EP3325597B1 - Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes - Google Patents

Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes Download PDF

Info

Publication number
EP3325597B1
EP3325597B1 EP16741307.9A EP16741307A EP3325597B1 EP 3325597 B1 EP3325597 B1 EP 3325597B1 EP 16741307 A EP16741307 A EP 16741307A EP 3325597 B1 EP3325597 B1 EP 3325597B1
Authority
EP
European Patent Office
Prior art keywords
acid
dishwasher detergent
automatic dishwasher
weight
enzyme
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP16741307.9A
Other languages
German (de)
English (en)
Other versions
EP3325597A1 (fr
Inventor
Inga Kerstin Vockenroth
Johannes Zipfel
Silke Menke
Thomas Weber
Noelle Wrubbel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56497769&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3325597(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to PL16741307T priority Critical patent/PL3325597T3/pl
Publication of EP3325597A1 publication Critical patent/EP3325597A1/fr
Application granted granted Critical
Publication of EP3325597B1 publication Critical patent/EP3325597B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3907Organic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0073Tablets
    • C11D17/0078Multilayered tablets
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/042Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • C11D17/045Multi-compartment
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase

Definitions

  • the present invention relates to a machine dishwashing detergent which exhibits improved cleaning performance, in particular on enzyme-sensitive soiling, the use of this dishwashing agent and a method for machine dishwashing using this dishwashing agent.
  • EP 2 217 690 A1 describes a composition comprising an enzyme and a bleaching compound, the enzyme and the bleaching compound being formulated in separate areas, ie spatially separated from one another, since this separation has a positive effect on the stability of the enzyme.
  • a builder is also contained in the enzyme area, the builder comprising methylglycinediacetic acid (MGDA).
  • MGDA methylglycinediacetic acid
  • Other multi-phase dishwashing detergents containing MGDA are from US 2014/0018278 A1 , DE 102013225485 A1 and US 2013/0199569 A1 known.
  • the object of the present invention was to provide a, preferably phosphate-free, machine dishwashing detergent which has a further increased cleaning performance.
  • a first object of the present invention is therefore a machine dishwashing detergent, comprising (A) an enzyme phase, the enzyme phase containing at least one enzyme and being essentially free of bleaching agents and organic builders from the class of the aminocarboxylic acids and their salts; and (B) a bleaching phase, the bleaching phase containing at least one bleaching agent, at least one bleaching catalyst and at least one organic builder from the class of aminocarboxylic acids and their salts, in particular methylglycinediacetic acid (MGDA) or its salts.
  • MGDA methylglycinediacetic acid
  • the present invention also relates to the use of an automatic dishwashing agent according to the invention in an automatic dishwashing process, in particular the use to improve the cleaning performance of enzyme-sensitive soiling on dishes when cleaning them in an automatic dishwasher.
  • the present invention also relates to a machine dishwashing method in which an automatic dishwashing agent according to the invention is used in particular for the purpose of improving the cleaning performance of enzyme-sensitive soiling.
  • At least one as used herein means 1 or more, ie 1, 2, 3, 4, 5, 6, 7, 8, 9 or more.
  • the information refers to the type of ingredient and not to the absolute number of molecules.
  • At least one bleaching catalyst thus means, for example, at least one type of bleaching catalyst, ie that one type of bleaching catalyst or a mixture of several different bleaching catalysts can be meant.
  • the information relates to all compounds of the specified type which are contained in the composition / mixture, ie that the composition contains no further compounds of this type beyond the specified amount of the corresponding compounds.
  • the number average molecular weight can be determined, for example, by means of gel permeation chromatography (GPC) in accordance with DIN 55672-1: 2007-08 with THF as the eluent.
  • GPC gel permeation chromatography
  • the mass average molecular weight M w can also be determined by means of GPC, as described for M n .
  • Substantially free of or “Free of” as used herein means that the ingredient in question is present in the appropriate phase or agent in a negligible amount, especially in an amount that is insufficient for the typical functionality of the ingredient is.
  • the enzyme phase is preferably "essentially free of MGDA or its salts".
  • this information relates to amounts of 1% by weight or less, preferably 0.5% by weight or less, more preferably 0.1% by weight or less, more preferably 0.01% by weight or less , most preferably 0.001 wt% or less or 0.0001 wt% or less, each based on the weight of the enzyme phase.
  • Corresponding amounts also apply to the expression "phosphate-free", the abovementioned proportions by weight in each case based on the total cleaning agent.
  • the bleaching phase is preferably “essentially free of enzymes”.
  • this information relates to amounts of enzyme protein of 0.1% by weight or less, preferably 0.05% by weight or less, more preferably 0.01% by weight or less, more preferably 0.001% by weight or less, most preferably 0.0005% or less or 0.0001% or less, each based on the weight of the bleach phase.
  • fatty acids or fatty alcohols or their derivatives are representative of branched or unbranched carboxylic acids or alcohols or their derivatives with preferably 6 to 22 carbon atoms.
  • the oxo alcohols or their derivatives obtainable, for example, according to RoELEN's oxo synthesis can also be used accordingly.
  • alkaline earth metals are mentioned in the following as counterions for monovalent anions, this means that the alkaline earth metal is naturally only present in half the amount of the substance - sufficient to balance the charge - like the anion.
  • the agents of the present invention contain at least one enzyme, preferably in the form of an enzyme preparation or enzyme composition, which can contain one or more enzymes.
  • Suitable enzymes include, but are not limited to, proteases, amylases, lipases, hemicellulases, cellulases, perhydrolases or oxidoreductases, and preferably mixtures thereof.
  • these enzymes are of natural origin; Based on the natural molecules, improved variants are available for use in cleaning agents, which are accordingly preferred.
  • Cleaning agents according to the invention preferably contain enzymes in total amounts of 1 ⁇ 10 -6 to 5% by weight, based on active protein.
  • the protein concentration can be determined using known methods, for example the BCA method or the biuret method.
