WO2008000562A1 - Portion de détergent ou de produit traitant à gradient de solubilité et/ou de dispersibilité - Google Patents

Portion de détergent ou de produit traitant à gradient de solubilité et/ou de dispersibilité Download PDF

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Publication number
WO2008000562A1
WO2008000562A1 PCT/EP2007/054977 EP2007054977W WO2008000562A1 WO 2008000562 A1 WO2008000562 A1 WO 2008000562A1 EP 2007054977 W EP2007054977 W EP 2007054977W WO 2008000562 A1 WO2008000562 A1 WO 2008000562A1
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WO
WIPO (PCT)
Prior art keywords
washing
agent portion
treating agent
solubility
acid
Prior art date
Application number
PCT/EP2007/054977
Other languages
German (de)
English (en)
Inventor
Frank Meier
Matthias Sunder
Dieter Nickel
Katja Peveling
Original Assignee
Henkel Ag & Co. Kgaa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel Ag & Co. Kgaa filed Critical Henkel Ag & Co. Kgaa
Publication of WO2008000562A1 publication Critical patent/WO2008000562A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • C11D17/0065—Solid detergents containing builders
    • C11D17/0073—Tablets
    • C11D17/0078—Multilayered tablets
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/18—Hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3707—Polyethers, e.g. polyalkyleneoxides
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10—Objects to be cleaned
    • C11D2111/12—Soft surfaces, e.g. textile

Definitions

  • the present invention relates to a dimensionally stable detergent or treating agent portion having a mass of at least 50 g, a process for producing this washing or treating agent portion, a kit comprising the washing or treating agent portion and a bag or container, a process for washing and / or treating of textiles in an automatic washing machine in which the washing or treating agent portion or kit is used, and the use of the washing or treating agent portion or automatic dosing kit in the drum of an automatic washing machine for textiles.
  • Detergents or treatment agents are available today for the consumer in a variety of forms. In addition to powders and granules, this offer also includes, for example, concentrates in the form of extruded or tableted compositions. These fixed, concentrated or compressed forms of supply are characterized by a reduced volume per dosing unit and thus reduce the costs for packaging and transport. In particular, the washing or treatment tablets additionally meet the consumer's desire for simplified dosage. The corresponding means are comprehensively described in the prior art. However, in addition to the advantages listed, compacted detergents or treatment agents also have a number of disadvantages. Especially tableted supply forms are characterized by their high compression often by a delayed disintegration and thus a delayed release of their ingredients.
  • solid or liquid detergents or treatment agents which comprise a water-soluble or water-dispersible packaging have been increasingly described in recent years. have. These agents are characterized as the tablets by a simplified dosage, since they can be dosed together with the outer packaging in the washing machine, but on the other hand they also allow the preparation of liquid or powdered washing or treating agent, which compared to the compact data by a better Distinguish resolution and faster effectiveness.
  • the means mentioned so far have in common that the consumer must always dose the washing or treatment agent separately for each washing or treatment cycle.
  • the tablets, powders, granules, liquids, gels and solid and liquid washing or treating agents repackaged in individual portions are completely consumed in the particular washing or treatment cycle selected.
  • the object of the present invention was to overcome the disadvantages of the known detergents or treatment agents.
  • a washing or treating agent should be provided, which can be dosed more easily and which - regardless of the size of the remaining portion of detergent or treating agent - releases substantially the same amount of ingredients in comparable washing or treating operations in an automatic washing machine for textiles.
  • the present application is a dimensionally stable, one-piece washing or treating agent portion having a mass of at least 50 g, which has a solubility and / or dispersibility gradients.
  • solubility and / or dispersibility gradient it is preferable for the solubility and / or dispersibility gradient to be substantially from the center of the room to the surface of the washing or treating agent portion, ie "radially.” It is preferred that the solubility and / or dispersibility of the washing or treating agent portion be radially in the direction Surface decreases.
  • the term "solubility or dispersibility gradient” is understood as meaning both continuously extending gradients and also those gradients whose progress has jumps, that is to say that the washing or treatment agent portion is in the form of several active-agent-containing phases or active substance-containing (shell) Layers is present and these phases or layers have a different solubility and / or dispersibility.
  • the detergent or treating agent portion comprises pressed material having a radial density gradient.
  • the density of the compressed material preferably increases radially toward the surface.
  • the washing or treatment agent portion is composed of several layers which have different solubilities and / or dispersing capabilities.
  • the solubilities and / or dispersing capabilities of these layers preferably decrease radially towards the surface of the detergent or treating agent portion.
  • a washing or treating agent portion according to the invention is used in an automatic washing machine for textiles, it is preferred that essentially the same amount of the washing or treating agent portion is always dissolved or dispersed during the first use of the portion and the further applications of this portion in comparable washing or treatment operations.
  • the deviation is at a Application detached or dispersed amount of washing or treatment agent portion of the average of the detached or dispersed substance amounts always less than 30 wt .-%, preferably less than 20 wt .-%, more preferably less than 10 wt .-% and in particular less than 5% by weight.
  • the washing or treating agent portion preferably has a mass of from 75 to 1500 g, preferably from 100 to 1000 g, particularly preferably from 200 to 850 g and in particular from 300 to 700 g.
  • the washing or treating agent portion preferably has the form of a prism, preferably a cuboid or an ellipsoid, preferably a spheroid, in particular a flattened or prolapsed spheroid or a sphere.
  • the shape of the washing or treating agent portion corresponds to a prolapsed spheroid having the geometric characteristics of a rugby ball.
  • the washing or treating agent portion is spherical and thus has the shape of a ball.
  • the washing or treatment agent portion preferably releases over 2 to 60, more preferably over 4 to 50, and in particular more than 6 to 40 washing or treatment courses in an automatic washing machine for textiles active substance.
  • washing or treating agents in the form of powders, granules or tablets the requirement of rapid solubility / dispersibility or rapid disintegration is made.
  • the active substances of these agents should be available as early as possible at the beginning of the washing or treatment cycle for which they were dosed individually.
  • rapid disintegration is achieved, for example, by adding so-called tablet disintegrators.
  • the solubility / dispersibility is determined by knocking out a sample of defined mass from the detergent or treating agent portion of the invention or preparing a sample portion of the active-containing shell by compressing or casting the corresponding composition in a small mold and subjecting these samples to a standardized solubility test.
  • a defined amount of city water of the specified water hardness and the respective temperature is placed in a beaker and kept in motion by means of a laboratory stirrer with stirring blades.
  • the above-mentioned samples of defined amount are metered into the water and it is stirred for 300 seconds.
  • the solution through a sieve (mesh size 200 .mu.m) is cast glass beaker and agitator blades are rinsed with a minimum of cold water over the sieve, the sieve dried in a drying oven at 40 0 C to constant weight and by means of differential weighing the residue on the sieve.
  • the amount of dissolved / dispersed substance is calculated from the difference between the amount of sample used and the residue. At least one double determination is carried out.
  • alkaline earths determine the quality of the water for cleaning purposes.
  • Calcium and magnesium ions form sparingly soluble salts with soap, the lime soap and magnesium soap. It is also possible with other anionic surfactants to form sparingly soluble compounds.
  • sparingly soluble alkaline earth metal carbonates can deposit on the laundry and the heating rods of the washing machines. When washing alkaline earth ions are therefore generally undesirable.
  • the sum of alkaline earths is recorded in terms of water hardness (total hardness). It is called water with a high content of calcium and magnesium ions as hard, such low content as soft.
  • the figures are determined in terms of degrees of hardness.
  • the hardness of the water used is given in the unit German degree of hardness (° d) in use in Germany.
  • water of 1 ° d are 0.178 mmol / l Ca 2+ and Mg 2+ ions or water, which contains 1 mmol / l Ca 2+ and Mg 2+ ions, has a water hardness of 5.6 ° d .
  • a disturbing effect when washing show iron and iron ions, which occur in low concentration in drinking and surface water. They form sparingly soluble salts in aqueous solution which can be identified by their yellow to brown color.
  • the content of these salts in the city water used for the solubility test is preferably below 0.01 mg / 100 ml, in particular below 0.005 mg / 100 ml.
  • a reduced solubility / dispersibility compared to the laundry or treating agents which need to be dispensed separately per wash can be achieved in the detergent or treating agent portions of the present invention by compounding the washing or treating agent portion with a solubility control system.
  • the system for controlling the solubility is preferably in homogeneous admixture with the detergent or treating agent composition and thus controls the solubility or the dispersibility of the respective washing or treatment agent phase or layer.
  • the portion is preferably made up of several layers containing different systems for controlling the solubility and / or which are pressed to different extents, and which are preferably arranged in the portion in such a way in that the solubility / dispersibility of the individual layers decreases radially towards the surface.
  • the system for controlling the solubility of the washing or treating agent portion is preferably in an amount of at least 5 wt .-%, preferably of at least 10 wt .-%, particularly preferably from at least 15 wt .-%, most preferably in an amount of 20 to 65 wt .-% and in particular in an amount of 25 to 60 wt .-%.
  • the system for controlling the solubility preferably comprises at least one component which has a softening temperature between 35 and 200 ° C., preferably between 45 and 150 ° C.
  • solubility preferably comprises a component which possibilities at 15 ° C and 50 0 C significantly different solubility / dispersibilities in water (see above Illustrated solubility) has.
  • a component which possibilities at 15 ° C and 50 0 C significantly different solubility / dispersibilities in water (see above Illustrated solubility) has.
  • dissolve / disperse from this component in 15 ° C warm water (city water, 16 ° d) at most 20 wt .-%, preferably at most 10 wt .-% and in particular at most 5 wt .-% of the mass, which is otherwise identical conditions of the component in 50 0 C warm water (city water, 16 ° d) dissolves / dispersed.
  • all compounds which have a suitable solubility / dispersion profile can be present in the system for controlling the solubility.
  • Particularly suitable are compounds from the group of polymers, which can also be used in combination with one another.
  • Suitable polymers are a) water-soluble nonionic polymers from the group of a1) polyvinylpyrrolidones, a2) vinylpyrrolidone / vinyl ester copolymers, a3) cellulose ethers
  • Alkali and ammonium salts c2) Acrylamidoalkyltrialkylammonium chloride / methacrylic acid copolymers and their alkali metal and ammonium salts c3) Methacroylethylbetain / methacrylate copolymers
  • the solubility control system comprises one or more water-soluble polymer (s), preferably a material from the group (optionally acetalized) polyvinyl alcohol (PVAL), polyvinylpyrrolidone, polyethylene oxide, gelatin, cellulose and derivatives thereof and their mixtures.
  • PVAL polyvinyl alcohol
  • PVP polyvinylpyrrolidone
  • polyethylene oxide polyethylene oxide
  • gelatin cellulose and derivatives thereof and their mixtures.
  • the solubility controlling system at least partially comprises a polyvinyl alcohol whose degree of hydrolysis is 70 to 100 mol%, preferably 80 to 90 mol%, more preferably 81 to 89 mol%, and especially 82 to 88 mol%.
  • a polyvinyl alcohol whose degree of hydrolysis is 70 to 100 mol%, preferably 80 to 90 mol%, more preferably 81 to 89 mol%, and especially 82 to 88 mol%.
  • the degree of polymerization of such preferred polyvinyl alcohols is between about 200 to about 2100, preferably
  • the water solubility of PVAL can be altered by post-treatment with aldehydes (acetalization) or ketones (ketalization).
  • aldehydes acetalization
  • ketones ketalization
  • Polyvinyl alcohols which have been acetalated or ketalized with the aldehyde or keto groups of saccharides or polysaccharides or mixtures thereof have proven particularly advantageous.
  • reaction products of PVAL and starch are particularly advantageous.
  • PVP Polyvinylpyrrolidones
  • PVP are prepared by radical polymerization of 1-vinylpyrrolidone.
  • Commercially available PVP have molecular weights in the range of about 2,500 to 750,000 g / mol and are offered as white, hygroscopic powders or as aqueous solutions.
  • Polyethylene oxides, PEOX for short, are polyalkylene glycols of the general formula
  • ethylene oxide oxirane
  • ethylene glycol as the starting molecule. They have molar masses in the range of about 200 to 5,000,000 g / mol, corresponding to degrees of polymerization n of about 5 to> 100,000.
  • Polyethylene oxides have an extremely low concentration of reactive hydroxy end groups and show only weak glycol properties.
  • Gelatin is a polypeptide (molecular weight: about 15,000 to> 250,000 g / mol), which is obtained primarily by hydrolysis of the collagen contained in the skin and bones of animals under acidic or alkaline conditions.
  • the amino acid composition of gelatin is broadly similar to that of the collagen from which it was obtained and varies depending on its provenance.
