichtsverhältnis (Meth)acrylsäure beziehungsweise (Meth)acrylat zu Malein¬ säure beziehungsweise Maleat zwischen 1:1 und 4:1, vorzugsweise zwischen 2:1 und 3:1 und insbesondere 2:1 und 2,5:1 liegt. Dabei sind sowohl die Mengen als auch die Gewichtsverhältnisse auf die Säuren bezogen. Das zweite saure Monomer beziehungsweise dessen Salz kann auch ein Derivat einer Allylsulfon- säure sein, die in 2-Stellung mit einem Alkylrest, vorzugsweise mit einem Cι-C4-Alkylrest, oder einem aromatischen Rest, der sich vorzugsweise von Ben¬ zol oder Benzol-Derivaten ableitet, substituiert ist. Bevorzugte Terpolymere enthalten dabei 40 Gew.-% bis 60 Gew.-%, insbesondere 45 bis 55 Gew.-% (Meth)acrylsäure beziehungsweise (Meth)acrylat, besonders bevorzugt Acryl¬ säure beziehungsweise Acrylat, 10 Gew.-% bis 30 Gew.-%, vorzugsweise 15 Gew.-% bis 25 Gew.-% Methailylsulfonsäure beziehungsweise Methailylsulfonat und als drittes Monomer 15 Gew.-% bis 40 Gew.-%, vorzugsweise 20 Gew.-% bis 40 Gew.-% eines Kohlenhydrats. Dieses Kohlenhydrat kann dabei beispielsweise ein Mono-, Di-, Oligo- oder Polysaccharid sein, wobei Mono-, Di- oder Oligosaccharide bevorzugt sind, besonders bevorzugt ist Saccharose. Durch den Einsatz des dritten Monomers werden vermutlich Sollbruchstellen in das Polymer eingebaut, die für die gute biologische Abbaubarkeit des Polymers verantwortlich sind. Diese Terpolymere lassen sich insbesondere nach Verfahren herstellen, die in den deutschen Patentanmeldungen P 42 21 381.9 und P 43 00 772.4 beschrieben sind, und weisen im allgemeinen eine relative Molekülmasse zwischen 1000 und 200000, vorzugsweise zwischen 200 und 50000 und insbesondere zwischen 3000 und 10000 auf. Sie können insbesondere zur Herstellung flüssiger Mittel, in Form wäßriger Lösungen, vorzugsweise in Form 30- bis 50-gewichtsprozentiger wäßriger Lösungen eingesetzt werden. Alle genannten Polycarbonsäuren werden in der Regel in Form ihrer wasserlöslichen Salze, insbesondere ihrer Alkali¬ salze, eingesetzt. Das fertige Mittel enthält diese organischen Buildersub- stanzen vorzugsweise in Mengen bis zu 40 Gew.-%, insbesondere bis zu 25 Gew.-% und besonders bevorzugt von 1 Gew.-% bis 5 Gew.-%.Terpolymers which contain two carboxylic acids and / or their salts as monomers and vinyl alcohol and / or a vinyl alcohol derivative or a carbohydrate as the third monomer can also be used as water-soluble organic builder substances. The first acidic monomer or its salt is derived from a monoethylenically unsaturated C3-Cs-carboxylic acid and preferably from a Cj-Ctj-monocarboxylic acid, in particular from (meth) acrylic acid. The second acidic monomer or its salt may be a derivative of a Cj-Cβ-dicarboxylic acid, preferably a C j -Cs-dicarboxylic be, maleic acid being particularly preferred. In this case, the third monomeric unit is formed from vinyl alcohol and / or preferably an esterified vinyl alcohol. Vinyl alcohol derivatives which are an ester of short-chain carboxylic acids, for example of C1-C4 carboxylic acids, with vinyl alcohol are particularly preferred. Preferred terpolymers contain 60% by weight to 95% by weight, in particular 70% by weight to 90% by weight of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, and maleic acid or Maleate and 5 wt .-% to 40 wt .-%, preferably 10 wt .-% to 30 wt .-% vinyl alcohol and / or vinyl acetate. Terpolymers in which the weight ratio (meth) acrylic acid or (meth) acrylate to maleic acid or maleate is between 1: 1 and 4: 1, preferably between 2: 1 and 3: 1 and in particular 2: 1 and 2.5: 1. Both the amounts and the weight ratios are based on the acids. The second acidic monomer or its salt can also be a derivative of an allylsulfonic acid which, in the 2-position, has an alkyl radical, preferably a C 1 -C 4 -alkyl radical, or an aromatic radical which is preferably derived from benzene or benzene. Derives derivatives, is substituted. Preferred terpolymers contain 40% by weight to 60% by weight, in particular 45 to 55% by weight of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, 10% by weight to 30% by weight %, preferably 15% by weight up to 25% by weight of methyl sulfonic acid or methyl sulfonate and as the third monomer 15% by weight to 40% by weight, preferably 20% by weight to 40% by weight of a carbohydrate. This carbohydrate can be, for example, a mono-, di-, oligo- or polysaccharide, mono-, di- or oligosaccharides being preferred, sucrose being particularly preferred. The use of the third monomer presumably creates predetermined breaking points in the polymer, which are responsible for the good biodegradability of the polymer. These terpolymers can be produced in particular by processes which are described in German patent applications P 42 21 381.9 and P 43 00 772.4, and generally have a relative molecular weight between 1000 and 200000, preferably between 200 and 50,000 and in particular between 3000 and 10,000 . They can be used in particular for the production of liquid agents, in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions. All of the polycarboxylic acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali salts. The finished agent preferably contains these organic builder substances in amounts of up to 40% by weight, in particular up to 25% by weight and particularly preferably from 1% by weight to 5% by weight.