  • proteases are among the most technically significant enzymes. They are the longest established enzymes for detergents and cleaning agents and are found in practically all modern, powerful detergents and cleaning agents. They break down protein-based soiling on the items to be cleaned. Of these, proteases of the subtilisin type (subtilases, subtilopeptidases, EC 3.4.21.62) are particularly important, which are serine proteases due to the catalytically active amino acids. They act as non-specific endopeptidases and hydrolyze any acid amide bonds that are inside peptides or proteins. Their pH optimum is usually in the clearly alkaline range. An overview of this family can be found in the article " Subtilases: Subtilisin-like Proteases "by R.
  • subtilisin enzymes edited by R. Bott and C. Betzel, New York, 1996 .
  • Subtilases are naturally formed by microorganisms. Among these, the subtilisins formed and secreted by Bacillus species are to be mentioned as the most important group within the subtilases.
  • proteases of the subtilisin type which are preferably used in washing and cleaning agents are the subtilisins BPN 'and Carlsberg, the protease PB92, the subtilisins 147 and 309, the protease from Bacillus lentus, in particular from Bacillus lentus DSM 5483, Subtilisin DY and the subtilases, but no longer the subtilisins in the narrower sense enzymes Thermitase, Proteinase K and the proteases TW3 and TW7, and variants of the proteases mentioned which have an amino acid sequence which is different from that of the starting protease.
  • Proteases are changed in a targeted or random manner by methods known from the prior art and are thus optimized, for example, for use in detergents and cleaning agents. This includes point mutagenesis, deletion or insertion mutagenesis or fusion with other proteins or protein parts. Correspondingly optimized variants are known for most proteases known from the prior art.
  • amylases which can be used according to the invention are the ⁇ -amylases from Bacillus licheniformis, from B. amyloliquefaciens, from B. stearothermophilus, from Aspergillus niger and A. oryzae, and the further developments of the aforementioned amylases which are improved for use in cleaning agents. Furthermore, the ⁇ -amylase from Bacillus sp. A 7-7 (DSM 12368) and the cyclodextrin glucanotransferase (CGTase) from B. agaradherens (DSM 9948).
  • Lipases or cutinases can also be used according to the invention, in particular because of their triglyceride-cleaving activities, but also to generate peracids in situ from suitable precursors.
  • suitable precursors include, for example, the lipases originally obtainable from Humicola lanuginosa (Thermomyces lanuginosus) or further developed, in particular those with the amino acid exchange D96L, T213R and / or N233R, particularly preferably all of the exchanges D96L, T213R and N233R.
  • oxidoreductases for example oxidases, oxygenases, catalases, peroxidases, such as halo-, chloro-, bromo-, lignin, glucose or manganese peroxidases, dioxygenases or laccases (phenoloxidases, polyphenol oxidases) can be used according to the invention.
  • organic, particularly preferably aromatic, compounds interacting with the enzymes are additionally added in order to increase the activity of the oxidoreductases in question (enhancers) or to ensure the flow of electrons (mediators) in the case of very different redox potentials between the oxidizing enzymes and the soiling.
  • the agent contains at least one protease and, preferably, also at least one amylase.
  • a protein and / or enzyme can be protected against damage, such as inactivation, denaturation or decay, for example by physical influences, oxidation or proteolytic cleavage, especially during storage.
  • damage such as inactivation, denaturation or decay, for example by physical influences, oxidation or proteolytic cleavage, especially during storage.
  • the proteins and / or enzymes are obtained microbially, inhibition of proteolysis is particularly preferred, in particular if the agents also contain proteases.
  • Detergents can contain stabilizers for this purpose; the provision of such agents is a preferred embodiment of the present invention.
  • Proteases and amylases that are active in cleaning are generally not provided in the form of the pure protein but rather in the form of stabilized, storable and transportable preparations.
  • These prefabricated preparations include, for example, the solid preparations obtained by granulation, extrusion or lyophilization or, particularly in the case of liquid or gel form agents, solutions of the enzymes, advantageously as concentrated as possible, low in water and / or mixed with stabilizers or other auxiliaries.
  • the enzymes can be encapsulated both for the solid and for the liquid dosage form, for example by spray drying or extrusion of the enzyme solution together with a preferably natural polymer or in the form of capsules, for example those in which the enzymes are enclosed as in a solidified gel or in those of the core-shell type in which an enzyme-containing core is coated with a protective layer impermeable to water, air and / or chemicals.
  • Additional active ingredients for example stabilizers, emulsifiers, pigments, bleaching agents or dyes, can additionally be applied in superimposed layers.
  • Capsules of this type are applied by methods known per se, for example by shaking or roll granulation or in fluid-bed processes. Such granules are advantageously low in dust, for example by applying polymeric film formers, and are stable on storage due to the coating.
  • the enzyme protein forms only a fraction of the total weight of conventional enzyme preparations.
  • Protease and amylase preparations preferably used according to the invention contain between 0.1 and 40% by weight, preferably between 0.2 and 30% by weight, particularly preferably between 0.4 and 20% by weight and in particular between 0, 8 and 10% by weight of the enzyme protein.
  • compositions which, based on their total weight, contain 0.1 to 12% by weight, preferably 0.2 to 10% by weight and in particular 0.5 to 8% by weight of enzyme preparations.
  • the weight information on enzymes means the amount of active enzyme protein based on the total mass of the entire composition.
  • the enzyme phase contains at least 0.0001% by weight, preferably at least 0.001% by weight, in particular at least 0.01% by weight, particularly preferably at least 0.05% by weight, very particularly preferably at least 0 , 1 wt% protease per gram of total composition.
  • the enzyme phase contains at least 0.0001% by weight, preferably at least 0.0005% by weight, in particular at least 0.001% by weight, particularly preferably at least 0.005% by weight, very particularly preferably at least 0.01 % By weight of amylase per gram of the total composition.
  • the enzyme phase contains at least 0.0005% by weight, in particular at least 0.001% by weight, particularly preferably at least 0.005% by weight, very particularly preferably at least 0.01% by weight of amylase per gram of the total composition and at least 0.001% by weight, in particular at least 0.01% by weight, particularly preferably at least 0.05% by weight, very particularly preferably at least 0.1% by weight of protease per gram of the total composition.