  • the use of gelatin as water-soluble coating material is extremely widespread, especially in pharmacy in the form of hard or soft gelatin capsules. In the form of films, gelatin has little use because of its high price compared to the polymers mentioned above.
  • Preferred as a component of the solubility control system are materials comprising a polymer selected from the group consisting of starch and starch derivatives, cellulose and cellulose derivatives, in particular methyl cellulose, and mixtures thereof.
  • Starch is a homoglycan, wherein the glucose units are linked ⁇ -glycosidically.
  • Starch is composed of two components of different molecular weight; from about 20 to 30% straight-chain amylose (MW about 50,000 to 150,000) and 70 to 80% branched-chain amylopectin (MW about 300,000 to 2,000,000). In addition, small amounts of lipids, phosphoric acid and cations are still included.
  • amylose forms long, helical, entangled chains with about 300 to 1,200 glucose molecules as a result of the 1,4-position bond
  • the amylopectin branch branches off into a branch-like structure after an average of 25 glucose building blocks by 1,6-binding with about 1,500 to 12,000 molecules of glucose.
  • starch derivatives which are obtainable from starch by polymer-analogous reactions are also suitable.
  • Such chemically modified starches include, for example, products of esterifications or etherifications in which hydroxy hydrogen atoms have been substituted.
  • starches in which the hydroxy groups have been replaced by functional groups that are not bonded via an oxygen atom can also be used as starch derivatives.
  • the group of starch derivatives includes, for example, alkali starches, carboxymethyl starch (CMS), starch esters and ethers, and amino starches.
  • Pure cellulose has the formal gross composition (C 6 H 10 Os) n and is formally a ⁇ -1,4-polyacetal of cellobiose, which in turn is composed of two molecules of glucose.
  • Suitable celluloses consist of about 500 to 5,000 glucose units and therefore have average molecular weights of 50,000 to 500,000.
  • fusible substances from the group of fats and / or triglycerides and / or fatty acids and / or fatty alcohols and / or waxes and / or paraffins.
  • Fat (s) or triglyceride (s) is the name for compounds of glycerol in which the three hydroxy groups of glycerol are esterified by carboxylic acids.
  • the naturally occurring fats are triglycerides, which usually contain different fatty acids in the same glycerol molecule.
  • synthetic triglycerides in which only one fatty acid is bound are also available (for example tripalmitin, triolein or tristearin).
  • Natural and / or synthetic fats and / or mixtures of the two are preferred as a component of the solubility control system.
  • fatty acids in the present application aliphatic saturated or unsaturated, carboxylic acids with branched or unbranched carbon chain called.
  • carboxylic acids with branched or unbranched carbon chain called.
  • fatty acids a variety of manufacturing methods exist. While the lower fatty acids are mostly oxidative processes starting from alcohols and / or aldehydes As well as aliphatic or acyclic hydrocarbons based, the higher homologs most often still today most accessible by saponification of natural fats. With advances in transgenic plants, there are now almost limitless possibilities for varying the fatty acid spectrum in the storage fats of oil plants.
  • Preferred fatty acids in the context of the present invention have a melting point which permits processing of these fats in a casting process.
  • fatty acids have proved to be particularly advantageous, which have a melting point above 25 ° C.
  • Preferred components of the solubility control system are therefore capric acid and / or undecanoic acid and / or lauric acid and / or tridecanoic acid and / or myristic acid and / or pentadecanoic acid and / or palmitic acid and / or margaric acid and / or stearic acid and / or nonadecanoic acid and / or Arachinic acid and / or erucic acid and / or elaeosteraric acid.
  • fatty acids with a melting point below 25 ° C can be used.
  • Fatty alcohol is a collective name for the linear, saturated or unsaturated primary alcohols having 6 to 22 carbon atoms obtainable by reduction of the triglycerides, fatty acids or fatty acid esters.
  • the fatty alcohols may be saturated or unsaturated depending on the method of preparation.
  • the system for controlling the solubility in the washing or treating agent portions according to the invention contains waxes.
  • Preferred waxes have a melting range of between about 35 ° C and about 75 ° C. That is, in the present case, the melting range occurs within the specified temperature interval and does not indicate the width of the melting range. Waxes with such a melting range are dimensionally stable at room temperature, but melt at typical automatic washing machine temperatures of 30 0 C to 90 0 C and are therefore more easily water-dispersible at these temperatures.
  • Waxing is understood to mean a series of naturally or artificially produced substances which generally melt above 40 ° C. without decomposition and are already relatively low-viscous and non-stringy just above the melting point. They have a strong temperature-dependent consistency and solubility. According to their origin, the waxes are divided into three groups, the natural waxes, chemically modified waxes and the synthetic waxes.
  • the natural waxes include, for example, vegetable waxes such as candelilla wax, carnauba wax, Japan wax, Espartograswachs, cork wax, guaruma wax, rice germ oil wax, sugarcane wax, ouricury wax, or montan wax, animal waxes such as beeswax, shellac wax, spermaceti, lanolin (wool wax), or crepe fat, mineral waxes such as ceresin or ozokerite (groundwax), or petrochemical waxes such as petrolatum, paraffin waxes or microwaxes.
  • vegetable waxes such as candelilla wax, carnauba wax, Japan wax, Espartograswachs, cork wax, guaruma wax, rice germ oil wax, sugarcane wax, ouricury wax, or montan wax
  • animal waxes such as beeswax, shellac wax, spermaceti, lanolin (wool wax), or crepe
  • the chemically modified waxes include, for example, hard waxes such as montan ester waxes, Sassol waxes or hydrogenated jojoba waxes.
  • Synthetic waxes are generally understood as meaning polyalkylene waxes or polyalkylene glycol waxes. It is also possible to use as meltable or softenable substances for the compositions which cure by cooling, and compounds of other substance classes which fulfill the stated requirements with regard to the softening point. Suitable synthetic compounds, for example, higher esters of phthalic acid, in particular dicyclohexyl have hexyl phthalate, commercially available under the name Unimoll 66 ® (Bayer AG) is available, proven. Also suitable are synthetic waxes made of lower carboxylic acids and fatty alcohols, such as dimyristyl tartrate, sold under the name Cosmacol ® ETLP (Condea) is available.
  • esters of lower alcohols can be used with fatty acids from natural sources.
  • This class of substances includes, for example, Tegin® 90 (Goldschmidt), a glycerol monostearate palmitate.
  • Shellac for example shellac KPS-Dreiring-SP (Kalkhoff GmbH) can also be used.
  • Wax alcohols are higher molecular weight, water-insoluble fatty alcohols having generally about 22 to 40 carbon atoms.
  • the wax alcohols are, for example, in the form of wax esters of higher molecular weight fatty acids (wax acids) as the main constituent of many natural waxes.
  • wax alcohols are lignoceryl alcohol (1-tetracosanol), cetyl alcohol, myristyl alcohol or melissyl alcohol.
  • the coating of the present invention the solid particles coated can optionally also contain wool wax alcohols which are understood to be understood triterpenoid and steroid alcohols, for example lanolin, available, for example, under the trade designation Argowax ® (Pamentier & Co).
  • wool wax alcohols which are understood to be understood triterpenoid and steroid alcohols, for example lanolin, available, for example, under the trade designation Argowax ® (Pamentier & Co).
  • the solubility control system includes paraffin wax (paraffins).
  • paraffin wax preferably, at least 50% by weight of the system is for control the solubility of paraffin wax.
  • Particularly suitable are paraffin wax contents (based on the total weight of the system for controlling the solubility) of about 60 wt .-%, about 70 wt .-% or about 80 wt .-%, with even higher levels of, for example, more than 90 wt. % are particularly preferred.
  • the entire system for controlling solubility is paraffin wax.
  • paraffin waxes have the advantage over the other natural waxes mentioned that they do not undergo hydrolysis in an alkaline environment (as is to be expected, for example, with wax esters), since paraffin wax contains no hydrolyzable groups.
  • Paraffin waxes consist mainly of alkanes as well as low levels of iso- and cycloalkanes.
  • the content of the paraffin wax used at ambient temperature usually about 10 to about 30 0 C solid alkanes, isoalkanes and cycloalkanes as high as possible.
  • Preferred components for the system for controlling the solubility are also polyalkylene glycols, preferably polyethylene glycols and polypropylene glycols.
  • n can assume values between 1 (ethylene glycol) and several thousand.
  • n can assume values between 1 (ethylene glycol) and several thousand.
  • PEG average relative molecular weight
  • PEG 200 characterizes a polyethylene glycol having a relative molecular weight of about 190 to about 210.
  • the average relative molecular weight of the polyalkylene glycol (s) used is preferably between 200 and 36,000, preferably between 200 and 14,000 and particularly preferably between 300 and 12,000.
  • Polypropylene glycols are polymers of propylene glycol which are of the general formula
  • solubility control system which comprise a nonionic polymer, preferably a poly (alkylene) glycol, preferably a poly (ethylene) glycol and / or a poly (propylene) glycol, where the weight fraction of the poly (ethylene) glycol in the total weight of the solubility control system is preferably between 10 and 90% by weight, more preferably between 30 and 80% by weight and in particular between 50 and 70% by weight.
  • systems for controlling the solubility which are more than 92% by weight, preferably more than 94% by weight, more preferably more than 96% by weight, very preferably more than 98% by weight and in particular 100% %
  • poly (alkylene) glycol preferably poly (ethylene) glycol and / or poly (propylene) glycol, but in particular poly (ethylene) glycol.
  • Systems for controlling the solubility which in addition to poly (ethylene) glycol also contain poly (propylene) glycol, preferably have a ratio of the weight fractions of poly (ethylene) glycol to poly (propylene) glycol between 40: 1 and 1: 2, preferably between 20: 1 and 1: 1, more preferably between 10: 1 and 1, 5: 1 and in particular between 7: 1 and 2: 1.
  • nonionic surfactants which are used alone, but more preferably in combination with a nonionic polymer.
  • Detailed information on the usable nonionic surfactants can be found in the context of the description of washing or treatment-active substances.
  • Another class of compounds that is preferred for use in the solubility control system are the sugars, sugar acids, and sugar alcohols.
  • the monosaccharides, disaccharides and oligosaccharides and derivatives and mixtures thereof are preferably used. Particularly preferably glucose, fructose, ribonucleic se, maltose, lactose, sucrose, maltodextrin and isomalt are ® and mixtures of two, three, four or more mono- and / or di-saccharides and / or derivatives of mono- and / or di-saccharides ,
  • sugar acids can be used alone or in combination with other substances such as the above-mentioned sugars as part of a preferred liquid release agent.
  • Preferred sugar acids are gluconic acid, galactonic acid, mannonic acid, fructonic acid, arabinonic acid, xylonic acid, ribonic acid, and 2-deoxyribonic acid and derivatives thereof.
  • derivatives of the sugar acids, sugars and / or sugar derivatives or alone are used compounds from the group of the sugar alcohols, preferably mannitol, sorbitol, xylitol, dulcitol and arabitol.
  • Suitable polyhydric alcohols as components of the solubility control system are compounds having at least two hydroxyl groups. The physical state of these compounds at room temperature (20 0 C) is fixed.
  • Particularly suitable polyhydric alcohols are, for example, trimethylolpropane, pentaerythritol and the "sugar alcohols", ie the polyhydroxy compounds formed from monosaccharides by reduction of the carbonyl group.
  • sucrose alcohols ie the polyhydroxy compounds formed from monosaccharides by reduction of the carbonyl group.
  • particularly suitable sugar alcohols are, for. B. Threit u.
  • Erythritol Erythritol, adonite (ribitol), arabitol (formerly: lyxite) and xylitol, dulcitol (galactitol), mannitol and sorbitol (glucitol), the latter also being referred to as sorbitol.
  • polyurethanes are polyadducts of at least two different monomer types, a di- or polyisocyanate (A) and a compound (B) having at least 2 active hydrogen atoms per molecule.
  • the polyurethanes used as solution or suspension or dispersion are obtained from reaction mixtures in which at least one diisocyanate and at least one polyethylene glycol and / or at least one polypropylene glycol are present.
  • reaction mixtures may contain further polyisocyanates.
  • a content of the reaction mixtures - and thus of the polyurethanes - on other diols, triols, diamines, triamines, polyetherols and polyesterols is possible.
  • the compounds having more than 2 active hydrogen atoms are usually used only in small amounts in combination with a large excess of compounds having 2 active hydrogen atoms.
  • the polyurethanes contain diisocyanates as monomer unit.
  • the diisocyanates used are predominantly hexamethylene diisocyanate, 2,4- and 2,6-toluene diisocyanate, 4,4'-methylenedi (phenyl isocyanate) and in particular isophorone diisocyanate.