Zusätzliche zum genannten anorganischen Builder können weitere wasserlösliche Substanzen in den erfindungsgemäßen Mittel eingesetzt werden. Geeignet sind in diesem Zusammenhang die Alkalicarbonate, A.kalihydrogencarbonate und Alka¬ lisulfate sowie deren Gemische. Derartiges zusätzliches anorganische Material kann in Mengen bis zu 20 Gew.-% vorhanden sein, fehlt jedoch vorzugsweise ganz.In addition to the inorganic builder mentioned, other water-soluble substances can be used in the agents according to the invention. In this context, the alkali metal carbonates, A. potassium hydrogen carbonates and alkali metal sulfates and mixtures thereof are suitable. Such additional inorganic material can be present in amounts of up to 20% by weight, but is preferably absent entirely.
Die erfindungsgemäßen Mittel können auch bis zu 15 Gew.-%, insbesondere 0,1 Gew.-% bis 5 Gew.-% wasserunlöslichen anorganischen Builder enthalten. Als geeignete wasserunlösliche anorganische Builder werden insbesondere die be¬ kannten kristallinen oder amorphen Alkalialumosilikatn in Waschmittelquali¬ tät, insbesondere Zeolith NaA und gegebenenfalls NaX, sowie kristalline Schichtsilikate, die in der europäischen Patentanmeldung EP 0164514 be¬ schrieben werden, eingesetzt.The agents according to the invention can also contain up to 15% by weight, in particular 0.1% by weight to 5% by weight, of water-insoluble inorganic builders. Suitable known water-insoluble inorganic builders are, in particular, the known crystalline or amorphous alkali alumosilicate in detergent quality, in particular zeolite NaA and optionally NaX, and crystalline layered silicates which are described in European patent application EP 0164514.
Die erfindungsgemäßen Mittel können zur Einstellung eines gewünschtenfalls sauren oder schwach alkalischen pH-Werts von insbesondere etwa 8,0 bis 9,5 in 1-gewichtsprozentiger wäßriger Lösung feste anorganische und/oder organische Säuren beziehungsweise saure Salze, beispielsweise Alkalihydrogensulfate, Bernsteinsäure, Adipinsäure oder Glutarsäure sowie deren Gemische, enthalten. Derartige saure Substanzen sind in den erfindungsgemäßen Mitteln vorzugsweise in Mengen nicht über 5 Gew.-%, insbesondere von 0,1 Gew.-% bis 3 Gew.-%, ent¬ halten, wobei Mengen nahe der genannten Obergrenze insbesondere für Reini¬ gungsmittel interessant sind.The agents according to the invention can, if desired, set an acidic or weakly alkaline pH of in particular about 8.0 to 9.5 inches 1% by weight aqueous solution containing solid inorganic and / or organic acids or acidic salts, for example alkali hydrogen sulfates, succinic acid, adipic acid or glutaric acid and mixtures thereof. Such acidic substances are preferably contained in the agents according to the invention in amounts of not more than 5% by weight, in particular from 0.1% by weight to 3% by weight, with amounts close to the above-mentioned upper limit especially for cleaning agents are interesting.