  • compositions described herein can also include enzyme stabilizers.
  • a group of stabilizers are reversible protease inhibitors. Benzamidine hydrochloride, borax, boric acids, boronic acids or their salts or esters are frequently used for this, including above all derivatives with aromatic groups, for example ortho-, meta- or para-substituted phenylboronic acids, in particular 4-formylphenyl-boronic acid, or the salts or Esters of the compounds mentioned.
  • Peptide aldehydes, ie oligopeptides with a reduced C-terminus, in particular those of 2 to 50 monomers, or their hydrogen sulfite adducts are also used for this purpose.
  • the peptide reversible protease inhibitors include, among others, ovomucoid and leupeptin. Specific, reversible peptide inhibitors for the protease subtilisin as well as fusion proteins from proteases and specific peptide inhibitors are also suitable for this.
  • Further enzyme stabilizers are amino alcohols such as mono-, di-, triethanol- and -propanolamine and their mixtures, aliphatic carboxylic acids up to C 12 , such as succinic acid, other dicarboxylic acids or salts of the acids mentioned. End-capped fatty acid amide alkoxylates are also suitable for this purpose. Further enzyme stabilizers are known to the person skilled in the art from the prior art.
  • the bleaching catalysts which can be used according to the invention include, but are not limited to, the group of bleach-enhancing transition metal salts and transition metal complexes, preferably Mn, Fe, Co, Ru or Mo salt complexes or carbonyl complexes. Mn, Fe, Co, Ru, Mo, Ti, V and Cu complexes with N-containing tripod ligands as well as Co, Fe, Cu and Ru amine complexes can also be used as bleaching catalysts.
  • Complexes of manganese in oxidation state II, III, IV or IV are particularly preferably used, which preferably contain one or more macrocyclic ligand (s) with the donor functions N, NR, PR, O and / or S.
  • Ligands which have nitrogen donor functions are preferably used.
  • bleaching catalyst (s) in the agents according to the invention which contain 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN), 1,4,7-triazacyclononane (TACN) as macromolecular ligands ), 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 contain 2-methyl-1,4,7-triazacyclononane (Me / TACN).
  • Me-TACN 1,4,7-trimethyl-1,4,7-triazacyclononane
  • TACN 1,4,7-triazacyclononane
  • Suitable manganese complexes are, for example, [Mn III 2 ( ⁇ -O) 1 ( ⁇ -OAc) 2 (TACN) 2 ] (ClO 4 ) 2 , [Mn III Mn IV ( ⁇ -O) 2 ( ⁇ -OAc) 1 (TACN ) 2 ] (BPh 4 ) 2 , [Mn IV 4 ( ⁇ -O) 6 (TACN) 4 ] (ClO 4 ) 4 , [Mn III 2 ( ⁇ -O) 1 ( ⁇ -OAc) 2 (Me-TACN ) 2 ] (ClO 4 ) 2 , [Mn III M n IV ( ⁇ -O) 1 (g-OAc) 2 (Me-TACN) 2 ] (ClO 4 ) 3 , [Mn IV 2 ( ⁇ -O) 3 (Me-TACN) 2 ] (PF 6 ) 2 and [Mn IV 2 ( ⁇ -O) 3 (Me / Me-TACN) 2 ] (PF 6 ) 2 (OAc
  • Machine dishwashing detergent characterized in that it is a bleaching catalyst selected from the group of bleach-enhancing transition metal salts and transition metal complexes, preferably from the group of complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me / Me-TACN) are preferred according to the invention, since the cleaning result can be significantly improved in particular by the aforementioned bleaching catalysts.
  • a bleaching catalyst selected from the group of bleach-enhancing transition metal salts and transition metal complexes, preferably from the group of complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me / Me-TACN) are preferred according to the invention, since the cleaning result can be significantly improved in particular by the aforementioned bleaching
  • the aforementioned bleach-enhancing transition metal complexes are preferably used in an amount of up to 1% by weight, in particular from 0.001% by weight to 0.1% by weight and particularly preferably from 0.01% by weight. % to 0.05 wt .-%, each based on the total weight of the agent used. In special cases, however, more bleaching catalyst can also be used.
  • the bleaching agents which can be used according to the invention are substances which are active in washing or cleaning. Among the compounds which serve as bleaching agents and supply H 2 O 2 in water, sodium percarbonate, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance. Further bleaching agents which can be used are, for example, peroxypyrophosphates, citrate perhydrates and H 2 O 2 -producing peracid 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 bleaching agents are the diacyl peroxides, such as dibenzoyl peroxide.
  • Other typical organic bleaching agents are peroxy acids, examples of which include alkyl peroxy acids and aryl peroxy acids. All other inorganic or organic peroxy bleaches known to the person skilled in the art can also be used.
  • Chlorine or bromine-releasing substances can also be used as bleaching agents.
  • Suitable materials that release chlorine or bromine include, for example, heterocyclic N-bromo- and N-chloramides, 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-dimethylhydanthoin are also suitable.
  • the bleach is in an amount of 1-35% by weight and more preferably 2-30% by weight, 3.5-25% by weight, 4-20% by weight and particularly preferably 5 -15% by weight in the dishwashing detergent according to the invention, based in each case on the total weight of the dishwashing detergent.
  • Preferred dishwashing detergents are further characterized in that the dishwashing detergent, based in each case on the total weight of the dishwashing detergent, contains 2 to 20% by weight, preferably 3 to 18% by weight and in particular 4 to 15% by weight sodium percarbonate.
  • dishwashing detergents are characterized in that the bleaching catalyst is selected from the group of the bleach-enhancing transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (methane TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me / Me-TACN), and / or the source of hydrogen peroxide is sodium percarbonate, sodium perborate tetrahydrate or sodium perborate monohydrate, or a combination thereof.