  • the polyurethanes furthermore contain diols as the monomer component, these diols originating at least partially from the group of the polyethylene glycols and / or the polypropylene glycols.
  • the polyurethanes have molecular weights of from 5,000 to 150,000 gmol -1 , preferably from 10,000 to 100,000 gmol -1, and more preferably from 20,000 to 50,000 gmol -1 .
  • the layers within the detergent or treating agent portion comprise pressed material and / or a system for controlling the solubility of the respective layer.
  • the system for controlling the solubility preferably comprises one or more components from the group of polyethylene glycols, polypropylene glycols, polybutyrates, polyhydric alcohols, sugars, polyurethanes, natural waxes, chemically modified waxes, synthetic waxes, wax alcohols, wax esters, paraffins, polyvinyl alcohols, polyacrylic acids and their derivatives, gelatin and celluloses.
  • Particularly preferred are solubility control systems comprising paraffins and / or polyethylene glycols.
  • suitable components of a system for controlling the solubility of the washing or treating agent portions according to the invention are amorphous silica and potassium silicate.
  • Layers of the detergent or treating agent portion containing a system for controlling the solubility of the respective layer are preferably obtained by lowering the temperature, incorporating water of hydration or other solvent components, reacting components contained in the fluid masses, modification conversions, evaporating water or other solvent components, condensation , Irradiated or solidified by pressing.
  • Particularly preferred detergent or treating agent portions comprise multiple layers containing as systems for controlling the solubility of the respective layer polyethylene glycol of different average molecular mass and / or paraffins of different average molecular mass.
  • the layers are preferably arranged such that the solubility and / or dispersibility of the washing or treatment agent portion decreases radially in the direction of the surface.
  • the washing or treating agent portion according to the invention has at least two, preferably between 3 and 20 and in particular 4 to 15 layers which, when used in an automatic washing machine, are dissolved / dispersed essentially successively, from outside to inside become. It is particularly preferred if, per washing or treatment cycle, at most one, preferably one of the layers of the washing or treating agent is consumed.
  • the individual layers of the detergent or treating agent portion contain substantially the same detergent or treating agent composition except for the solubility control system. If a layer of the portion is always dissolved / dispersed in several washing or treatment courses, the same active ingredients are preferably always released in the same quantitative ratio and preferably in a comparable amount. However, it can also be provided that the individual layers differ in composition. It is preferred, for example, that the layers have different colors, so that the consumer can understand the layer degradation on the basis of the color change of the washing or treatment agent portion. Also preferred is the packaging of the individual layers with different perfumes, which causes the textiles washed or treated in separate washing or treatment courses to have a different fragrance.
  • the washing or treating agent portion according to the invention comprises a base detergent for white and / or colored textiles, delicate textiles and / or wool.
  • Basic detergents for white textiles or colored textiles are known to consumers in Europe under the term heavy duty detergent or color washing medium.
  • Basic laundry detergents for wool are commercially available under the term wool detergents.
  • the term "basic detergents for delicate textiles" is intended to encompass all substances which are suitable for washing and treating special textiles Examples of such basic detergents are light detergents, curtain detergents, black textile detergents, white textile detergents , which should not be brought into contact with heavy-duty detergents, detergents for synthetic textiles etc. Suitable ingredients of basic detergents are listed later.
  • the portion preferably has a mass of from 150 to 1000 g, preferably from 250 to 900 g, more preferably from 300 to 800 g and in particular from 350 to 700 g.
  • the washing or treatment composition comprising a base detergent for white and / or colored textiles, sensitive textiles and / or wool contains significant amounts of surfactant, for example at least 6% by weight, preferably at least 9% by weight anionic surfactant.
  • a washing or treating agent portion of one of the above-mentioned base detergents so this preferably over 2 to 40, preferably over 4 to 30 and especially about 6 to 20 washing or treatment courses in an automatic washing machine for textiles free active.
  • wash cycle is understood to mean any wash program that can be set in an automatic washing machine, such as, for example, kitchen linen, coloreds, delicates, handwashes, wool washing programs at different temperatures.
  • treatment includes those programs of an automatic washing machine whose main focus is not on the cleaning of textiles, but their equipment and treatment. Examples of treatment courses are starches, rinsing, dyeing, soaking, etc .. Washing or treatment operations each include the actual washing or treatment cycles and rinsing cycles.
  • Per wash or treatment preferably 40 to 150 g, preferably 50 to 140 g, more preferably in particular 60 to 130 g and in particular 70 to 120 g of the base detergent-containing detergent or treatment agent portion dissolved / dispersed.
  • a preferred subject matter of the present invention is a dimensionally stable, one-part washing or treating agent portion having a mass of at least 50 g, comprising a base detergent for white and / or colored textiles, sensitive textiles and / or wool, which enzyme and / or substantial amounts of surfactant, preferably at least 6 wt .-% surfactant and having a solubility and / or dispersibility gradients.
  • the detergent or treatment agent portion comprises an additional component for a base detergent for white and / or colored textiles, sensitive textiles and / or wool, preferably a bleach, enzyme or finishing component for textiles, antimicrobial agents and / or nonionic surfactants, enzymes and mixtures of these components.
  • finishing components for textiles includes those components which are applied to the fibers of the textiles and thus bring about a change in the properties of the textile surfaces
  • suitable finishing components are fabric softening compounds such as cationic surfactants, clays, cationic polymers and polysiloxanes
  • Soil repellent polymers preferably from the group of terephthalic compounds, which are particularly preferably sulfonated, repellents or impregnating agents, antistatic agents, optical brighteners, UV protectants, skin care components and compounds such as silicone derivatives, which are an improvement
  • the textiles finishing components also include fragrance compositions, crease inhibitors, grayness inhibitors, shrinkage inhibitors, etc., as well as perfume compositions, wrinkle retardants, graying inhibitors, anti-wetting properties of the treated textiles, and ease of ironing the treated textiles der, fluorescers and color transfer inhibitors.
  • a washing or treating agent portion according to the invention comprising an additional component for a base detergent preferably has a mass of from 65 to 1000 g, preferably from 75 to 800 g, more preferably from 85 to 600 g and in particular from 95 to 500 g.
  • a washing or treating agent portion which comprises an additional component for a washing or treating agent, at least 20 wt .-%, preferably at least 30 wt .-% and in particular at least 40 wt .-% bleaching agent, at least 0.5 wt .-%, preferably at least 1, 5 wt .-% and in particular at least 2.5 wt .-% enzyme, at least 20 wt .-%, preferably at least 30 wt .-% and in particular at least 40 wt .-% of a plasticizer and / or at least 1, 5 wt .-%, preferably at least 3 wt .-%, particularly preferably at least 4.5 wt .-% and in particular at least
  • the washing or treating agent portion comprises an additional component
  • it preferably releases active substance in an automatic washing machine for from 5 to 60, preferably from 10 to 50 and in particular from 15 to 40 washing or treatment courses.
  • 1 to 60 g, preferably 1, 5 to 55 g and in particular 2 to 50 g of the additional component-containing washing or treatment agent portion are dissolved / dispersed per wash or treatment cycle.
  • Another preferred subject matter of the present invention is a dimensionally stable, one-part washing or treating agent portion having a mass of at least 50 g, comprising an additional component for a washing or treating agent, preferably a bleaching, enzyme and / or finishing component for textiles and at least 6 wt % Surfactant and a solubility or dispersibility gradient.
  • the detergent or treating agent portion contains equipment components as defined above, then it may be preferred that the active ingredients should be released primarily in the rinse cycles of a laundry or treat cycle.
  • the solubility / dispersibility of such agents is preferably controlled via the pH and / or ionic strength of the use liquor by means of a (physico) chemical switch so that the detergent or treating agent portion comprising the equipment component and the (physicochemical switch in the Cycles in which no or little washing or treating agents are dissolved in the water, ie in the rinsing cycles, dissolves / dispersed, however, in the cycles in which washing or treating agent is dissolved in a significant amount in the water, not or only to a small extent part dissolves / dispersed.
  • the active- material coating layer containing an inventive washing or treatment agent portion which has a gear component, in a 0.1 M sodium hydroxide (NaOH + city water 16 ° d, 20 0 C) and / or 1 M saline (saline + city water 16 ° d, 20 °) less than 30% by weight, preferably less than 25% by weight. , preferably less than 20 wt .-% and in particular less than 15 wt .-% of the mass, which under otherwise identical conditions by the coating layer containing the active ingredient in water (city water 16 ° d, 20 0 C, without further additives) dissolved / dispersed.
  • a gear component in a 0.1 M sodium hydroxide (NaOH + city water 16 ° d, 20 0 C) and / or 1 M saline (saline + city water 16 ° d, 20 °) less than 30% by weight, preferably less than 25% by weight.
  • saline saline + city water 16
  • the (physico-) chemical switch comprises one or more component (s) undergoing a change in the physical and / or chemical properties of a change in the electrolyte concentration (the ionic strength) in the washing, treatment or rinsing liquor .
  • the (physicochemical) chemical switch may include one or more components that change when the H + ion concentration (pH) in the wash, treatment or rinse liquor is changed the physical and / or chemical properties learns / experienced.
  • the (physico-) chemical switch causes the washing or treating agent in water, which has a high pH and / or a high ionic strength, a lower solubility / dispersibility, as in water, which has a lower pH Value and / or a lower ionic strength.
  • the (physico-) chemical switch itself has washing, treatment or rinse-active properties.
  • the (physicochemical switch preferably contains one or more substances from the group comprising (acidic) cellulose derivatives, in particular cellulose acetate phthalate, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose acetate succinate, methylcellulose, hydroxymethylcellulose, hydroxypropylcellulose, methylhydroxyethylcellulose, carboxymethylcellulose with different degrees of substitution, (acidic) poly (meth) ) acrylates, in particular methacrylic acid-methacrylate copolymer, methacrylic acid-ethyl acrylate copolymer, (acidic) polymers based on vinyl alcohol, in particular polyvinyl acetate phthalate, polyvinylpyrrolidones, polystyrene sulfonate, shellac, proteins, basic polymers and / or copolymers, in particular amino groups or aminoalkyl groups, imino groups and / or pyridine groups-containing basic polymers and / or copolymers and in particular aminoalky
  • Preferred constituents of the washing or treating agent portion are builders, nonionic surfactants, anionic surfactants, polymers, complexing agents, bleaching agents, bleach activators, bleach catalysts, enzymes, fragrances, dyes, pH adjusters, foam inhibitors, anti-settling agents or soil repellent polymers, grayness inhibitors, fabric softeners - Components, repellents or impregnating agents and antistatic agents, silicones, UV protection substances and optical brighteners. These are described below.
  • the builders include, in particular, the zeolites, silicates, carbonates, organic cobuilders and, where there are no ecological prejudices against their use, also the phosphates.
  • crystalline layered silicates of general formula NaMSi x O 2x + I ⁇ y H 2 O wherein M is sodium or hydrogen, x is a number from 1, 9 to 22, preferably from 1: 9 to 4, wherein particularly preferred Values for x are 2, 3 or 4, and y is a number from 0 to 33, preferably from 0 to 20.
  • the crystalline layered silicates of the formula NaMSi x O 2x + 1 ⁇ y H 2 O are sold for example by Clariant GmbH (Germany) under the trade name Na-SKS.
  • silicates Na-SKS-1 (Na 2 Si 22 O 45 .xH 2 O, kenyaite), Na-SKS-2 (Na 2 Sh 4 O 29 .xH 2 O, magadiite), Na-SKS -3 (Na 2 Si 8 Oi 7 .xH 2 O) or Na-SKS-4 (Na 2 Si 4 O 9 .xH 2 O, makatite).
  • crystalline layer silicates with the formula NaMSi x O 2x + 1 ⁇ y H 2 O, in which x stands for 2 h.
  • x stands for 2 h.
  • both .beta.- and ⁇ -sodium Na 2 Si 2 O 5 ⁇ y H 2 O and further in particular Na-SKS-5 ((X-Na 2 Si 2 O 5), Na SKS-7 (B- Na 2 Si 2 O 5, natrosilite), Na-SKS-9 (NaHSi 2 O 5 ⁇ H 2 O), Na-SKS-10 (NaHSi 2 O 5 ⁇ 3 H 2 O, kanemite), Na-SKS-11 (T-Na 2 Si 2 0 5 ) and Na-SKS-13 (NaHSi 2 O 5 ), but especially Na-SKS-6 (6-Na 2 Si 2 O 5 ) is preferred.