Zusätzlich können die erfindungsgemäßen Mittel weitere in Wasch- und Reini¬ gungsmitteln übliche Bestandteile enthalten. Zu diesen fakultativen Bestand¬ teilen gehören insbesondere Abrasivstoffe, beispielsweise Quarzmehl, Komplex¬ bildner für Schwermetalle, beispielsweise Aminopolycarbonsäuren, Aminohy- drodxypolycarbonsäuren, Polyphosphonsäuren und/oder Aminopolyphosphonsäuren, Vergrauungsinhibitoren, beispielsweise Celluloseether, Schauminhibitoren, beispielsweise Organopolysiloxane oder Paraffine, und optische Aufheller, beispielsweise Stilbendisulfonsäurederivate. Vorzugsweise sind in den er¬ findungsgemäßen Mitteln bis zu 1 Gew.-%, insbesondere 0,01 Gew.-% bis 0,5 Gew.-% optische Aufheller, insbesondere Verbindungen aus der Klasse der substituierten 4,4'-Bis(2,4,6-triamino-s-triazinyl)-stilben-2,2'disulfon- säuren, bis zu 5 Gew.-%, insbesondere 0,1 Gew.-% bis 2 Gew.-% Komplexbildner für Schwermetalle, insbesondere Aminoalkylenphosphonsäuren und deren Salze, bis zu 3 Gew.-%, insbesondere 0,5 Gew.-% bis 2 Gew.-% Vergrauungsinhibitoren und bis zu 2 Gew.-%, insbesondere 0,1 Gew.-% bis 1 Gew.-% Schauminhibitoren enthalten, wobei sich die genannten Gewichtsanteile jeweils auf das gesamte Mittel beziehen.In addition, the agents according to the invention can contain further constituents customary in washing and cleaning agents. These optional constituents include, in particular, abrasive substances, for example quartz powder, complexing agents for heavy metals, for example aminopolycarboxylic acids, aminohydroxypypolycarboxylic acids, polyphosphonic acids and / or aminopolyphosphonic acids, graying inhibitors, for example cellulose ethers, foam inhibitors, for example organopolysiloxane siloxanesiloxane and optical derivatives, paraffin sulfonic acid and derivatives . Preferably up to 1% by weight, in particular 0.01% by weight to 0.5% by weight, of optical brighteners, in particular compounds from the class of the substituted 4,4'-bis (2 , 4,6-triamino-s-triazinyl) -stilbene-2,2'disulfonic acids, up to 5% by weight, in particular 0.1% by weight to 2% by weight, of complexing agents for heavy metals, in particular aminoalkylenephosphonic acids and their salts, up to 3% by weight, in particular 0.5% by weight to 2% by weight, of graying inhibitors and up to 2% by weight, in particular 0.1% by weight to 1% by weight Contain foam inhibitors, the weight percentages each referring to the entire composition.
Lösungsmittel, die bei flüssigen Mitteln gemäß der Erfindung eingesetzt wer¬ den können, sind neben Wasser vorzugsweise solche, die wassermischbar sind. Zu diesen gehören die niederen Alkohole, beispielsweise Ethanol, Propanol, iso-Propanol, und die isomeren Butanole, Glycerin, niedere Glykole, bei¬ spielsweise Ethylen- und Propylenglykol, und die aus den genannten Verbin¬ dungsklassen ableitbaren Ether. Der Wassergehalt der Mittel beträgt vorzugs¬ weise 10 Gew.-% bis 50 Gew.-% und insbesondere 20 Gew.-% bis 40 Gew-%. Die Mittel enthalten vorzugsweise 2 bis 12 Gew.-% und insbesondere 3 bis 10 Gew.-% Ethanol oder ein beliebiges Gemisch aus Ethanol und Glycerin. Zu den gegebenenfalls vorhandenen üblichen Enzymstabilisatoren gehören Ami- noalkohole, beispielsweise Mono-, Di-, Triethanol- und -propanolamin und de¬ ren Mischungen, niedere Carbonsäuren, wie beispielsweise aus den europäischen Patentanmeldungen EP 376705 und EP 378261 bekannt, Borsäure beziehungsweise Alkaliborate, Borsäure-Carbonsäure-Kombinationen, wie sie beispielsweise aus der europäischen Patentanmeldung EP 451 921 bekannt sind, Calciumsalze, bei¬ spielsweise die aus der europäischen Patentschrift EP 028865 bekannte Ca- Ameisensäure-Kombination, Magnesiumsalze, wie beispielsweise aus der euro¬ päischen Patentanmeldung EP 378262 bekannt, und/oder schwefelhaltige Reduk¬ tionmittel, wie beispielsweise aus den europäischen Patentanmeldungen EP 080748 oder EP 080223 bekannt.In addition to water, solvents which can be used in liquid compositions according to the invention are preferably those which are water-miscible. These include the lower alcohols, for example ethanol, propanol, isopropanol, and the isomeric butanols, glycerol, lower glycols, for example ethylene and propylene glycol, and the ethers which can be derived from the compound classes mentioned. The water content of the compositions is preferably 10% by weight to 50% by weight and in particular 20% by weight to 40% by weight. The compositions preferably contain 2 to 12% by weight and in particular 3 to 10% by weight of ethanol or any mixture of ethanol and glycerin. The customary enzyme stabilizers which may be present include amino alcohols, for example mono-, di-, triethanol and propanolamine and their mixtures, lower carboxylic acids, as known, for example, from European patent applications EP 376705 and EP 378261, boric acid or alkali borates, boric acid Carboxylic acid combinations, as are known, for example, from European patent application EP 451 921, calcium salts, for example the calcium formic acid combination known from European patent EP 028865, magnesium salts, as known, for example, from European patent application EP 378262 , and / or sulfur-containing reducing agents, as known for example from European patent applications EP 080748 or EP 080223.