  • the bleaching catalyst is selected from the group of the bleach-enhancing transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (methane TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me / Me-TACN), and / or the source
  • the bleaching catalyst is very particularly preferably a complex of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN), in particular [Mn IV 2 ( ⁇ -O) 3 (Me-TACN) 2 ] (PF 6 ) 2 , or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me / Me-TACN) or a mixture thereof, and the hydrogen peroxide source sodium percarbonate.
  • the bleaching catalyst and the hydrogen peroxide source are preferably present in the above-mentioned amounts.
  • the automatic dishwashing detergents additionally contain at least one bleach activator.
  • Bleach activators which can be used are compounds which, under perhydrolysis conditions, give aliphatic peroxocarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • acylated multiply acylated alkylenediamines in particular tetraacetylethylene diamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT) Glycolurils, especially tetraacetylglycoluril (TAGU), N-acylimides, especially N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, especially n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS) is particularly preferably used.
  • TAED tetraacetylethylene diamine
  • DADHT 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine
  • Glycolurils especially tetraacetyl
  • TAED is very particularly preferred.
  • Combinations of conventional bleach activators can also be used. These bleach activators are preferably used in amounts of up to 10% by weight, in particular 0.1% by weight to 8% by weight, particularly 2 to 8% by weight and particularly preferably 2 to 6% by weight, in each case based on the total weight of the agent used.
  • the bleach activators can be formulated in the enzyme phase of the agent. In various embodiments, this is a preferred embodiment, which is used to separate bleach and bleach activator from one another in the agent.
  • the agents according to the invention contain at least one builder from the class of aminocarboxylic acids and their salts.
  • a particularly preferred representative of this class is methylglycinediacetic acid (MGDA) or salts thereof, but glutamine diacetic acid (GLDA) or its salts or ethylenediaminediacetic acid or its salts (EDDS) can also be used.
  • the content of these aminocarboxylic acids, in particular MGDA, or their salts can be, for example, between 5 and 35% by weight, preferably between 10 and 25% by weight and in particular between 10 and 20% by weight, in each case based on the total weight of the By means of make out.
  • Aminocarboxylic acids and their salts can be used together with other builders, in particular also with the phosphate-free builders, which are described below.
  • the agents described herein comprise at least two separate phases, namely at least one enzyme-containing phase or at least one bleach-containing phase.
  • a phase in the sense of the present invention is a spatial area in which physical parameters and the chemical composition are homogeneous.
  • One phase differs from another phase by different features, for example ingredients, physical properties, external appearance, etc.
  • Different phases can preferably be distinguished optically.
  • the at least one first phase must be clearly distinguished from the at least one second phase. If the washing or cleaning agent according to the invention has more than one first phase, these can likewise be distinguished from one another with the naked eye because they differ from one another, for example, in terms of their coloring. The same applies if there are two or more second phases. In this case, too, an optical differentiation of the phases is possible, for example on the basis of a color or transparency difference.
  • Phases in the sense of the present invention are thus self-contained areas that can be visually distinguished from one another by the consumer with the naked eye.
  • the individual phases can have different properties when used, such as speed, with which the phase dissolves in water and thus the speed and sequence of the release of the ingredients contained in the respective phase.
  • the phases are typically spatially separated from one another. In various embodiments, this can be done such that if one or both of the phases are liquid phases, the liquid phase is separate from the other phase in a separate, closed area, for example the chamber of a pouch. Such forms of confection are known in the prior art. With fixed funds, i.e. If both phases are solids, the two phases are also made up spatially separated from one another, for example in the form of a multi-chamber pouch, each of the phases being present in a separate chamber.
  • the two phases can be arranged directly adjacent to one another in such a way that the phases are formulated separately and contact each other, but cannot mix.
  • the agents according to the invention preferably contain at least one further constituent, in particular at least two further constituents, selected from the group consisting of further builders, surfactants, polymers, corrosion inhibitors and glass corrosion inhibitors, disintegration aids, fragrances and perfume carriers.
  • Additional builders can advantageously be used.
  • the additional builders that can be used include, in particular, zeolites, silicates, carbonates, organic cobuilders and - where there are no ecological prejudices against their use - phosphates.
  • the agents are preferably phosphate-free.
  • 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, Kenyait), Na-SKS-2 (Na 2 Si 14 O 29 .xH 2 O, magadiite), Na-SKS -3 (Na 2 Si 8 O 17 .xH 2 O) or Na-SKS-4 (Na 2 Si 4 O 9 .xH 2 O, makatite).
  • crystalline sheet silicates of the formula NaMSi x O 2x + 1 .yH 2 O, in which x represents 2 are particularly suitable.
  • both are ⁇ -sodium disitikate Na 2 Si 2 O 5 .y H 2 O and, above all, Na-SKS-5 ( ⁇ -Na 2 Si 2 O 5 ), Na-SKS-7 ( ⁇ -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 O 5 ) and Na-SKS-13 (NaHSi 2 O 5 ), but in particular Na-SKS-6 ( ⁇ -Na 2 Si 2 O 5 ) is preferred.
  • Automatic dishwashing detergents preferably contain from 0.1 to 20% by weight, preferably from 0.2 to 15% by weight and in particular from 0, of the crystalline layered silicate of the formula NaMSi x O 2x + 1 .yH 2 O. 4 to 10 wt .-%, each based on the total weight of these agents.
  • the delay in dissolution compared to conventional amorphous sodium silicates can be caused in various ways, for example by surface treatment, compounding, compacting / compression or by overdrying.
  • amorphous is understood to mean that the silicates in X-ray diffraction experiments do not provide sharp X-ray reflections, as are typical for crystalline substances, but at most one or more maxima of the scattered X-rays, which have a width of several degree units of the diffraction angle , cause.
  • the silicates are preferably formulated separately from the enzyme phase and, optionally, also the bleaching phase and can be contained, for example, in a third phase of the agent. Examples of such a packaging are the known solid dishwasher detergent tablets with 2 phases and a core, the core here being able to contain the silicate, for example.