  • amorphous sodium silicates with a Na 2 O: SiO 2 modulus of from 1: 2 to 1: 3.3, preferably from 1: 2 to 1: 2.8 and in particular from 1: 2 to 1: 2.6, which preferably delayed release and have secondary washing properties.
  • the dissolution delay compared with conventional amorphous sodium silicates may have been caused in various ways, for example by surface treatment, compounding, compaction / densification or by overdrying.
  • a-morph is understood to mean that the silicates in X-ray diffraction experiments do not give sharp X-ray reflections typical of crystalline substances, but at most one or more maxima of the scattered X-rays having a width of several degrees of the diffraction angle.
  • X-ray amorphous silicates are used whose silicate particles produce blurred or even sharp diffraction maxima in electron diffraction experiments. This is to be interpreted as meaning that the products have microcrystalline regions of the size of ten to a few hundred nm, with values of up to max. 50 nm and in particular up to max. 20 nm are preferred.
  • Such X-ray amorphous silicates also have a dissolution delay compared to the conventional water glasses.
  • Particularly preferred are compacted / compacted amorphous silicates, compounded amorphous silicates and overdried X-ray amorphous silicates.
  • the alkali metal phosphates are the most important in the detergent and cleaner industry.
  • Alkalimetallphosphate is the summary term for the alkali metal (especially sodium and potassium) salts of various phosphoric acids, in which one can distinguish metaphosphoric acids (HPO 3 ) n and orthophosphoric H 3 PO 4 in addition to high molecular weight representatives.
  • the phosphates combine several advantages: they act as alkali carriers, prevent lime deposits on machine parts or lime incrustations in fabrics and also contribute to the cleaning performance.
  • phosphates are the pentasodium triphosphate, Na 5 P 3 O 10 (sodium tripolyphosphate) and the corresponding potassium salt pentapotassium triphosphate, K 5 P 3 Oi 0 (potassium tripolyphosphate).
  • the sodium potassium tripolyphosphates are also preferably used according to the invention.
  • alkali carriers are alkali metal hydroxides, alkali metal carbonates, alkali metal hydrogencarbonates, alkali metal sesquicarbonates, the alkali metal silicates, alkali metal silicates and mixtures of the abovementioned substances, preference being given to using alkali metal carbonates, in particular sodium carbonate, sodium bicarbonate or sodium sesquicarbonate for the purposes of this invention.
  • alkali metal carbonates in particular sodium carbonate, sodium bicarbonate or sodium sesquicarbonate for the purposes of this invention.
  • a builder system comprising a mixture of tripolyphosphate and sodium carbonate.
  • a builder system comprising a mixture of tripolyphosphate and sodium carbonate and sodium disilicate.
  • organic co-builders are polycarboxylates / polycarboxylic acids, polymeric polycarboxylates, aspartic acid, polyacetals, dextrins, further organic cobuilders (see below) and phosphonates. These classes of substances are described below.
  • Useful organic builders are, for example, the polycarboxylic acids which can be used in the form of the free acid and / or their sodium salts, polycarboxylic acids meaning those carboxylic acids which carry more than one acid function.
  • NTA nitrilotriacetic acid
  • the free acids also typically have the property of an acidifying component and thus also serve to set a lower and milder pH of detergents or cleaners.
  • citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any desired mixtures of these can be mentioned here.
  • polymeric polycarboxylates for example the alkali metal salts of polyacrylic acid or of polymethacrylic acid, for example those having a relative molecular mass of from 500 to 70,000 g / mol.
  • the molecular weights stated for polymeric polycarboxylates are weight-average molar masses M w of the particular acid form, which were determined in principle by means of gel permeation chromatography (GPC), a UV detector being used. The measurement was carried out against an external polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship with the polymers investigated. These data differ significantly from the molecular weight data, in which polystyrene sulfonic acids are used as standard. The molar masses measured against polystyrenesulfonic acids are generally significantly higher than the molecular weights specified in this document.
  • Suitable polymers are, in particular, polyacrylates which preferably have a molecular weight of 2,000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates, which have molar masses of from 2000 to 10000 g / mol, and particularly preferably from 3000 to 5000 g / mol, may again be preferred from this group.
  • copolymeric polycarboxylates in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid.
  • Copolymers of acrylic acid with maleic acid which contain 50 to 90% by weight of acrylic acid and 50 to 10% by weight of maleic acid have proven to be particularly suitable.
  • Their relative molecular weight, based on free acids is generally from 2000 to 70000 g / mol, preferably from 20,000 to 50,000 g / mol and in particular from 30,000 to 40,000 g / mol.
  • the polymers may also contain allylsulfonic acids such as allyloxybenzenesulfonic acid and methallylsulfonic acid as a monomer.
  • biodegradable polymers of more than two different monomer units for example those which contain as monomers salts of acrylic acid and maleic acid and vinyl alcohol or vinyl alcohol derivatives or as monomers salts of acrylic acid and 2-alkylallylsulfonic acid and sugar derivatives ,
  • copolymers are those which have as their monomers acrolein and acrylic acid / acrylic acid salts or acrolein and vinyl acetate.
  • polymeric aminodicarboxylic acids their salts or their precursors. Particular preference is given to polyaspartic acids or their salts.
  • polyacetals which can be obtained by reacting dialdehydes with polyolcarboxylic acids which have 5 to 7 C atoms and at least 3 hydroxyl groups.
  • Preferred polyacetals are obtained from dialdehydes such as glycolysis, glutaraldehyde, terephthalaldehyde and mixtures thereof and from polyol carboxylic acids such as gluconic acid and / or glucoheptonic acid.
  • dextrins for example oligomers or polymers of carbohydrates, which can be obtained by partial hydrolysis of starches.
  • the hydrolysis can be carried out by customary, for example acid or enzyme catalyzed processes.
  • it is hydrolysis products having average molecular weights in the range of 400 to 500,000 g / mol.
  • a polysaccharide with a dextrose equivalent (DE) in the range from 0.5 to 40, in particular from 2 to 30 is preferred, DE being a common measure of the reducing action of a polysaccharide compared to dextrose, which has a DE of 100 , is.
  • DE dextrose equivalent
  • oxidized derivatives of such dextrins are their reaction products with oxidizing agents which are capable of oxidizing at least one alcohol function of the saccharide ring to the carboxylic acid function.
  • Ethylenediamine-N, N'-disuccinate is preferably used in form of its sodium or magnesium salts.
  • glycerol disuccinates and glycerol trisuccinates are also preferred in this context.
  • organic cobuilders are, for example, acetylated hydroxycarboxylic acids or their salts, which may optionally also be present in lactone form and which contain at least 4 carbon atoms and at least one hydroxyl group and a maximum of two acid groups.
  • the washing or treating agent portion preferably comprises surfactants from the group of nonionic surfactants, anionic surfactants, amphoteric surfactants and / or zwitterionic surfactants, preferably nonionic and / or anionic surfactants.
  • the washing or treating agent portion preferably contains at least 6% by weight of surfactant, more preferably at least 8% by weight of surfactant, most preferably at least 10% by weight and in particular at least 12% by weight of surfactant.
  • nonionic surfactants it is possible to use all nonionic surfactants known to the person skilled in the art. Low-foaming nonionic surfactants are used as preferred surfactants. With particular preference, washing or treating agents contain nonionic surfactants from the group of alkoxylated alcohols.
  • the nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and an average of 1 to 12 moles of ethylene oxide (EO) per mole of alcohol in which the alcohol residue is linear or preferably methyl-branched in the 2-position may be or contain linear and methyl-branched radicals in the mixture, as they are usually present in Oxoalkoholresten.
  • EO ethylene oxide
  • alcohol ethoxylates with linear radicals of alcohols of natural origin having 12 to 18 carbon atoms, for example from coconut, palm, Taigfetto- or oleyl alcohol, and on average 2 to 8 moles of EO per mole of alcohol are preferred.
  • the preferred ethoxylated alcohols include, for example, C 12 -i 4 -alcohols with 3 EO or 4 EO, C 9 .
  • n-Alcohol with 7 EO Ci 3- i 5 alcohols with 3 EO, 5 EO, 7 EO or 8 EO, Ci 2 -i 8 -alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures from C 12 -i 4 -alcohol with 3 EO and C 12 _ 18 -alcohol with 5 EO.
  • the stated degrees of ethoxylation represent statistical averages, which may correspond to a particular product of an integer or a fractional number.
  • Preferred alcohol ethoxylates have a narrow homolog distribution (narrow rank ethoxylates, NRE).
  • NRE narrow rank ethoxylates
  • these nonionic surfactants fatty alcohols with more than 12 EO can also be used. Examples of these are tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.
  • nonionic surfactants and alkyl glycosides of the general formula RO (G) x can be used in which R is a primary straight-chain or methyl-branched, especially methyl-branched in the 2-position aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol which represents a glycose unit having 5 or 6 C atoms, preferably glucose.
  • the degree of oligomerization x which indicates the distribution of monoglycosides and oligoglycosides, is any number between 1 and 10; preferably x is 1, 2 to 1, 4.
  • nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably having from 1 to 4 carbon atoms in the alkyl chain.
  • Nonionic surfactants of the amine oxide type for example N-cocoalkyl-N, N-dimethylamine oxide and N-tallowalkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides may also be suitable.
  • the amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, especially not more than half thereof.
  • surfactants are polyhydroxy fatty acid amides of the formula
  • R is an aliphatic acyl radical having 6 to 22 carbon atoms
  • R 1 is hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms
  • [Z] is a linear or branched polyhydroxyalkyl radical having 3 to 10 carbon atoms and 3 to 10 hydroxyl groups.
  • the polyhydroxy fatty acid amides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.
  • the group of polyhydroxy fatty acid amides also includes compounds of the formula
  • R is a linear or branched alkyl or alkenyl radical having 7 to 12 carbon atoms
  • R 1 is a linear, branched or cyclic alkyl radical or an aryl radical having 2 to 8 carbon atoms
  • R 2 is a linear, branched or cyclic alkyl radical or an aryl radical or an oxyalkyl radical having from 1 to 8 carbon atoms
  • 4- alkyl or phenyl radicals are preferred
  • [Z] is a linear polyhydroxyalkyl radical whose alkyl chain is substituted by at least two hydroxyl groups, or alkoxylated, preferably ethoxylated or propoxylated derivatives of this radical.
  • [Z] is preferably obtained by reductive amination of a reduced sugar, for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • a reduced sugar for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • the N-alkoxy- or N-aryloxy-substituted compounds can be converted into the desired polyhydroxy fatty acid amides by reaction with fatty acid methyl esters in the presence of an alkoxide as catalyst.
  • Nonionic surfactants from the group of alkoxylated alcohols particularly preferably from the group of mixed alkoxylated alcohols and in particular from the group of EO / AO / EO nonionic surfactants, or the PO / AO / PO nonionic surfactants, especially the PO / EO / PO nonionic surfactants are particularly preferred.
  • Such PO / EO / PO nonionic surfactants are characterized by good foam control.
  • anionic surfactants for example, those of the sulfonate type and sulfates are used.
  • Suitable surfactants of the sulfonate type are preferably C 9 -i 3 -alkylbenzenesulfonates, olefinsulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and also disulfonates, as are known for example from C 1 2-18 monoolefins with terminal or internal double bond by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation products into consideration.
  • alkanesulfonates which are obtained from C 12-i 8 alkanes, for example by sulfochlorination or sulfoxidation and subsequent hydrolysis or neutralization.
  • esters of ⁇ -sulfo fatty acids esters of ⁇ -sulfo fatty acids (ester sulfonates), for example the ⁇ -sulfonated methyl esters of hydrogenated coconut, palm kernel or tallow fatty acids.
  • anionic surfactants are sulfated fatty acid glycerol esters.
  • Fatty acid glycerol esters are the mono-, di- and triesters and mixtures thereof, as obtained in the preparation by esterification of a monoglycerol with 1 to 3 moles of fatty acid or in the transesterification of triglycerides with 0.3 to 2 moles of glycerol become.
  • Preferred sulfated fatty acid glycerol esters are the sulfonation products of saturated fatty acids having 6 to 22 carbon atoms, for example caproic acid, caprylic acid, capric acid, myristic acid, lauric acid, palmitic acid, stearic acid or behenic acid.
  • Suitable alk (en) ylsulfates are the alkali metal salts and in particular the sodium salts of the sulfuric monoesters of C 12 -C 18 fatty alcohols, for example coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or the C 10 -C 2 o-oxo alcohols and those half-esters of secondary alcohols of these chain lengths are preferred.
  • alk (en) ylsulfates of said chain length which contain a synthetic, produced on a petrochemical basis straight-chain alkyl radical, which have an analogous degradation behavior as the adequate compounds based on oleochemical raw materials.