Zu den geeigneten Schauminhibitoren gehören langkettige Seifen, insbesondere Behensäure, Fettsäureamide, Paraffine, Wachse, Mikrokristallinwachse, Organo- polysiloxane und deren Gemische, die darüber hinaus mikrofeine, gegebenen¬ falls silanierte oder anderweitig hydrophobierte Kieselsäure enthalten kön¬ nen. Zum Einsatz in partikelförmigen erfindungsgemäßen Mitteln sind derartige Schauminhibitoren vorzugsweise an granuläre, wasserlösliche Trägersubstaπzen gebunden, wie beispielsweise in der deutschen Offenlegungsschrift DE 3436 194, den europäischen Patentanmeldungen EP 262588, EP 301 414, EP 309931 oder der europäischen Patentschrift EP 151 386 beschrieben.Suitable foam inhibitors include long-chain soaps, in particular behenic acid, fatty acid amides, paraffins, waxes, microcrystalline waxes, organopolysiloxanes and mixtures thereof, which may also contain microfine, optionally silanized or otherwise hydrophobized silica. For use in particulate compositions according to the invention, such foam inhibitors are preferably bound to granular, water-soluble carrier substances, as described, for example, in German patent application DE 3436 194, European patent applications EP 262588, EP 301 414, EP 309931 or European patent EP 151 386.
Ferner kann das erfindungsgemäße Mittel Vergrauungsinhibitoren enthalten. Vergrauungsinhibitoren haben die Aufgabe, den von der Faser abgelösten Schmutz in der Flotte suspendiert zu halten und so das Vergrauen der Fasern zu ver¬ hindern. Hierzu sind wasserlösliche Kolloide meist organischer Natur ge¬ eignet, beispielsweise die wasserlöslichen Salze polymerer Carbonsäuren, Leim, Gelatine, Salze von Ethercarbonsäuren oder Ethersulfonsäuren der Stärke oder der Cellulose oder Salze von sauren Schwefelsäureestern der Cellulose oder der Stärke. Auch wasserlösliche, saure Gruppen enthaltende Polyamide sind für diesen Zweck geeignet. Weiterhin lassen sich lösliche Stärkepräparate und andere als die obengenannten Stärkeprodukte verwenden, zum Beispiel teil- hydrolysierte Stärke. Na-Carboxymethylcellulose, Methylcellulose, Methyl- hydroxyethylcellulose und deren Gemische sowie Polyvinylpyrrolidon werden be¬ vorzugt eingesetzt. Zusätzlich zu den oben genannten Enzymen kann das erfindungsgemäße Mittel auch weitere Enzyme, beispielsweise Oxidase, Peroxidase und/oder Lipase ent¬ halten. Bei der Lipase handelt es sich um ein aus Mikroorganismen, insbeson¬ dere Bakterien oder Pilzen, gewinnbares Enzym. Ein solches ist beispielsweise aus den europäischen Patentanmeldungen EP 204208, EP 214761, EP 258068, EP 407225 oder der internationalen Patentanmeldung WO 87/00859 bekannt. Brauchbare im Handel erhältiche Lipasen sind beispielsweise Lipolase'R) und Lipozym(R). Lipase wird im erfindungsgemäßen Mittel vorzugsweise in solchen Mengen eingesetzt, daß das fertige Mittel 10 LU/g bis 10000 LU/g ("Lipase- activity Units" pro Gramm, bestimmt über die enzymatische Hydrolyse von Tri- butyrin bei 30°C und pH 7 nach der in EP 258068 genannten Methode), insbe¬ sondere 80 LU/g bis 5000 LU/g und besonders bevorzugt 100 LU/g bis 1000 LU/g aufweist.The agent according to the invention can furthermore contain graying inhibitors. Graying inhibitors have the task of keeping the dirt detached from the fiber suspended in the liquor and thus preventing the graying of the fibers. Water-soluble colloids of mostly organic nature are suitable for this, for example the water-soluble salts of polymeric carboxylic acids, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or cellulose or salts of acidic sulfuric acid esters of cellulose or starch. Water-soluble polyamides containing acidic groups are also suitable for this purpose. Soluble starch preparations and starch products other than those mentioned above can also be used, for example partially hydrolyzed starch. Na carboxymethyl cellulose, methyl cellulose, methyl hydroxyethyl cellulose and mixtures thereof and polyvinylpyrrolidone are preferably used. In addition to the above-mentioned enzymes, the agent according to the invention can also contain further enzymes, for example oxidase, peroxidase and / or lipase. The lipase is an enzyme that can be obtained from microorganisms, in particular bacteria or fungi. Such is known for example from European patent applications EP 204208, EP 214761, EP 258068, EP 407225 or international patent application WO 87/00859. Useful commercially available lipases include Lipolase ' R ) and Lipozym ( R ). Lipase is preferably used in the agent according to the invention in amounts such that the finished agent 10 LU / g to 10000 LU / g ("lipase activity units" per gram, determined via the enzymatic hydrolysis of tri-butyrin at 30 ° C. and pH 7 according to the method mentioned in EP 258068), in particular 80 LU / g to 5000 LU / g and particularly preferably 100 LU / g to 1000 LU / g.