  • the agents described here are preferably phosphate-free.
  • the dishwashing detergents can also contain, in particular, phosphonates as additional builders, which according to the invention are not subsumed under the phosphates.
  • a hydroxyalkane and / or aminoalkane phosphonate is preferably used as the phosphonate compound.
  • HEDP 1-hydroxyethane-1,1-diphosphonate
  • Preferred aminoalkane phosphonates are ethylenediaminetetramethylenephosphonate (EDTMP), diethylenetriaminepentamethylenephosphonate (DTPMP) and their higher homologues in question.
  • Phosphonates are contained in the detergents preferably in amounts of 0.1 to 10% by weight, in particular in amounts of 0.5 to 8% by weight, in each case based on the total weight of the dishwashing detergent.
  • the phosphonates are preferably also formulated separately from the enzyme phase, so that in various embodiments the enzyme phase contains no phosphonates.
  • the phosphonates can be formulated, for example, in the bleaching phase.
  • Alkali carriers include, for example, alkali metal hydroxides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal sesquicarbonates, the alkali silicates mentioned, alkali metal silicates, and mixtures of the abovementioned substances, the alkali metal carbonates, in particular sodium carbonate, sodium hydrogen carbonate or sodium sesquicarbonate, being preferred for the purposes of this invention.
  • a builder system containing a mixture of tripolyphosphate and sodium carbonate is particularly preferred.
  • a builder system containing a mixture of tripolyphosphate and sodium carbonate and sodium disilicate is also particularly preferred.
  • the optional alkali metal hydroxides are preferably only used in small amounts, preferably in amounts below 10% by weight, preferably below 6% by weight, particularly preferably below 4 % By weight and in particular below 2% by weight, in each case based on the total weight of the automatic dishwashing detergent.
  • alkali carriers mentioned are also preferably made up separately from the enzyme phase and can be contained, for example, in the bleaching phase.
  • organic cobuilders that may be mentioned are, in particular, polycarboxylates / polycarboxylic acids, aspartic acid, polyacetals, dextrins, other organic cobuilders and phosphonates. These classes of substances are described below.
  • Usable 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 being understood to mean those carboxylic acids which carry more than one acid function.
  • polycarboxylic acids being understood to mean those carboxylic acids which carry more than one acid function.
  • NTA nitrilotriacetic acid
  • the free acids typically also have the property of an acidifying component and thus also serve to set a lower and milder pH of the automatic dishwashing detergents.
  • Citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any mixtures thereof can be mentioned in particular.
  • automatic dishwashing agents are preferred, characterized in that the automatic dishwashing agent contains citric acid or a salt of citric acid and that the proportion by weight of citric acid or the salt of citric acid is preferably more than 5% by weight, in particular between 10 and 40% by weight. is.
  • Citric acid and citrates can also be formulated in the enzyme phase.
  • the agents according to the invention can contain surfactants, the group of surfactants including nonionic, anionic, cationic and amphoteric surfactants.
  • nonionic surfactants known to the person skilled in the art can be used as nonionic surfactants.
  • Suitable nonionic surfactants are, for example, alkyl glycosides of the general formula RO (G) x , in which R corresponds to a primary straight-chain or methyl-branched, in particular methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18, C atoms and G is the symbol is, which stands for a glycose unit with 5 or 6 carbon atoms, preferably for glucose.
  • the degree of oligomerization x which indicates the distribution of monoglycosides and oligoglycosides, is any number between 1 and 10; x is preferably 1.2 to 1.4.
  • Nonionic surfactants of the amine oxide type for example N-coconut alkyl-N, N-dimethylamine oxide and N-tallow alkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides can also be suitable.
  • the amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, in particular not more than half of them.
  • Suitable surfactants are the polyhydroxy fatty acid amides known as PHFA.
  • low-foaming nonionic surfactants are preferably used, in particular alkoxylated, especially ethoxylated, low-foaming nonionic surfactants.
  • the dishwasher detergents particularly preferably contain nonionic surfactants from the group of the alkoxylated alcohols.
  • nonionic surfactants that can be used, which can be used either as the sole nonionic surfactant or in combination with other nonionic surfactants, are accordingly alkoxylated, preferably ethoxylated or ethoxylated and propoxylated, fatty acid alkyl esters, preferably with 1 to 4 carbon atoms in the alkyl chain.
  • Preferred surfactants come from the groups of ethoxylated primary alcohols and mixtures of these surfactants with structurally more complex surfactants such as polyoxypropylene / polyoxyethylene / polyoxypropylene ((PO / EO / PO) surfactants).
  • Such (PO / EO / PO) nonionic surfactants are characterized by good foam control.
  • Suitable nonionic surfactants are those which have alternating ethylene oxide and alkylene oxide units.
  • surfactants with EO-AO-EO-AO blocks are preferred, one to ten EO or AO groups being bonded to one another before a block follows from the other groups.
  • nonionic surfactants of the general formula preferred in which R 1 represents a straight-chain or branched, saturated or mono- or polyunsaturated C 6-24 alkyl or alkenyl radical; each group R 2 or R 3 is independently selected from -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 -CH 3 , CH (CH 3 ) 2 and the indices w, x, y, z independently of one another represent integers from 1 to 6.
  • nonionic surfactants which have a C 9-15 -alkyl radical having 1 to 4 ethylene oxide units, followed by 1 to 4 propylene oxide units, followed by 1 to 4 ethylene oxide units, followed by 1 to 4 propylene oxide units.
  • Those end group-capped, poly (oxyalkylated) nonionic surfactants which, according to the formula R 1 O [CH 2 CH 2 O] ⁇ CH 2 CH (OH) R 2 , are preferred in addition to a radical R 1 which is saturated for linear or branched or unsaturated, aliphatic or aromatic hydrocarbon radicals having 2 to 30 carbon atoms, preferably having 4 to 22 carbon atoms, furthermore have a linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radical R 2 having 1 to 30 carbon atoms, where x is from 1 and 90, preferably for values between 10 and 80 and in particular for values between 20 and 60.