  • C 12 -C 16 alkyl sulfates and C 12 -C 15 alkyl sulfates and C 14 -C 15 alkyl sulfates are preferred.
  • 2,3-alkyl sulfates which can be obtained as commercial products from Shell Oil Company under the name DAN ®, are suitable anionic surfactants.
  • sulfuric acid monoesters of straight-chain or branched C 7 ethoxylated with 1 to 6 moles of ethylene oxide are suitable.
  • 2 i-alcohols such as 2-methyl-branched Cg.- ⁇ -alcohols having on average 3.5 mol of ethylene oxide (EO) or Ci 2 _i 8 -Fettalkohole with 1 to 4 EO, are suitable.
  • Suitable anionic surfactants are also the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic acid esters and which are monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • alcohols preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • Preferred sulfosuccinates contain C 8- 8 i - fatty alcohol radicals or mixtures thereof.
  • Particularly preferred sulfosuccinates contain a fatty alcohol residue derived from ethoxylated fatty alcohols, which by themselves are nonionic surfactants.
  • Sulfosuccinates whose fatty alcohol residues are derived from ethoxylated fatty alcohols with a narrow homolog distribution, are again particularly preferred.
  • alk (en) ylsuccinic acid having preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.
  • anionic surfactants are particularly soaps into consideration. Suitable are saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid and, in particular, soap mixtures derived from natural fatty acids, for example coconut, palm kernel or tallow fatty acids.
  • the anionic surfactants, including the soaps may be present in the form of their sodium, potassium or ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • the anionic surfactants are preferably present in the form of their sodium or potassium salts, in particular in the form of the sodium salts.
  • the group of polymers includes, in particular, the washing or treatment-active polymers and / or polymers which act as softeners.
  • cationic, anionic and amphoteric polymers can be used in detergents or treatment agents in addition to nonionic polymers.
  • “Cationic polymers” in the meaning of the present invention are polymers which carry a positive charge in the polymer molecule, which can be realized, for example, by (alkyl) ammonium groups or other positively charged groups present in the polymer chain quaternized cellulose derivatives, the polysiloxanes with quaternary groups, the cationic guar derivatives, the polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid, the copolymers of vinylpyrrolidone with quaternized derivatives of dialkylamino acrylate and methacrylate, the Vinylpyrrolidone-methoimidazolinium chloride copolymers, the quaternized polyvinyl alcohols or the polymers specified under the INCI names Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and Polyquaternium 27.
  • amphoteric polymers also have, in addition to a positively charged group in the polymer chain, also negatively charged groups or monomer units. These groups may, for example, be carboxylic acids, sulfonic acids or phosphonic acids.
  • the bleaching agents are a particularly preferred washing or treatment-active substance.
  • sodium percarbonate, sodium perborate tetrahydrate and sodium perborate hydrate have special meaning.
  • Other useful bleaching agents are, for example, peroxypyrrophosphates, citrate perhydrates and H 2 O 2 -forming peracidic salts or peracids, such as perbenzoates, peroxophthalates, diperazelaic acid, phthaloiminoperacid or diperdodecanedioic acid.
  • bleaching agents from the group of organic bleaching agents can also be used.
  • Typical organic bleaches are the diacyl peroxides such as dibenzoyl peroxide.
  • peroxyacids examples of which include the alkyl peroxyacids and the aryl peroxyacids.
  • Preferred representatives are (a) the peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, a- also peroxy- ⁇ -naphthoic acid and magnesium monoperphthalate, (b) the aliphatic or substituted aliphatic peroxyacids, such as peroxylauric acid, peroxystearic acid, ⁇ -phthalimidoperacycaproic acid [Phthaliminoperoxyhexanoic acid (PAP)], o-carboxybenzamidoperoxycaproic acid, N-nonylamidoperoperadipic acid and N-nonenylamidopersuccinates and (c) aliphatic and araliphatic peroxydicarboxylic acids, such as 1,12-diperoxycarboxylic acid, 1,9-
  • chlorine or bromine releasing substances can be used.
  • suitable chlorine or bromine releasing materials are, for example, heterocyclic N-bromo- and N-chloroamides, for example trichloroisocyanuric acid, tribromoisocyanuric acid, dibromoisocyanuric acid and / or dichloroisocyanuric acid (DICA) and / or their salts with cations such as potassium and sodium.
  • DICA dichloroisocyanuric acid
  • Hydantoin compounds such as 1,3-dichloro-5,5-dimethylhydantoin are also suitable.
  • Bleach activators are used in detergents or treating agents, for example, to achieve an improved bleaching effect at temperatures of 60 ° C. and below.
  • As bleach activators it is possible to use compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups.
  • polyacylated alkylenediamines in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylglycoluril (TAGU), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate and 2, 5-diacetoxy-2,5-dihydrofuran, n-methyl-morpholinium
  • Hydrophilic substituted acyl acetals and acyl lactams are also preferably used.
  • Combinations of conventional bleach activators can also be used.
  • Further bleach activators which are preferably used in the context of the present invention are compounds from the group of cationic nitriles, in particular cationic nitriles of the formula
  • R 1 is -H, -CH 3, a C 2 - 24 alkyl or alkenyl group, a substituted C 2-24 -alkyl or -alkenyl radical having at least one substituent from the group -Cl, -Br, - OH, -NH 2 , -CN, an alkyl or Alkenylarylrest with a C- ⁇ _ 24 alkyl group, or represents a substituted alkyl or Alkenylarylrest with a Ci_ 24 alkyl group and at least one further substituent on the aromatic ring
  • R 2 and R 3 are independently selected from -CH 2 -CN, -CH 3 , -CH 2 -CH 3 , -CH 2 -CH 2 -CH 3 , -CH (CH 3 ) -CH 3 , -CH 2 -OH, -CH 2 -CH 2 -OH, -CH (OH) -CH 3, -CH 2 - CH 2 -CH 2 -OH,
  • bleach catalysts can also be used.
  • These substances are bleach-enhancing transition metal salts or transition metal complexes such as, for example, Mn, Fe, Co, Ru or Mo saline complexes or carbonyl complexes.
  • Mn, Fe, Co, Ru, Mo, Ti, V and Cu complexes with N-containing tripod ligands and Co, Fe, Cu and Ru ammine complexes can also be used as bleach catalysts.
  • Bleach-enhancing transition metal complexes in particular having the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, preferably selected from the group of the manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (ammine) Complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes, the chlorides of cobalt or manganese, of manganese sulfate are used in conventional amounts.
  • complexes of manganese in the oxidation state II, IM, IV or IV which preferably contain one or more macrocyclic ligand (s) with the donor functions N, NR, PR, O and / or S.
  • ligands are used which have nitrogen donor functions.
  • bleach catalyst (s) in the compositions of the invention, which as macromolecular ligands 1, 4,7-trimethyl-1, 4,7-triazacyclononan (Me-TACN), 1, 4,7-triazacyclononane (TACN ), 1, 5,9-trimethyl-1, 5,9-triazacyclododecane (Me-TACD), 2-methyl-1, 4,7-trimethyl-1, 4,7-triazacyclononane (Me / Me-TACN) and or 2-methyl-1,4,7-triazacyclononane (Me / TACN).
  • macromolecular ligands 1, 4,7-trimethyl-1, 4,7-triazacyclononan (Me-TACN), 1, 4,7-triazacyclononane (TACN ), 1, 5,9-trimethyl-1, 5,9-triazacyclododecane (Me-TACD), 2-methyl-1, 4,7-trimethyl-1, 4,7-triazacyclononane (Me / Me-TACN)
  • Suitable manganese complexes are, for example, [Mn 1 " 2 ( ⁇ -O) 1 ( ⁇ -OAc) 2 (TACN) 2 ] (CIO 4 ) 2, [Mn" 1 Mn lv ( ⁇ -O) 2 ( ⁇ -)
  • Enzymes can be used to increase the washing performance of detergents or treatment agents. These include in particular proteases, amylases, lipases, hemicellulases, cellulases or oxidoreductases, and preferably mixtures thereof. These enzymes are basically of natural origin; Starting from the natural molecules, improved variants are available for use in detergents or treatment agents, which are preferably used accordingly.
  • subtilisins those of the subtilisin type are preferable.
  • subtilisins BPN 'and Carlsberg and their further developed forms the protease PB92, the subtilisins 147 and 309, the alkaline protease from Bacillus lentus, subtilisin DY and the subtilases, but not the subtilisins in the enzymes, thermase, proteinase K and the proteases TW3 and TW7.
  • amylases examples include the ⁇ -amylases from Bacillus licheniformis, from B. amyloliquefaciens, from B. stearothermophilus, from Aspergillus niger and A. oryzae, as well as the further developments of the aforementioned amylases which are improved for use in detergents or treating agents. Furthermore, for this purpose, the ⁇ -amylase from Bacillus sp. A 7-7 (DSM 12368) and the cyclodextrin glucanotransferase (CGTase) from B. agaradherens (DSM 9948).
  • lipases or cutinases in particular because of their triglyceride-splitting activities, but also in order to generate in situ peracids from suitable precursors.
  • suitable precursors include, for example, the lipases originally obtainable from Humicola lanuginosa (Thermomyces lanu- ginosus) or further developed, in particular those with the amino acid exchange D96L.
  • the cutinases can be used, originally isolated from Fusarium solani pisi and Humicola insolens. It is also possible to use lipases, or cutinases, whose initial enzymes were originally isolated from Pseudomonas mendocina and Fusarium solanii.
  • Oxidoreductases for example oxidases, oxygenases, catalases, peroxidases, such as halo, chloro, bromo, lignin, glucose or manganese peroxidases, dioxygenases or laccases (phenol oxidases, polyphenol oxidases) can be used to increase the bleaching effect.
  • peroxidases such as halo, chloro, bromo, lignin, glucose or manganese peroxidases, dioxygenases or laccases
  • phenol oxidases, polyphenol oxidases can be used to increase the bleaching effect.
  • organic, particularly preferably aromatic, compounds which interact with the enzymes in order to enhance the activity of the relevant oxidoreductases (enhancers) or to ensure the flow of electrons (mediators) at greatly varying redox potentials between the oxidizing enzymes and the soils.
  • the enzymes can be used in any form known in the art. These include, for example, the solid preparations obtained by granulation, extrusion or lyophilization or, especially in the case of liquid or gel-form detergents, solutions of the enzymes, advantageously as concentrated as possible, sparing in water and / or added with stabilizers.
  • the enzymes may be encapsulated for both the solid and liquid dosage forms, for example by spray-drying or extruding the enzyme solution together with a preferably natural polymer or in the form of capsules, for example those in which the enzymes are entrapped as in a solidified gel or in those of the core-shell type, in which an enzyme-containing core is coated with a water, air and / or chemical impermeable protective layer.
  • additional active ingredients for example stabilizers, emulsifiers, pigments, bleach or dyes may additionally be applied.
  • Such capsules are applied by methods known per se, for example by shaking or rolling granulation or in fluid-bed processes.
  • such granules for example by applying polymeric film-forming agent, low in dust and storage stable due to the coating.
  • a protein and / or enzyme may be particularly protected during storage against damage such as inactivation, denaturation or degradation, such as by physical influences, oxidation or proteolytic cleavage.
  • damage such as inactivation, denaturation or degradation, such as by physical influences, oxidation or proteolytic cleavage.
  • inhibition of proteolysis is particularly preferred, especially if the agents also contain proteases. Washing or treating agents may contain stabilizers for this purpose.
  • perfume oils or perfumes within the scope of the present invention, individual fragrance compounds, e.g. the synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon types are used. Preferably, however, mixtures of different fragrances are used, which together produce an attractive fragrance.
  • perfume oils may also contain natural fragrance mixtures such as are available from vegetable sources, e.g. Pine, citrus, jasmine, patchouly, rose or ylang-ylang oil.
  • a fragrance In order to be perceptible, a fragrance must be volatile, whereby besides the nature of the functional groups and the structure of the chemical compound, the molecular weight also plays an important role. For example, most odorants have molecular weights up to about 200 daltons, while molecular weights of 300 daltons and above are more of an exception. Due to the different volatility of fragrances, the smell of a perfume or fragrance composed of several fragrances changes during evaporation, whereby the odor impressions in "top note”, “middle note” or “body note” ) and “base note” (end note or dry out).
  • the top note of a perfume does not consist solely of volatile compounds, while the base note is largely made up of less volatile, i. adherent fragrances.
  • more volatile fragrances can be bound to certain fixatives, preventing them from evaporating too quickly.
  • fixatives preventing them from evaporating too quickly.