Eine bevorzugte Ausführungsform umfaßt ein flüssiges Mittel, enthaltend 5 Gew.-% bis 35 Gew.-% wasserlöslichen organischen Builder, bis zu 15 Gew.-%, insbesondere 0 Gew.-% bis 5 Gew.-% wasserunlöslichen anorganischen Builder, bis zu 15 Gew.-%, insbesondere 0,5 Gew.-% bis 10 Gew.-% synthetisches Anion¬ tensid, 1 Gew.-% bis 40 Gew.-% nichtionisches Tensid, bis zu 15 Gew.-%, ins¬ besondere 4 Gew.-% bis 12 Gew.-% Seife und bis zu 30 Gew.-%, insbesondere 1 Gew.-% bis 25 Gew.-% Wasser und/oder wassermischbares Lösungsmittel sowie bis zu 10 Gew.-%, insbesondere 0,01 bis 7,5 Gew.-% EnzymstabilisatorSystem.A preferred embodiment comprises a liquid agent containing 5% by weight to 35% by weight of water-soluble organic builder, up to 15% by weight, in particular 0% by weight to 5% by weight of water-insoluble inorganic builder, up to 15% by weight, in particular 0.5% by weight to 10% by weight, of synthetic anionic surfactant, 1% by weight to 40% by weight of nonionic surfactant, up to 15% by weight, in particular 4% by weight to 12% by weight of soap and up to 30% by weight, in particular 1% by weight to 25% by weight of water and / or water-miscible solvent and up to 10% by weight, in particular 0 , 01 to 7.5 wt .-% enzyme stabilizer system.
Die flüssigen Mittel der vorliegenden Erfindung können durch einfaches Vermi¬ schen der Bestandteile oder deren Vorgemische, die flüssig oder in Wasser be¬ ziehungsweise einem vorgesehenen Lösungsmittel gelöst vorliegen können, her¬ gestellt werden.The liquid compositions of the present invention can be prepared by simply mixing the constituents or their premixes, which can be liquid or dissolved in water or in a solvent provided.
BeispieleExamples
In Tabelle 1 sind die Komponenten eines flüssigen Waschmittels gemäß der Er¬ findung und eines Waschmittels aus dem Stand der Technik aufgeführt. Die Waschmittel wurden durch gutes Vermischen der in Tabelle 1 aufgeführten Kom¬ ponenten hergestellt. Zur Überprüfung der Reinigungsleistung wurden Waschver¬ suche mit künstlichen Anschmutzungen unter Anwendungsbedingungen (Trommel¬ waschmaschine Miele W 918, 2,0 kg normal verschmutzte Wäsche, Wasserhärte 16 °d; Auswertung mittels Remissionsmessung bei 460 nm, ohne UV) durchge¬ führt. Es ergaben sich die in Tabelle 2 angegebenen Remissionswerte als Doppelbestimmung.Table 1 lists the components of a liquid detergent according to the invention and a detergent from the prior art. The detergents were prepared by thoroughly mixing the components listed in Table 1. To check the cleaning performance, washing tests were carried out with artificial soiling under conditions of use (drum washing machine Miele W 918, 2.0 kg of normally soiled laundry, water hardness) 16 ° d; Evaluation carried out by remission measurement at 460 nm, without UV). The reflectance values given in Table 2 were determined as a double determination.
Tabelle 1: Zusammensetzunα TGew.-%1Table 1: Composition TGew .-% 1
gemäß deraccording to the
Vergleich ErfindungComparison invention
Fettsäuremonoglycerida) 0,5Fatty acid monoglyceride a ) 0.5
Fettsäure'') — 5Fatty acid '') - 5
Fettsäure0) 8 —Fatty acid 0 ) 8 -
Fettsäureseife^) 6 —Fatty acid soap ^) 6 -
KOH bis pH= 8,0KOH to pH = 8.0
NaOH bis pH= 8,2 —NaOH to pH = 8.2 -
Alkylethoxylate) 12 20Alkyl ethoxylate e ) 12 20
AlkylglykosidO 1,5 20Alkyl glycoside O 1.5 20
AlkylsulfatS) 4,5 --Alkyl sulfate S) 4.5 -
Alkylsulfat") — 4,6Alkyl sulfate ") - 4.6
Citronensäure 0,5 —Citric acid 0.5 -
Ethanol 6 5Ethanol 6 5
Glycerin 5 —Glycerin 5 -
1,2-Propylenglykol — 81,2-propylene glycol - 8
Proteasei) 0,5 —Proteasei) 0.5 -
Protease^) — 1Protease ^) - 1
Amylase^) 0,05 0,5Amylase ^) 0.05 0.5
Cellulase1") — 1Cellulase 1 ") - 1
Duftstoff 0,48 2 opt. Aufheller 0,48 —Fragrance 0.48 2 opt. Brightener 0.48 -
Pigment 0,58 —Pigment 0.58 -
Wasser Rest RestWater rest rest