  • Particularly preferred are surfactants of the above formula in which R 1 is C 7 to C 13 , x is an integer from 16 to 28 and R 2 is C 8 to C 12 .
  • surfactants of the formula R 1 O [CH 2 CH (CH 3 ) O] x [CH 2 CH 2 O] y CH 2 CH (OH) R 2 , in which R 1 is a linear or branched aliphatic hydrocarbon radical with 4 up to 18 carbon atoms or mixtures thereof, R 2 denotes a linear or branched hydrocarbon radical with 2 to 26 carbon atoms or mixtures thereof and x stands for values between 0.5 and 1.5 and y stands for a value of at least 15.
  • the group of these nonionic surfactants includes, for example, the C 2-26 fatty alcohol (PO) 1 - (EO) 15-40 -2-hydroxyalkyl ethers, in particular also the C 8-10 fatty alcohol (PO) 1 - (EO) 22 -2 -hydroxydecyl ether.
  • nonionic surfactants are the end-capped poly (oxyalkylated) nonionic surfactants of the formula R 1 O [CH 2 CH (R 3 ) O] x [CH 2 ] k CH (OH) [CH 2 ] j OR 2 , in which R 1 and R 2 for linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, R 3 is H or a methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or 2 -Methyl-2-butyl radical, x stand for values between 1 and 30, k and j stand for values between 1 and 12, preferably between 1 and 5.
  • each R 3 in the above formula R 1 O [CH 2 CH (R 3 ) O] x [CH 2 ] k CH (OH) [CH 2 ] j OR 2 may be different.
  • R 1 and R 2 are preferably linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 6 to 22 carbon atoms, radicals having 8 to 18 carbon atoms being particularly preferred.
  • H, -CH 3 or -CH 2 CH 3 are particularly preferred for the radical R 3 .
  • Particularly preferred values for x are in the range from 1 to 20, in particular from 6 to 15.
  • each R 3 in the above formula can be different if x ⁇ 2.
  • the value 3 for x has been chosen here as an example and may well be larger, the range of variation increasing with increasing x values and including, for example, a large number (EO) groups combined with a small number (PO) groups, or vice versa .
  • R 1 , R 2 and R 3 are as defined above and x represents numbers from 1 to 30, preferably from 1 to 20 and in particular from 6 to 18.
  • Particularly preferred are surfactants in which the radicals R 1 and R 2 has 9 to 14 C atoms, R 3 stands for H and x assumes values from 6 to 15.
  • the group of these nonionic surfactants includes, for example, the C 4-22 fatty alcohol (EO) 10-80 -2-hydroxyalkyl ethers, in particular also the C 8-12 fatty alcohol (EO) 22 -2-hydroxydecyl ether and the C 4-22 fatty alcohol (EO) 40-80 -2-hydroxyalkyl ether.
  • the corresponding non-end-capped hydroxy mixed ethers can also be used instead of the end group-capped hydroxy mixed ethers.
  • R 2 is hydrogen and R 1 , R 3 , A, A ', A ", A"', w, x, y and z are as defined above.
  • compositions described herein which comprise at least one nonionic surfactant, preferably a nonionic surfactant from the group of hydroxy mixed ethers, contain the surfactant in various embodiments in an amount based on the total weight of the composition of at least 2% by weight, preferably at least 5% by weight. %.
  • the absolute amounts used per application can be, for example, in the range of 0.5-10 g / job, preferably in the range of 0.5-5 g / job.
  • Nonionic surfactants which have a melting point above room temperature are particularly preferred.
  • anionic surface-active substances are suitable as anionic surfactants in dishwashing detergents. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 8 to 30 carbon atoms.
  • anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 8 to 30 carbon atoms.
  • glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups can be contained in the molecule.
  • Suitable anionic surfactants are preferably in the form of the sodium, potassium and ammonium and the mono-, di- and trialkanolammonium salts with 2 to 4 carbon atoms in the alkanol group, but also zinc, manganese (II), magnesium, calcium or Mixtures of these can serve as counterions.
  • Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids with 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule.
  • cationic and / or amphoteric surfactants such as betaines or quaternary ammonium compounds can also be used. However, it is preferred that no cationic and / or amphoteric surfactants are used.
  • the agents described herein may also contain various polymers.
  • Particularly preferred unsaturated carboxylic acids are acrylic acid, methacrylic acid, ethacrylic acid, ⁇ -chloroacrylic acid, ⁇ -cyanoacrylic acid, crotonic acid, ⁇ -phenyl-acrylic acid, maleic acid, maleic anhydride, fumaric acid, itaconic acid, citraconic acid (methyl maleic acid), methylene malonic acid, sorbic acid, cinnamic acid or mixtures thereof.
  • Acrylic acid is very particularly preferred.
  • the homopolymer is therefore a polyacrylic acid.
  • the carboxylic acid groups in the polymers may be wholly or partly in neutralized form, i.e. that the acidic hydrogen atom of the carboxylic acid group in some or all of the carboxylic acid groups can be replaced by metal ions, preferably alkali metal ions and in particular by sodium ions.
  • metal ions preferably alkali metal ions and in particular by sodium ions.
  • partially or fully neutralized polymers is preferred according to the invention.
  • the molar mass of the homopolymers used can be varied in order to adapt the properties of the polymers to the desired use.
  • Preferred dishwashing detergents are characterized in that the homopolymers, in particular the polyacrylic acids, have molar masses M n of 1000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates with molecular weights from 1100 to 10000 g / mol, and particularly preferably from 1200 to 5000 g / mol, can in turn be preferred from this group.
  • the agents further contain at least one sulfopolymer.
  • the polymers which can be used in this connection are in particular copolymers which can have two, three, four or more different monomer units, at least one monomer unit carrying a sulfonic acid group.
  • preferred copolymers contain at least one monomer from the group of unsaturated carboxylic acids.
  • the unsaturated carboxylic acids described above are used with particular preference as unsaturated carboxylic acid (s).