  • the fragrances can be processed directly, but it can also be advantageous to apply the fragrances on carriers that provide a slower fragrance release for long-lasting fragrance.
  • carrier materials for example cyclodextrins have been proven, wherein The cyclodextrin-perfume complexes can additionally be coated with other excipients.
  • the colorants When choosing the colorant, it must be taken into account that the colorants have a high storage stability and insensitivity to light as well as not too high an affinity for textile surfaces and, in particular, for synthetic fibers. At the same time, it should also be taken into account when choosing suitable colorants that colorants have different stabilities to the oxidation. In general, water-insoluble colorants are more stable to oxidation than water-soluble colorants. Depending on the solubility and thus also on the sensitivity to oxidation, the concentration of the colorant in the washing or treating agents varies. In the case of readily water-soluble colorants, colorant concentrations in the range of a few 10 -2 to 10 3 % by weight are typically selected. In the due to their brilliance, particularly preferred, but are less readily water-soluble pigment dyestuffs, however, the appropriate concentration of the colorant is in washing or treatment agents, typically a few 10 ⁇ 3 to 10 ⁇ 4 wt .-%.
  • Dyeing agents which can be oxidatively destroyed in the washing process and mixtures thereof with suitable blue dyes, so-called blue toners, are preferred. It has proven to be advantageous to use colorants which are soluble in water or at room temperature in liquid organic substances. Suitable examples are anionic colorants, for example anionic nitrosofarbstoffe.
  • pH adjusters In order to bring the pH of detergents or treatment agents into the desired range, the use of pH adjusters may be indicated. Can be used here are all known acids or alkalis, unless their use is not for technical application or environmental reasons or for reasons of consumer protection prohibited. Usually, the amount of these adjusting agents does not exceed 1% by weight of the total formulation.
  • Suitable foam inhibitors are, inter alia, soaps, oils, fats, paraffins or silicone oils, which may optionally be applied to support materials.
  • Suitable carrier materials are, for example, inorganic salts such as carbonates or sulfates, cellulose derivatives or silicates and mixtures of the abovementioned materials.
  • Agents preferred in the context of the present invention comprise paraffins, preferably unbranched paraffins (n-paraffins) and / or silicones, preferably linear-polymeric silicones, which are constructed according to the scheme (R 2 SiO) x and are also referred to as silicone oils.
  • silicone oils are usually clear, colorless, neutral, odorless, hydrophobic liquids having a molecular weight between 1,000 and 150,000 and viscosities between 10 and 1,000,000 mPa.s.
  • Suitable anti-redeposition agents which are also referred to as soil repellents, are, for example, nonionic cellulose ethers such as methylcellulose and methylhydroxypropylcellulose with a proportion of methoxy groups of 15 to 30% by weight and of hydroxypropyl groups of 1 to 15% by weight, based in each case on the nonionic cellulose ether and the known from the prior art polymers of phthalic acid and / or terephthalic acid or derivatives thereof, in particular polymers of ethylene terephthalates and / or polyethylene glycol terephthalates or anionic and / or nonionic modified derivatives thereof. Particularly preferred of these are the sulfonated derivatives of phthalic and terephthalic acid polymers.
  • Grayness inhibitors have the task of keeping the dirt detached from the fiber suspended in the liquor and thus preventing the dirt from being rebuilt.
  • Water-soluble colloids of mostly organic nature are suitable for this purpose, for example the water-soluble salts of polymeric carboxylic acids, glue, gelatin, salts of ether sulfonic acids or cellulose or salts of acidic sulfuric acid esters of cellulose or starch.
  • water-soluble polyamides containing acidic groups are suitable for this purpose.
  • soluble starch preparations and other than the above-mentioned starch products can be used, e.g. degraded starch, aldehyde levels, etc. Also polyvinylpyrrolidone is useful.
  • graying inhibitors are cellulose ethers such as carboxymethyl cellulose (Na salt), methyl cellulose, hydroxyalkyl cellulose and mixed ethers such as methyl hydroxyethyl cellulose, methyl hydroxypropyl cellulose, methyl carboxymethyl cellulose and mixtures thereof.
  • cellulose ethers such as carboxymethyl cellulose (Na salt), methyl cellulose, hydroxyalkyl cellulose and mixed ethers such as methyl hydroxyethyl cellulose, methyl hydroxypropyl cellulose, methyl carboxymethyl cellulose and mixtures thereof.
  • synthetic anti-crease agents can be used. These include, for example, synthetic products based on fatty acids, fatty acid esters, fatty acid amides, alkylol esters, -alkylolamides or fatty alcohols, which are usually reacted with ethylene oxide, or products based on lecithin or modified phosphoric acid ester.
  • antimicrobial agents can also be used in the portion of a washing or treatment agent portion, which is not intended to care for the automatic washing machine.
  • bacteriostatic agents and bactericides, fungicides and fungicides, etc.
  • Suitable antimicrobial agents are preferably selected from the groups of the alcohols, amines, aldehydes, antimicrobial acids or their salts, carboxylic acid esters, acid amides , Phenols, phenol derivatives, diphenyls, diphenylalkanes, urea Substance derivatives, oxygen, nitrogen acetals and formals, benzamidines, isothiazolines, phthalimide derivatives, pyridine derivatives, antimicrobial surface-active compounds, guanidines, antimicrobial amphoteric compounds, quinolines, 1, 2-dibromo-2,4-dicyanobutane, iodo-2 propynyl-butyl-carbamate, iodine, iodophores, peroxo compounds, halogen compounds and any mixtures of the above.
  • the antimicrobial active ingredient is selected from ethanol, n-propanol, isopropanol, 1,3-butanediol, phenoxyethanol, 1,2-propylene glycol, glycerol, undecylenic acid, benzoic acid, salicylic acid, dihydracetic acid, o-phenylphenol, N-methylmorpholine-acetonitrile (MMA), 2-benzyl-4-chlorophenol, 2,2'-methylenebis (6-bromo-4-chlorophenol), 4,4'-dichloro-2'-hydroxydiphenyl ether (dichlosan) , 2,4,4'-trichloro-2'-hydroxydiphenyl ether (trichloro), chlorhexidine, N- (4-chlorophenyl) -N- (3,4-dichlorophenyl) -urea, N, N '- (1, 10-decanediyldi-1-pyridinyl-4-y
  • Quaternary ammonium compounds (QAV) suitable as antimicrobial agents have the general formula (R 1 ) (R 2 ) (R 3 ) (R 4 ) N + X " , in which R 1 to R 4 are the same or different C 1 - C 22 -Alkyl radicals, C 7 -C 28 -aralkyl radicals or heterocyclic radicals, where two or, in the case of an aromatic incorporation such as in pyridine, even three radicals together with the nitrogen atom form the heterocycle, for example a pyridinium or imidazolinium compound, and X - > halide ions,
  • at least one of the radicals preferably has a chain length of 8 to 18, in particular 12 to 16, carbon atoms.
  • QACs can be prepared by reacting tertiary amines with alkylating agents, such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • alkylating agents such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • alkylating agents such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • alkylating agents such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • alkylating agents such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also
  • Suitable QAVs are, for example, benzalkonium chloride (N-alkyl-N, N-dimethylbenzylammonium chloride, CAS No. 8001-54-5), benzalkone B (m, p-dichlorobenzyl-dimethyl-C 12 -alkylammonium chloride, CAS No. 58390-78-6), benzoxonium chloride (benzyldodecylbis (2-hydroxyethyl) ammonium chloride), cetrimonium bromide (N-hexadecyl-N, N-trimethylammonium bromide, CAS No.
  • benzetonium chloride N, N-dimethyl-N- [2- [2- [p- (1,1,3,3-tetramethylbutyl) -phenoxy] ethoxy] ethyl] benzylammonium chloride, CAS no. 121-54-0
  • dialkyl dimethyl ammonium chlorides such as di-n-decyl dimethyl ammonium chloride (CAS No. 7173-51-5-5), didecyl dimethyl ammonium bromide (CAS No. 2390-68-3), dioctyl dimethyl ammonium chloride, 1-cetyl pyridinium chloride (CAS No. 123-03-5) and thiazoline iodide (CAS No.
  • QACs are the benzalkonium chlorides having C 8 -C 18 -alkyl radicals, in particular C 1 -C 4 -alkylbenzyldimethylammonium chloride.
  • bleaching compounds are bleaching compounds. These have already been described in advance.
  • the washing or treatment agent portion comprises a machine care worker.
  • the machine operator comprises care components and / or antimicrobial agents.
  • antimicrobial agents are understood here as meaning both those substances which kill microorganisms, for example bactericides and fungicides, ie also those which inhibit only the vegetation of the microorganisms, for example bacteriostats and fungistatics.
  • the machine care provider contains a combination of at least one care component and at least one antimicrobial component.
  • “Nursing component” in the sense of the present invention means that this component has water-softening and / or scale-dissolving properties and / or maintains metal, for example stainless steel, and / or rubber, for example gaskets and hoses, for example solvents such as isopropanol or ethanol for the removal of greasy soils, nonionic or anionic surfactants already mentioned, complexing agents such as thiourea and sodium thiosulfate and silicone compounds and fine polishing bodies and the components known to those skilled in the art by the term "silver corrosion inhibitors".
  • Suitable water softeners are all substances known from the prior art which are capable of complexing Ca ions.
  • Descaler are substances that are capable of dissolving limescale deposits and preferably to keep them in solution.
  • compositions may contain antioxidants.
  • This class of compounds includes, for example, substituted phenols, hydroquinones, catechols and aromatic amines, as well as organic sulfides, polysulfides, dithiocarbamates, phosphites and phosphonates.
  • UV protective substances which are applied to the treated textiles and improve the light resistance of the fibers.
  • Compounds which have these desired properties are, for example, the compounds which are active by radiationless deactivation and derivatives of benzophenone having substituents in the 2- and / or 4-position.
  • substituted benzotriazoles phenyl-substituted acrylates (cinnamic acid derivatives) in the 3-position, optionally with cyano groups in the 2-position, salicylates, organic Ni complexes and natural substances such as umbelliferone and the endogenous urocanic acid.
  • cationic active substances for example, cationic compounds of the following formulas can be used:
  • each R 1 group is independently selected from Ci -6 alkyl, alkenyl or
  • each group R is independently selected from C 8 . 28 alkyl or alkenyl groups;
  • R 3 R 1 or (CH 2 ) n -TR 2 ;
  • R 4 R 1 or R 2 or (CH 2 ) n -TR 2 ;
  • T -CH 2 -, - O-CO- or -CO-O- and n is an integer from 0 to 5.
  • Textile softening compounds can be used to care for the textiles and to improve the textile properties such as a softer feel and reduced electrostatic charge (increased wearing comfort)
  • the active ingredients of these formulations are quaternary ammonium compounds having two hydrophobic radicals, such as the disteraryldimethylammonium chloride, however because of its insufficient biodegradability, it is increasingly being replaced by quaternary ammonium compounds which contain ester groups as biodegradation breakpoints in their hydrophobic residues
  • esterquats having improved biodegradability are obtainable, for example, by mixing mixtures of methyldiethanolamine and / or triethanolamine with fatty acids esterified and the reaction products are then quaternized in a manner known per se with alkylating agents, dimethylolethyleneurea being also suitable as a finish ,
  • Phobic and impregnation processes are used to furnish textiles with substances that prevent the deposition of dirt or facilitate its leaching ability.
  • Preferred repellents and impregnating agents are perfluorinated fatty acids, also in the form of their aluminum and zirconium salts, organic silicates, silicones, polyacrylic acid esters with perfluorinated alcohol component or polymerizable compounds coupled with perfluorinated acyl or sulfonyl radical.
  • the penetration of the impregnating agent in the form of solutions or emulsions of the active substances in question can be facilitated by adding wetting agents which reduce the surface tension.
  • a further field of application of repellents and impregnating agents is the water-repellent finish of textiles, in which, in contrast to waterproofing, the fabric pores are not closed, thus the fabric remains breathable (hydrophobing).
  • the hydrophobizing agents used for hydrophobizing coat the textiles with a very thin layer of hydrophobic groups, such as longer alkyl chains or siloxane groups.
  • Suitable water repellents are, for example, paraffins, waxes, metal soaps, etc.
  • hydrophobized materials do not feel greasy; nevertheless, similar to greasy substances, water droplets emit from them without moistening.
  • silicone-impregnated textiles have a soft feel and are water and dirt repellent; Stains from ink, wine, fruit juices and the like are easier to remove.
  • Antistatic agents increase the surface conductivity and thus allow an improved drainage of formed charges.