a) Fettsäuremonoglycerid (Cutina(R) AGS, Hersteller Henkel) b) Ci2-Ci8-Fettsäure auf Basis von Kokosöl (Edenor(R) K 12-18, Hersteller Henkel) c) Fraktionierte Ci2-Fettsäure auf Basis Kokos-/Palmkernöl (Edenor(R) C12, Hersteller Henkel) d) Fettsäure auf Basis von Palmkernöl (Edenor(R) PK 1805, Hersteller Henkel) e) Ci2/l8"|:e't'tal'ohol, 7-fach ethoxyliert f) Ci2/i4-Alkylglycosid, Polymerisationsgrad 1,4 g) Ci2/14-Alkylsulfat (Texapon(R) LS 35, Hersteller Henkel) h) Ci6/i8-Alkylsulfat (Sulfopon(R) K 35, Hersteller Henkel) i) Protease (Alkalase(R) 2,5 LDX, Hersteller Novo) k) Protease (BLAP 280 L, Hersteller Biozym)a) Fatty acid monoglyceride (Cutina ( R ) AGS, manufacturer Henkel) b ) Ci2-Ci8 fatty acid based on coconut oil (Edenor ( R ) K 12-18, manufacturer Henkel) c) Fractionated Ci2 fatty acid based on coconut / palm kernel oil (Edenor ( R ) C12, manufacturer Henkel) d) Fatty acid based on palm kernel oil (Edenor ( R ) PK 1805, manufacturer Henkel) e) Ci2 / l8 " |: e ' t 'ta l'ohol, 7 times ethoxylated f) Ci2 / i4-alkyl glycoside of polymerization 1.4 g) Ci2 / 14-alkyl sulphate (Texapon (R) LS 35, a product of Henkel) h) Ci6 / i8-alkyl sulfate (Sulfopon ( R ) K 35, manufacturer Henkel) i) protease (Alkalase ( R ) 2.5 LDX, manufacturer Novo) k) protease (BLAP 280 L, manufacturer Biozym)
1) Amylase (Termamyl(R) 300 LDX, Hersteller Novo) m) Cellulase (Celluzyme(R) 1,0 L, Hersteller Novo)1) Amylase (Termamyl ( R ) 300 LDX, manufacturer Novo) m) Cellulase (Celluzyme ( R ) 1.0 L, manufacturer Novo)
Tabelle 2: Remission der gewaschenen Testgewebe T%.Table 2: Remission of the washed test fabrics T%.
Mittel Dosierung Remission bei AnschmutzungMedium dosage remission when soiled
(g) SH/B1 SH/BV2 SH/PBV3 SH/P4 (g) SH / B 1 SH / BV2 SH / PBV3 SH / P 4
gemäß der 40 63,2 63,8 56,4 65,2according to 40 63.2 63.8 56.4 65.2
Erfindunginvention
Vergleich 80 57,4 63,3 55,5 66,3Comparison 80 57.4 63.3 55.5 66.3
Legende:Legend:
1 = Staub/Hautfett auf Baumwolle1 = dust / skin fat on cotton
2 = " auf Baumwolle, veredelt2 = "on cotton, refined
3 = " auf Polyester/Baumwoll-Mischgewebe, veredelt3 = "on polyester / cotton blend, refined
4 = " auf Polyester Mittel Dosierung Remission bei Anschmutzung4 = "on polyester Medium dosage remission when soiled
(g) LS1/PBV5 LS3/PBV6 WT/PBV7 MU2/PBV8(g) LS1 / PBV5 LS3 / PBV6 WT / PBV7 MU2 / PBV8
gemäß der 40 48,4 56,3 54,0 49,7according to 40 48.4 56.3 54.0 49.7
Erfindunginvention
Vergleich 80 49,1 58,7 56,6 56,4Comparison 80 49.1 58.7 56.6 56.4
Legende:Legend:
5,6 = Lippenstift 1 und 3 auf Polyester/Baumwollemischgewebe, veredelt5,6 = lipstick 1 and 3 on polyester / cotton blend, refined
7 = Wimperntusche auf Polyester/Baumwollemischgewebe, veredelt7 = mascara on polyester / cotton blend, refined
8 = Make Up auf Polyester/Baumwollemischgewebe, veredelt8 = Make-up on polyester / cotton blend, refined
Mittel Dosierung Remission bei AnschmutzungMedium dosage remission when soiled
(g) RF4/B9 RF4/BV10 RF4/PBV*!(g) RF4 / B 9 RF4 / BV 1 0 RF4 / PBV *!
gemäß der 40 62,1 61,3 56,5 Erfindungaccording to the 40 62.1 61.3 56.5 invention
Vergleich 80 60,4 62,1 54,2Comparison 80 60.4 62.1 54.2
Legende:Legend:
9 = Ruß/Fett auf Baumwolle9 = soot / fat on cotton
10 = " auf Baumwolle, veredelt10 = "on cotton, refined
11 = " auf Polyester/Baumwollemischgewebe, veredelt 11 = "on polyester / cotton blend, refined
Mittel Dosierung Remission bei AnschmutzungMedium dosage remission when soiled
(g) MR/B12 BMR/B13 ER/B14 MK/B^(g) MR / B 12 BMR / B 13 ER / B 14 MK / B ^
gemäß der 40 48,4 56,3 54,0 49,7according to 40 48.4 56.3 54.0 49.7
Erfindunginvention
Vergleich 80 49,1 58,7 56,6 56,4Comparison 80 49.1 58.7 56.6 56.4
Legende:Legend:
12 = Milch/Ruß auf Baumwolle12 = milk / soot on cotton
13 = Blut/Milch/Ruß auf Baumwolle13 = blood / milk / soot on cotton
14 = Eiweiß/Ruß auf Baumwolle14 = protein / soot on cotton
15 = Milch/Kakao auf Baumwolle15 = milk / cocoa on cotton
Die Enzymstabilität in einem erfindungsgemäßen Mittel, welches die in Tabelle 1 beschriebene Zusammensetzung aufwies, wurde bestimmt. Dazu wurde das Mittel 3 Monate bei Raumtemperatur gelagert. Die Restaktivitäten der verschiedenen Enzyme in % der Ausgangsaktivität sind in Tabelle 3 aufgeführt.The enzyme stability in an agent according to the invention, which had the composition described in Table 1, was determined. The agent was stored for 3 months at room temperature. The residual activities of the various enzymes in% of the starting activity are listed in Table 3.