  • Acrylic acid is very particularly preferred.
  • Particularly preferred monomers containing sulfonic acid groups are 1-acrylamido-1-propanesulfonic acid, 2-acrylamido-2-propanesulfonic acid, 2-acrylamido-2-methyl-1-propanesulfonic acid, 2-methacrylamido-2-methyl-1-propanesulfonic acid, 3- Methacrylamido-2-hydroxy-propanesulfonic acid, allylsulfonic acid, methallylsulfonic acid, allyloxybenzenesulfonic acid, methallyloxybenzenesulfonic acid, 2-hydroxy-3- (2-propenyloxy) propanesulfonic acid, 2-methyl-2-propen1-sulfonic acid, styrenesulfonic acid, vinylsulfonic acid, 3-sulfopropyl sulfopropyl acrylate , Sulfomethacrylamide, sulfomethyl methacrylamide and mixtures of the acids mentioned or their water-soluble salts.
  • the acid groups can be wholly or partly in neutralized form, i.e. that the acidic hydrogen atom of the sulfonic and / or carboxylic acid group in some or all acid groups can be exchanged for metal ions, preferably alkali metal ions and in particular for sodium ions.
  • metal ions preferably alkali metal ions and in particular for sodium ions.
  • partially or fully neutralized copolymers is preferred according to the invention.
  • the monomer distribution of the preferably used copolymers is preferably 5 to 95% by weight in each case in copolymers which contain only monomers containing carboxylic acid groups and monomers containing sulfonic acid groups, particularly preferably the proportion of the monomer containing sulfonic acid groups is 50 to 90% by weight. and the proportion of the carboxylic acid group-containing monomer 10 to 50 wt .-%, the monomers are preferably selected from the aforementioned.
  • the copolymers can contain, in addition to the above-described monomers containing carboxylic acid groups and monomers containing sulfonic acid groups, further monomers, in particular monomers containing unsaturated carboxylic acid ester groups.
  • Particularly preferred unsaturated carboxylic acid esters are alkyl esters of monocarboxylic acids such as acrylic acid, methacrylic acid, ethacrylic acid, ⁇ -chloroacrylic acid, ⁇ -cyanoacrylic acid, crotonic acid, ⁇ -phenyl-acrylic acid, sorbic acid, cinnamic acid or mixtures thereof.
  • C 1-8 alkyl esters of acrylic acid, such as methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, are very particularly preferred.
  • Ethyl acrylate is very particularly preferred.
  • the molecular weight of the copolymers used can be varied in order to adapt the properties of the polymers to the intended use.
  • Preferred dishwashing detergents are characterized in that the copolymers have molecular weights M n from 2000 to 200,000 g / mol, preferably from 4000 to 25,000 g / mol and in particular from 5000 to 15,000 g / mol.
  • the homopolymers and copolymers described above can each be used in amounts of 0.5 to 10% by weight, preferably 1 to 5% by weight, based on the total weight of the composition. Absolute amounts are typically in the range of 0.1 to 2 g / job, preferably in the range of 0.2 to 1.0 g / job.
  • the mass ratio of the polymers to one another, i.e. Homopolymer to copolymer, in various embodiments is 5: 1 to 1: 5, preferably 2: 1 to 1: 2.
  • the dishwashing detergents can alternatively or additionally contain further polymers.
  • the group of suitable polymers includes, in particular, the cleaning-active amphoteric, zwitterionic or cationic polymers, for example the rinse aid polymers and / or polymers which act as softeners.
  • Preferred amphoteric polymers that can be used come from the group of alkyl acrylamide / acrylic acid copolymers, alkyl acrylamide / methacrylic acid copolymers, alkyl acrylamide / methyl methacrylic acid copolymers, alkyl acrylamide / acrylic acid / alkylaminoalkyl (meth) acrylic acid copolymers, alkyl acrylamide / methacrylic acid / alkylaminoalkyl ( ) -acrylic acid copolymers, the alkyl acrylamide / methyl methacrylic acid / alkylaminoalkyl (meth) acrylic acid copolymers, the alkyl acrylamide / alkymethacrylate / alkylaminoethyl methacrylate / alkyl methacrylate copolymers and the copolymers of unsaturated carboxylic acids, cationically derivatized unsaturated carboxylic acids and optionally other ionic
  • zwitterionic polymers that can be used come from the group of acrylamidoalkyltrialkylammonium chloride / acrylic acid copolymers and their alkali and ammonium salts, acrylamidoalkyltrialkylammonium chloride / methacrylic acid copolymers and their alkali and ammonium salts and methacroylethylbetaine / methacrylate copolymers.
  • Cationic polymers that can be used come from the groups of the quaternized cellulose derivatives, the polysiloxanes with quaternary groups, the cationic guar derivatives, the polymeric dimethyldiallylammonium salts and their copolymers with acrylic acid and methacrylic acid and their esters and amides, the copolymers of vinylpyrrolidone with quaternylamino derivatives of quaternylamino derivatives 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.
  • Automatic dishwashing detergents preferably contain the aforementioned cationic and / or amphoteric polymers in amounts between 0.01 and 10% by weight, in each case based on the total weight of the automatic dishwashing detergent.
  • the pH of the dishwashing detergent can be adjusted using conventional pH regulators, the pH being selected depending on the intended use.
  • the pH is in a range from 5.5 to 11, preferably 5.5 to 10.5, more preferably 7 to 10.5, in particular greater than 7, especially in the range 8 to 10.
  • pH Serving agents are acids and / or alkalis, preferably alkalis.
  • Suitable acids are in particular organic acids such as acetic acid, citric acid, glycolic acid, lactic acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid or amidosulfonic acid.
  • the mineral acids hydrochloric acid, sulfuric acid and nitric acid or mixtures thereof can also be used.
  • Suitable bases come from the group of alkali and alkaline earth metal hydroxides and carbonates, in particular alkali metal hydroxides, of which potassium hydroxide and especially sodium hydroxide is preferred.