  • External antistatic agents are generally substances with at least one hydrophilic molecule ligand and give a more or less hygroscopic film on the surfaces. These mostly surface-active antistatic agents can be subdivided into nitrogen-containing (amines, amides, quaternary ammonium compounds), phosphorus-containing (phosphoric acid esters) and sulfur-containing (alkyl sulfonates, alkyl sulfates) antistatic agents.
  • Lauryl (or stearyl) dimethylbenzylammonium chlorides are likewise suitable as antistatics for textiles or as an additive to detergents or treatment agents, wherein a softening effect is additionally achieved.
  • Silicone derivatives can be used to improve the water absorbency, rewettability of the treated fabrics, and ease of ironing the treated fabrics. These additionally improve the rinsing out of detergents or treatment agents by their foam-inhibiting properties.
  • Preferred silicone derivatives are, for example, polydialkyl or alkylaryl siloxanes in which the alkyl groups have one to five carbon atoms and are completely or partially fluorinated.
  • Preferred silicones are polydimethylsiloxanes, which may optionally be derivatized and are then amino-functional or quaternized or have Si-OH, Si-H and / or Si-Cl bonds.
  • Further preferred silicones are the polyalkylene oxide-modified polysiloxanes, ie polysiloxanes which comprise, for example, polyethylene glycols and the polyalkylene oxide-modified dimethylpolysiloxanes.
  • UV protective substances which are applied to the treated textiles and improve the light resistance of the fibers.
  • Compounds which have these desired properties are, for example, the compounds which are active by radiationless deactivation and derivatives of benzophenone having substituents in the 2- and / or 4-position.
  • substituted benzotriazoles phenyl-substituted acrylates (cinnamic acid derivatives) in the 3-position, optionally with cyano groups in the 2-position, salicylates, organic Ni complexes and natural substances such as umbelliferone and the endogenous urocanic acid.
  • Optical brighteners may be added to the washing or treating agents to eliminate graying and yellowing of the treated fabrics. These fabrics impinge on the fiber and cause whitening and bleaching by transforming invisible ultraviolet radiation into visible longer wavelength light, emitting the ultraviolet light absorbed from the sunlight as faint bluish fluorescence, and pure with the yellowness of the grayed or yellowed wash White results.
  • Suitable compounds originate from the substance classes of the 4,4 'diamino-2,2-stilbenedisulfonic acids (flavonic), 4,4'-biphenylene -Distyryl, liferone Methylumbel-, coumarins, dihydroquinolinones, 1, 3-diaryl pyrazolines, naphthalimides, Benzoxazole, Benzisoxazol- and benzimidazole systems and substituted by heterocycles pyrene derivatives.
  • flavonic 4,4'diamino-2,2-stilbenedisulfonic acids
  • 4,4'-biphenylene -Distyryl liferone Methylumbel-
  • coumarins dihydroquinolinones
  • 1, 3-diaryl pyrazolines 1, 3-diaryl pyrazolines
  • naphthalimides Benzoxazole
  • Benzisoxazol- and benzimidazole systems substituted by
  • washing or treatment agent portions according to the invention show a higher performance .
  • a washing or treating agent portion according to the invention preferably contains pressed material, which preferably has substantially the same washing or treating agent composition as the other layers.
  • the detergent or treatment agent portion comprises a core which differs in composition from the composition of the remaining detergent or treatment agent portion.
  • the core preferably comprises a machine care worker, which preferably comprises a combination of at least one care component and at least one antimicrobial component.
  • sterilization of the automatic washing machine can be counteracted and / or the interior of the automatic washing machine can be maintained by releasing a disinfecting / nourishing substance after a number (n) of washing or treatment cycles in a further (n + 1st) washing or treatment cycle ,
  • the washing or treatment agent portion contains a active substance-containing core comprising a machine guard, which only comes into contact after dissolving the active substance-containing coating layer with the environment.
  • the core contains other washing or treatment-active substances in addition to the machine care worker, so that even in the last washing or treatment cycle with the washing or treatment agent portion according to the invention, in which the machine guard is released, textiles can be washed and / or treated.
  • the machine care agent may also be contained in a washing or treating agent phase outside the invention and thus released before dissolving / dispersing the washing or treating agent.
  • the automatic washing machine is maintained / disinfected in the first washing or treatment cycle, which is carried out with the washing or treatment agent portion according to the invention.
  • the washing or treating agent for the textiles is preferably released only in the washing or treatment courses following this first washing or treatment course.
  • the active-material-containing coating layer contains a washing or treating agent and additionally a machine guard so that even in the first washing or treatment cycle in which the washing or treating agent portion according to the invention is used, textiles are washed and / or or can be treated.
  • the active substance-containing core of the washing or departmentsmittelportion comprises a machine care worker who comes into contact after dissolving the active substance-containing shell layer with the environment and which preferably water-softening substances and / or E-delstahlskyr and / or care agents for elastic parts and / or agents from the Group of substances that kill microorganisms or inhibit their vegetation. Suitable nourishing and antimicrobial components have already been mentioned.
  • the separation of different fragrance compositions and the controlled resolution maximum one, preferably exactly one active substance-containing layer and thus the targeted release of a defined amount of active material can be achieved, for example, that exist between the individual active substance-containing layers barrier layers, preferably a deviating from the active substance-containing layers solubility - or have dispersing behavior.
  • Suitable materials for these barrier layers have already been listed under the terms “solubility control system” and "(physicochemical) chemical switch”. To avoid repetition, please refer to the corresponding text passages.
  • barrier layers which dissolve / disperse predominantly in heated water and thus in the actual washing or treatment cycle are preferred, as well as those which are predominantly in the rinsing cycle, owing to the lower ionic strength and / or the lower pH Value can be dissolved / dispersed.
  • Barrier layers containing a (physico-) chemical switch are preferably used in washing or treating agent portions according to the invention which have a plurality of active substance-containing layers whose active substances are to be released in a washing or treatment cycle carried out with heated water and which has a system for controlling the Contain solubility as defined above.
  • suitable active substances are the substances mentioned in advance under the term "basic detergents" or also bleaching or enzyme components.
  • Barrier layers having a (physico-) chemical switch allow an active-material-containing layer applied outside the barrier layer to be dissolved / dispersed and thus consumed in a washing cycle treated with heated water, due to the barrier layer during the washing or treatment cycle However, the increased ionic strength and / or the increased pH remains intact. In this case, the barrier layer dissolves / disperses in the subsequent rinsing cycle, in which the ionic strength and / or the pH drops, or disperses, thus allowing contact of the active substance-containing layer below the barrier layer with the water. If this layer in turn has a higher solubility / dispersibility in a washing or treatment cycle than in a rinsing cycle, the active substance contained in this layer will not be released until the next washing or treatment cycle.
  • Barrier layers which have a temperature-dependent solubility / dispersibility are preferably used in washing or treating agent portions according to the invention which have a plurality of active substance-containing layers but whose active substances are to be released in the rinse and which preferably contain a (physico-) chemical switch.
  • suitable active substances are the substances mentioned in advance under the term "equipment components".
  • Crevices having a solubility control system which provides a significantly higher temperature solubility / dispersibility enable an active-substance containing layer applied outside the barrier layer to be in a rinse cycle, that of cold water preferably at low ionic strength and / or low pH is carried out, dissolved / dispersed and thus consumed, the barrier layer remains intact during the Spülzyklus- ses due to the low temperature.
  • the barrier layer dissolves / disperses in the subsequent washing or treatment cycle, which is carried out with heated water, and thus enables the contact of the active substance-containing layer located below the barrier layer with the water.
  • the active substance contained in this layer will not be released until the next rinsing cycle.
  • the barrier layer only performs insulating tasks, then the washing or treating agent portion according to the invention releases active substance only in the rinsing cycles.
  • the barrier layer contains a base detergent which is dissolved / dispersed together with the insulating barrier material.
  • this washing or treating agent portion according to the invention releases base detergent (or also an additional component for a base detergent) and, in the rinsing cycles, an equipment component for textiles.
  • the barrier layers preferably contain polymeric compounds, preferably polycarbonates and in particular (modified) polyacrylates.
  • the barrier layers preferably have a thickness of at most 1, 0 mm, more preferably of at most 0.7 mm and in particular of not more than 0.4 mm.
  • barrier layer between the active substance-containing core and the adjacent layer which has a lower water solubility / water dispersibility than further barrier layers which are located in the washing or treatment agent portion.
  • the water solubility / water dispersibility of the barrier layers can be controlled, for example, by the degree of crosslinking of the polymers used as the barrier layer component, the choice of substituents of the polymer backbone, and the molecular weight of the polymers.
  • the barrier layer located between the active substance-containing core and the adjacent coating layer preferably dissolves / disperses only in an aqueous medium, if this has a temperature of at least 30 ° C., preferably at least 40 ° C., more preferably at least 50 ° C., more preferably at least 60 ° C and in particular of at least 90 0 C.
  • the barrier layer located between the active substance-containing core and the adjacent enveloping layer can / must be removed manually.
  • the barrier layer between the active substance-containing core and the adjacent active substance-containing layer is colored and thus has an indicator effect. In this way, the consumer can recognize when the active substance-containing layers of the washing or treatment agent portion according to the invention are consumed and thus the active substance-containing core - preferably for the care of the automatic washing machine - used and a corresponding washing or treatment program of the automatic washing machine can be selected.
  • At least one strip, wedge and / or other volume is in at least one component or the concentration of at least one component of the composition (s) of the active agent containing core and / or the remaining washing or treatment agent portion, ie the active substance-containing layer.
  • the washing or treatment agent according to the invention substantially in the form of a prism, preferably a cuboid or ellipsoid, preferably a spheroid, in particular a flattened or prolapsed spheroid or a sphere and the further (n) phase ( n), preferably in the form of a cylinder, cuboid, cone, pyramid, ellipsoid or irregular volume in the washing or treating agent portion, the further phase (s) preferably extending radially in the washing or treating agent portion / extend.
  • the further phase (s) extends / extend essentially from the center of the washing or treatment agent portion to the surface of the washing or treatment agent portion, wherein the tip of the respective spatial form (cone, pyramid) is preferably substantially in the center of the washing or treatment agent portion is located.
  • the further phase (s) are preferably solid or highly viscous and thus dimensionally stable.
  • the further phase (s) and the remaining washing or treating agent portion have comparable dissolving / dispersing properties.
  • the active ingredients of the cladding layer (s) and the other (s) phases in the same cycle so preferably released either in the washing or treatment cycle or in the rinse cycle.
  • An example of a corresponding washing or treating agent portion according to the invention is a portion which comprises in one or more active substance-containing coating layer (s) a base detergent for white and / or colored textiles, sensitive textiles and / or wool and which additionally has at least one volume, which is preferably in the form of a cone extending from the center of the detergent or treating agent portion to the surface thereof and comprising an additive component for a washing or treating agent, preferably a bleach, enzyme or softening composition for textiles.
  • a detergent or treating agent portion which comprises an enzyme-containing, but substantially bleach-free, composition in the active substance-containing coating layer (s) and which additionally contains at least one volume in which a substantially enzyme-free bleaching composition is contained vice versa.
  • a washing or treating agent portion which, within the coating layer (s), contains a base detergent, in a volume which preferably extends in the form of a cone from the middle of the washing or treating agent portion to the surface thereof, a bleaching composition. and another volume, which also preferably extends radially in the portion, containing an enzyme composition.
  • An advantage of these embodiments is the ability to separate incompatible ingredients that are to be released at the same time, for example, the separation of bleach and enzyme or bleach and dyes and / or fragrances and other sensitive components.
  • the further phase (s) and the active ingredient-containing shell layer (s) have opposite dissolving / dispersing properties, so that the active substance-containing shell layer (s) is dissolved / dispersed in the washing or treatment cycle while the other phase (s) release active in the rinse cycle or vice versa.
  • An example of a corresponding washing or treating agent portion according to the invention is a portion which comprises in one or more active substance-containing coating layer (s) a base detergent for white and / or colored textiles, sensitive textiles and / or wool and which additionally has at least one volume, which is preferably in the form of a cone extending from the center of the detergent or treating agent portion to the surface thereof and an equipment component, preferably a plasticizer compound, soil repellent polymers, repellents or impregnating agents, antistatic agents, optical brighteners, compounds which improve the water absorbency, the Renewability of the treated textiles and the ease of Bügeins serve the treated textiles and / or fragrances.
  • a washing or treating agent portion which comprises an enzyme-containing, but substantially bleach-free composition in the active substance-containing coating layer (s) and which additionally contains at least one volume in which an equipment component is contained or vice versa.