Tabelle 3: Restaktivität der Enzyme nach 3 Monaten Lagerung (%)Table 3: Remaining activity of the enzymes after 3 months storage (%)
Protease Cellulase Amylase Restaktivität 90 53 97 Protease cellulase amylase residual activity 90 53 97

Claims

Patentansprüche claims
1. Flüssiges tensid-, protease-, amylase-, cellulase- und builderhaltiges Wasch- und Reinigungsmittel, das eine nichtionische Tensidkomponente ent¬ hält, die zu mindestens 50 Gew.-%, insbesondere zu mindestens 80 Gew.-% aus einem Glykosid der Formel (I)1. Liquid detergent and protease, protease, amylase, cellulase and builder-containing detergent which contains a nonionic surfactant component containing at least 50% by weight, in particular at least 80% by weight, of a glycoside of Formula (I)
Rl-0(G)n (I) Rl -0 (G) n (I)
in der R einen Alkyl- oder Alkenylrest mit 8 bis 22 C-Atomen, G eine Glykose-Einheit und n eine Zahl von 1 bis 10 bedeuten, besteht.in which R is an alkyl or alkenyl radical having 8 to 22 carbon atoms, G is a glycose unit and n is a number from 1 to 10.
2. Mittel nach Anspruch 1, dadurch gekennzeichnet, daß die nichtionische Tensidkomponente zu mindestens 80 Gew.-% aus einem Glykosid der Formel (I) besteht und nebem diesem als weiteres Niotensid Fettalkylpolyalkoxy- lat, insbesondere -ethoxylat und/oder -propoxylat, Fettsäurepolyhydroxy- amid und/oder Ethoxylierungs- und/oder Propoxylierungsprodukt von Fett- alkylaminen, vicinalen Diolen, Fettsäurealkylestern und/oder Fettsäure- amiden enthält.2. Composition according to claim 1, characterized in that the nonionic surfactant component consists of at least 80 wt .-% of a glycoside of the formula (I) and besides this as a further nonionic surfactant fatty alkyl polyalkoxy lat, especially ethoxylate and / or propoxylate, fatty acid polyhydroxy - Contains amide and / or ethoxylation and / or propoxylation product of fatty alkylamines, vicinal diols, fatty acid alkyl esters and / or fatty acid amides.
3. Mittel nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß der Anteil an weiterem, neben dem Glykosid enthaltenem Niotensid höchstens 25 Gew.-%, insbesondere 0,5 Gew.-% bis 20 Gew.-%, bezogen auf das fertige Mittel, beträgt.3. Composition according to claim 1 or 2, characterized in that the proportion of further, in addition to the glycoside contained nonionic surfactant at most 25 wt .-%, in particular 0.5 wt .-% to 20 wt .-%, based on the finished agent , is.
4. Mittel nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß es 5 Gew.-% bis 55 Gew.- wasserlöslichen Builder, Protease in einer solchen Menge, daß die Aktivität 100 PE/g bis 15000 PE/g, insbesondere 125 PE/g bis 7500 PE/g, bezogen auf das gesamte Mittel, beträgt, Amylase in einer solchen Menge, daß die Aktivität 0,01 KNU/g bis 3 KNU/g, insbesondere 0,01 KNU/g bis 1,8 KNU/g, bezogen auf das gesamte Mittel, beträgt und Cellulase in einer solchen Menge, daß die Aktivität 0,05 IU/g bis 1,5 IU/g, insbesondere 0,07 IU/g bis 1,4 IU/g, bezogen auf das gesamte Mittel, beträgt, bis zu 20 Gew.- , insbesondere 0,1 Gew.-% bis 18 Gew.-% synthetisches Aniontensid und 1 Gew.-% bis 50 Gew.-% nichtionische Ten¬ sidkomponente enthält. 4. Composition according to one of claims 1 to 3, characterized in that there are 5 wt .-% to 55 wt .-% water-soluble builder, protease in such an amount that the activity 100 PE / g to 15000 PE / g, in particular 125 PE / g to 7500 PE / g, based on the total agent, amylase in such an amount that the activity 0.01 KNU / g to 3 KNU / g, in particular 0.01 KNU / g to 1.8 KNU / g, based on the total agent, and cellulase in such an amount that the activity based on 0.05 IU / g to 1.5 IU / g, in particular 0.07 IU / g to 1.4 IU / g based on the total agent, contains up to 20% by weight, in particular 0.1% by weight to 18% by weight, of synthetic anionic surfactant and 1% by weight to 50% by weight of nonionic surfactant component.