  • An example of a detergent or treating agent portion of the present invention is a portion comprising a active agent-containing core containing a machine care agent and comprising 4 further coating layers arranged to decrease the solubility / dispersibility of the coating layers towards the surface of the portion ,
  • the cladding layers in this embodiment each comprise 65% by weight of a washing or treatment active composition
  • This composition is present in homogeneous blend with 35% by weight of different solubility control systems.
  • the first, ie innermost shell layer comprises 35% by weight PEG 4000
  • the second layer following the first shell layer comprises 35% by weight PEG 12000
  • the third layer following the second shell layer comprises 35% by weight of one 1: 2.5 mixture of paraffin (melting range 42-44 ° C) and PEG 12000
  • the outer shell layer comprises 35 wt .-% paraffin (melting range 42-44 ° C).
  • a further subject of the present invention is a process for producing a washing or treating agent portion according to the invention, comprising the following steps: a) providing a core, preferably by means of melt casting, tableting or extrusion; b) wrapping the core with 1 to 59, preferably 3 to 49 and in particular 5 to 39 layers, the layers preferably by hardening of flowable masses due to temperature reduction, incorporation of water of hydration or other solvent components, reaction of components contained in the flowable materials, modification conversions , Evaporation of water or other solvent components, condensation, irradiation or by compression in such an order that the detergent or treating agent portion has a solubility and / or dispersibility gradient, preferably the solubility and / or dispersibility of the individual layers and the core decreases radially towards the surface of the washing or treatment agent portion.
  • a step c) is carried out between step a) and step b) and / or between several steps b) in which a barrier layer is obtained by melt solidification, incorporation of water of hydration or other solvent components, reaction of components contained in the barrier material, modification conversions, Evaporation of water or other solvent components, condensation, irradiation or by pressing on the respective outer layer of the agent is applied.
  • the structure of the layers of a washing or treating agent portion can be carried out, for example, by immersing the core in a melt, solution or dispersion comprising the constituents of the washing or treating agent composition or its precursor constituents. Furthermore, it is possible to fix the core in a mold, preferably in the middle of the mold, and to pour the flowable components or precursor constituents of the laundry or treating agent composition into the mold, so that the core is completely enclosed by the cast-in material. Curing of the cast-in material preferably takes place for the portion according to the invention Drying, ie evaporation of water or other solvents, incorporation of water of hydration or melt solidification due to temperature reduction instead. Another possibility for enveloping the active substance-containing core is spraying the core with a sprayable preparation comprising the constituents or precursor constituents of the washing or treating agent composition.
  • the present invention also relates to a kit comprising a washing or treating agent portion according to the invention and a bag of water-permeable material or a rigid at least in areas container with one or more opening (s), through which liquids, but not the washing or treatment agent portion in undissolved , non-dispersed and non-pulverized form, can enter and exit.
  • a kit comprising a washing or treating agent portion according to the invention and a bag of water-permeable material or a rigid at least in areas container with one or more opening (s), through which liquids, but not the washing or treatment agent portion in undissolved , non-dispersed and non-pulverized form, can enter and exit.
  • the bag or the container is at least partially permeable to water, so that when the kit is used in an automatic washing machine, water, aqueous solutions and dispersions of the washing or treatment agent active substances can enter and leave through these openings.
  • the diameter of the openings for water / wash liquor is between 0.1 and 1 cm, in particular 0.2 and 0.5 cm, so that the exchange of dissolved and / or dispersed components of the washing or treatment agent portion done, but not the Treatment agent portion in undissolved, non-dispersed, not pulverized form from the envelope or the bag can escape.
  • the material of the bag is elastic and adapts to the decreasing size of the washing or treating agent portion with the number of washing or treatment courses.
  • the bag or container prevents direct contact of the washing or treating agent portion with the textile during the washing or treatment process as well as in the period between completion of the washing or treatment process and removal of the washed or treated textiles from the automatic washing machine by the consumer. Further, the bag or container controls the dissolution / dispersion of the detergent or treating agent portion because the surface of the detergent or treating agent portion contacts less water / wash liquor due to limited fluid passage through the bag / container material than does the direct use of the wash - or treatment agent portion in the washing drum of an automatic washing machine would be the case.
  • An additional protection of the washing or treatment agent portion from the mechanical influences A washing or treatment cycle is achieved by the introduction of cushioning material, preferably of water-permeable foam or fleece.
  • the kit comprises a bag which contains an inner and an outer layer of a net-like material and an intermediate layer of a cushioning material, preferably foam, and is preferably elastic.
  • the bag or container preferably has a device that allows the closure of the enclosure. Preference is given to devices in which a tape or a cord is passed through a channel along the upper edge of the bag, which can be pulled together and Corpnürrt or clamped together.
  • a method for washing and / or treating textiles in an automatic washing machine in which a washing or treating agent portion according to the invention or a kit according to the invention is introduced into the drum of the washing machine and a washing or treatment program of the washing machine is started is a further subject matter of the present invention Invention.
  • the washing or treating agent portion according to the invention or the kit according to the invention in the washing machine drum exposes the water to from 2 to 60, preferably from 4 to 50 and in particular from 6 to 40 washing or treatment cycles, the active substance-containing phases of the washing agent dissolving and / or disperse and the active substance contained is released.
  • the washing or treating agent portion comprises a base detergent for white and / or colored textiles, delicate textiles and / or wool
  • the portion preferably in the form of the described kit, preferably the water is from 2 to 40, preferably 4 to 30 and in particular 6 to 20 washing or treatment courses suspended and / or is used in addition to an additive component for a base detergent, such as an enzyme, bleach or equipment component as defined above in an automatic washing machine for textiles.
  • the washing or treating agent portion contains an additional component for a basic detergent
  • the portion preferably in the form of the described kit, is preferably exposed to the water from 5 to 60, preferably from 10 to 50, and in particular from 15 to 40, washing or treatment courses and / or additionally to a basic detergent for white and / or colored textiles, delicate textiles and / or wool used in an automatic washing machine for textiles.
  • the optionally contained ak- tivstoffumble core dissolved and / or dispersed and preferably disinfected and / or maintained the automatic washing machine with the liberated active ingredients.
  • Particularly good cleaning and / or care results are obtained when the core in a washing or treatment cycle without textiles at least 18 ° C, preferably at least 30 0 C, more preferably at least 40 0 C, preferably at least 50 0 C, very particularly preferably at least 60 0 C and in particular at 90 0 C is dissolved or dispersed.
  • the active agent-containing core preferentially dissolves / disperses only after a barrier layer has been dissolved and / or dispersed or removed manually between the active-containing core and the adjacent coating layer.
  • Another object of the present invention is the use of a washing or treating agent portion according to the invention or a kit according to the invention for automatic dosing in the drum of an automatic washing machine for textiles.
  • a washing agent or treating agent portion according to the invention or the kit according to the invention is used in 2 to 60, preferably 4 to 50 and in particular more than 6 to 40 washing or treatment courses.
  • a dimensionally stable one-piece washing or treating agent portion having a mass of at least 50 g, comprising a base detergent for white and / or colored textiles, delicate textiles and / or wool, as well as a fully enclosed active substance-containing core, at least in one component or the concentration of at least one constituent of the composition of the active substance-containing cladding layer, wherein the washing or treating agent portion has a radially extending solubility or dispersibility gradients, used alone or together with an additional component for a base detergent in an automatic washing machine and there for washing and / or treating textiles.
  • the active substance-containing core contained in the washing or treating agent portion according to the invention is used for caring and / or disinfecting the automatic washing machine following the washing or treatment cycles in which the active substance-containing coating layer dissolves or disperses.
  • the washing or treating agent portion of the invention is - preferably enclosed by a bag - metered directly into the drum of the washing machine and left there for 2 to 40 washing or treatment courses.
  • the additional component for the basic detergent can be dosed via the dispenser or also directly into the drum of the automatic washing machine.
  • the additional component for the base detergent is also in the form of a dimensionally stable, one-piece treatment agent portion having a mass of at least 50 g, which provides active ingredient for 5 to 60 washing or treatment courses and which preferably also has a radially extending solubility or dispersibility gradients.
  • a dimensionally stable one-piece washing or treating agent portion having a mass of at least 50 g, comprising an additional component for a washing or treating agent, preferably an enzyme, bleaching or finishing component, and a fully enclosed active substance-containing core, which differs at least in one constituent or in the concentration of at least one constituent from the composition of the active substance-containing enveloping layer, wherein the washing or treating agent portion has a radially extending solubility or dispersibility gradient, alone or together with a base detergent for white and / or colored textiles , delicate textiles and / or wool used in an automatic washing machine and used there for washing and / or treating textiles.
  • the active substance-containing core contained in the washing or treating agent portion according to the invention is used for caring and / or disinfecting the automatic washing machine following the washing or treatment cycles in which the active substance-containing coating layer dissolves or disperses.
  • the washing or treating agent portion according to the invention is - preferably enclosed by a bag - dosed directly into the drum of the washing machine and left there for 5 to 60 washing or treatment courses.
  • the basic detergent can be dosed via the dispenser or also directly into the drum of the automatic washing machine.
  • the base detergent is also in the form of a dimensionally stable, one-part treatment agent portion having a mass of at least 50 g, which provides active ingredient for 2 to 40 washing or treatment courses and which preferably also has a radially extending solubility or dispersibility gradients.
  • washing or treating agent portion comprising a base detergent in an automatic washing machine for washing and / or treating textiles.
  • washing or treating agent portions according to the invention comprising bleach, enzyme and / or equipment components are metered into the washing or treating agent portion comprising the base washing agent, so that these portions are used together for washing and / or treating textiles in an automatic washing machine.
  • the detergent or treating agent portions individually in a bag or container in the drum of an automatic washing machine.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

L'invention concerne une portion monobloc de forme stable de détergent ou de produit traitant, dont la masse est d'au moins 50 g, qui présente un gradient de solubilité et/ou de dispersibilité. Cette portion permet la libération d'une quantité stable de substance active, même lorsque sa surface diminue.
PCT/EP2007/054977 2006-06-27 2007-05-23 Portion de détergent ou de produit traitant à gradient de solubilité et/ou de dispersibilité WO2008000562A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006029838A DE102006029838A1 (de) 2006-06-27 2006-06-27 Wasch- oder Behandlungsmittelportion mit Löslichkeits- und/oder Dispergierfähigkeitsgradient
DE102006029838.1 2006-06-27

Publications (1)

Publication Number Publication Date
WO2008000562A1 true WO2008000562A1 (fr) 2008-01-03

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PCT/EP2007/054977 WO2008000562A1 (fr) 2006-06-27 2007-05-23 Portion de détergent ou de produit traitant à gradient de solubilité et/ou de dispersibilité

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DE (1) DE102006029838A1 (fr)
WO (1) WO2008000562A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190066067A (ko) 2016-10-21 2019-06-12 바이오콘 리미티드 루푸스 치료를 위한 단일클론항체 및 이의 치료방법

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3407144A (en) * 1963-12-11 1968-10-22 Procter & Gamble Detergent composition
US5759988A (en) * 1993-12-30 1998-06-02 Ecolab Inc. Stable hygroscopic detergent article
WO2001042416A1 (fr) * 1999-12-10 2001-06-14 Henkel Kommanditgesellschaft Auf Aktien Procede de pressage pour corps moules multiphases
US6462007B1 (en) * 1998-01-26 2002-10-08 The Procter & Gamble Company Multi-layer detergent tablet
DE10134309A1 (de) * 2001-07-14 2003-02-06 Henkel Kgaa Coextrusion von Wasch- und Reinigungsmitteln
WO2005077064A2 (fr) * 2004-02-10 2005-08-25 Eco-Safe Technologies, L.L.C. Composition et dispositif de nettoyage solide, polyvalents

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3407144A (en) * 1963-12-11 1968-10-22 Procter & Gamble Detergent composition
US5759988A (en) * 1993-12-30 1998-06-02 Ecolab Inc. Stable hygroscopic detergent article
US6462007B1 (en) * 1998-01-26 2002-10-08 The Procter & Gamble Company Multi-layer detergent tablet
WO2001042416A1 (fr) * 1999-12-10 2001-06-14 Henkel Kommanditgesellschaft Auf Aktien Procede de pressage pour corps moules multiphases
DE10134309A1 (de) * 2001-07-14 2003-02-06 Henkel Kgaa Coextrusion von Wasch- und Reinigungsmitteln
WO2005077064A2 (fr) * 2004-02-10 2005-08-25 Eco-Safe Technologies, L.L.C. Composition et dispositif de nettoyage solide, polyvalents

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190066067A (ko) 2016-10-21 2019-06-12 바이오콘 리미티드 루푸스 치료를 위한 단일클론항체 및 이의 치료방법

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