5. Mittel nach Anspruch 4, dadurch gekennzeichnet, daß das Aniontensid aus den Alkyl- beziehungsweise Alkenylsulfaten und/oder den Alkyl- beziehungs¬ weise Alkenylethersulfaten ausgewählt wird, in denen die Alkyl- be¬ ziehungsweise Alkenylgruppe 8 bis 22, insbesondere 12 bis 18 C-Atome be¬ sitzt.5. A composition according to claim 4, characterized in that the anionic surfactant is selected from the alkyl or alkenyl sulfates and / or the alkyl or alkenyl ether sulfates in which the alkyl or alkenyl group is 8 to 22, in particular 12 to 18 C. -Atoms sits.
6. Mittel nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß es 5 Gew.-% bis 35 Gew.-% wasserlöslichen organischen Builder, bis zu 15 Gew.-%, insbesondere 0,1 Gew.-% bis 5 Gew.-% wasserunlöslichen anorga¬ nischen Builder, bis zu 15 Gew.- , insbesondere 0,5 Gew.-% bis 10 Gew.-% synthetisches Aniontensid, 1 Gew.-% bis 40 Gew.-% nichtionisches Tensid, bis zu 15 Gew.-%, insbesondere 4 Gew.-% bis 12 Gew.-% Seife und bis zu 30 Gew.-%, insbesondere 1 Gew.-% bis 25 Gew.-% Wasser und/oder wasser¬ mischbares Lösungsmittel sowie bis zu 10 Gew.-%, insbesondere 0,01 Gew.-% bis 7,5 Gew.- Enzymstabilisatorsystem enthält.6. Composition according to one of claims 1 to 5, characterized in that there are 5 wt .-% to 35 wt .-% water-soluble organic builder, up to 15 wt .-%, in particular 0.1 wt .-% to 5 wt % water-insoluble inorganic builder, up to 15% by weight, in particular 0.5% by weight to 10% by weight, synthetic anionic surfactant, 1% by weight to 40% by weight nonionic surfactant, up to 15 % By weight, in particular 4% by weight to 12% by weight of soap and up to 30% by weight, in particular 1% by weight to 25% by weight of water and / or water-miscible solvent and up to Contains 10 wt .-%, in particular 0.01 wt .-% to 7.5 wt .-% enzyme stabilizer system.
7. Mittel nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, daß das Glykosid der Formel (I) ein Alkyl- oder Alkenylglucosid ist und einen Oligomerisierungsgrad n unter 1,5, insbesondere 1,2 bis 1,4, besitzt.7. Composition according to one of claims 1 to 6, characterized in that the glycoside of formula (I) is an alkyl or alkenyl glucoside and has a degree of oligomerization n below 1.5, in particular 1.2 to 1.4.
8. Mittel nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß es Glykosid gemäß Formel (I) und Alkyl- beziehungsweise Alkeny- beziehungs¬ weise Ethersulfat mit einem linearen, primären Alkyl- beziehungsweise Alkenylrest mit 14 bis 18 C-Atomen im Gewichtsverhältnis 5:1 bis 1:4, insbesondere 1:1 bis 1:3,5 enthält. 8. Composition according to one of claims 1 to 7, characterized in that it contains glycoside according to formula (I) and alkyl or alkeny-, respectively, ether sulfate with a linear, primary alkyl or alkenyl radical having 14 to 18 carbon atoms in a weight ratio 5: 1 to 1: 4, in particular 1: 1 to 1: 3.5 contains.
EP95900124A 1993-11-18 1994-11-09 Liquid detergent and cleaner containing combinations of enzymes Expired - Lifetime EP0729502B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4339382A DE4339382A1 (en) 1993-11-18 1993-11-18 Liquid detergents and cleaning agents containing enzyme combinations
DE4339382 1993-11-18
PCT/EP1994/003691 WO1995014074A1 (en) 1993-11-18 1994-11-09 Liquid detergent and cleaner containing combinations of enzymes

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EP0729502A1 true EP0729502A1 (en) 1996-09-04
EP0729502B1 EP0729502B1 (en) 1999-07-28

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DE (2) DE4339382A1 (en)
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EP0798371A1 (en) * 1996-03-29 1997-10-01 The Procter & Gamble Company Detergent compositions comprising specific amylase and alkyl poly glucoside surfactants
EP1012219A1 (en) * 1997-07-11 2000-06-28 The Procter & Gamble Company Detergent compositions comprising a specific cellulase and an alkyl poly glucoside surfactant
BE1027322B1 (en) * 2019-05-29 2021-01-12 Realco Cleaning and degreasing composition for the treatment of hard surfaces

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WO1986005187A1 (en) * 1985-03-07 1986-09-12 A.E. Staley Manufacturing Company Detergent composition containing an enzyme and a glycoside surfactant
US4959179A (en) * 1989-01-30 1990-09-25 Lever Brothers Company Stabilized enzymes liquid detergent composition containing lipase and protease
GB8923788D0 (en) * 1989-10-23 1989-12-13 Unilever Plc Enzymatic detergent compositions and their use

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ES2136270T3 (en) 1999-11-16
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