  • alkali metal hydroxides of which potassium hydroxide and especially sodium hydroxide is preferred.
  • volatile alkali is particularly preferred, for example in the form of ammonia and / or alkanolamines, which can contain up to 9 carbon atoms in the molecule.
  • the alkanolamine is preferably selected from the group consisting of mono-, di-, triethanol- and -propanolamine and mixtures thereof.
  • the agent according to the invention can also contain one or more buffer substances (INCI buffering agents), usually in amounts of 0.001 to 5% by weight. Buffer substances which are at the same time complexing agents or even chelating agents (chelators, INCI chelating agents) are preferred. Particularly preferred buffer substances are citric acid or citrates, in particular sodium and potassium citrates, for example trisodium citrate ⁇ 2H 2 O and tripotassium citrate ⁇ H 2 O.
  • Glass corrosion inhibitors prevent the appearance of cloudiness, streaks and scratches but also the iridescence of the glass surface of machine-cleaned glasses.
  • Preferred glass corrosion inhibitors come from the group of the magnesium and zinc salts and the magnesium and zinc complexes.
  • the content of zinc salt in automatic dishwashing detergents is preferably between 0.1 to 5% by weight, preferably between 0.2 to 4% by weight and in particular between 0.4 to 3% by weight or the content of zinc in oxidized form (calculated as Zn 2+ ) between 0.01 and 1% by weight, preferably between 0.02 and 0.5% by weight and in particular between 0.04 and 0.2% by weight .-%, each based on the total weight of the agent containing glass corrosion inhibitor.
  • polyethyleneimines such as are available, for example, under the name Lupasol® (BASF), preferably in an amount of 0 to 5% by weight, in particular 0.01 to 2% by weight. -%, are used as glass corrosion inhibitors.
  • fragrance compounds e.g. the synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type are used.
  • mixtures of different fragrances are preferably used, which together produce an appealing fragrance.
  • perfume oils can also contain natural fragrance mixtures as are available from plant sources, e.g. Pine, citrus, jasmine, patchouli, rose or ylang-ylang oil.
  • Preservatives can also be contained in the agents. Preservatives from the groups of alcohols, aldehydes, antimicrobial acids and / or their salts, carboxylic acid esters, acid amides, phenols, phenol derivatives, diphenyls, diphenylalkanes, urea derivatives, oxygen and nitrogen acetals and formals, benzamidines, isothiazoles and their derivatives are suitable, for example such as isothiazolines and isothiazolinones, 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 and peroxides.
  • Preferred antimicrobial agents are preferably selected from the group comprising ethanol, n-propanol, i-propanol, 1,3-butanediol, phenoxyethanol, 1,2-propylene glycol, glycerin, undecylenic acid, citric acid, lactic acid, benzoic acid, salicylic acid, Thymol, 2-benzyl-4-chlorophenol, 2,2'-methylene-bis- (6-bromo-4-chlorophenol), 2,4,4'-trichloro-2'-hydroxydiphenyl ether, N- (4-chlorophenyl) -N- (3,4-dichlorophenyl) urea, N, N '- (1,10-decanediyldi-1-pyridinyl-4-ylidene) -bis- (1-octanamine) dihydrochloride, N, N'-bis - (4-chlorophenyl) -3,12-diimino
  • particularly preferred preservatives are selected from the group comprising salicylic acid, quaternary surfactants, in particular benzalkonium chloride and isothiazoles and their derivatives such as isothiazolines and isothiazolinones.
  • the machine dishwashing detergents described here can be assembled in different ways.
  • the agents can be in solid or liquid as well as a combination of solid and liquid supply forms.
  • powders, granules, extrudates, compactates, in particular tablets are suitable as fixed supply forms.
  • the liquid supply forms based on water and / or organic solvents can be thickened, in the form of gels.
  • the agents are packaged in the form of multi-phase products. The individual phases of such multiphase agents can have the same or different physical states.
  • the dishwashing detergents can be in the form of moldings.
  • disintegration aids so-called tablet disintegrants
  • Tablet disintegrants or accelerators of disintegration are understood to mean auxiliary substances which ensure the rapid disintegration of tablets in water or other media and the rapid release of the active substances.
  • Disintegration aids can preferably be used in amounts of 0.5 to 10% by weight, preferably 3 to 7% by weight and in particular 4 to 6% by weight, in each case based on the total weight of the agent containing disintegration aids.
  • the automatic dishwashing agents described herein are preferably prefabricated into dosing units. These dosing units are then also packaged as multi-phase products and preferably comprise the amount of cleaning-active substances necessary for a cleaning cycle. Preferred dosing units have a weight between 12 and 30 g, preferably between 14 and 26 g and in particular between 15 and 22 g.
  • the volume of the aforementioned dosing units and their spatial shape are selected with particular preference such that the pre-assembled units can be dosed via the dosing chamber of a dishwasher.
  • the volume of the dosing unit is therefore preferably between 10 and 35 ml, preferably between 12 and 30 ml.
  • the machine dishwashing detergents in particular the prefabricated metering units, particularly preferably have a water-soluble coating.
  • the water-soluble covering is preferably formed from a water-soluble film material which is selected from the group consisting of polymers or polymer mixtures.
  • the sheath can be formed from one or two or more layers of the water-soluble film material.
  • the water-soluble film material of the first layer and the further layers, if present, can be the same or different. Films which, for example, can be glued and / or sealed to form packaging, such as hoses or pillows, are particularly preferred after they have been filled with an agent.
  • the water-soluble packaging can have one or more chambers.
  • the agent may be contained in one or more compartments, if any, of the water-soluble envelope.
  • the amount of agent preferably corresponds to the full or half dose required for a rinse cycle.
  • the water-soluble envelope contain polyvinyl alcohol or a polyvinyl alcohol copolymer.
  • Water-soluble coatings which contain polyvinyl alcohol or a polyvinyl alcohol copolymer have good stability with a sufficiently high water solubility, in particular cold water solubility.
  • Suitable water-soluble films for producing the water-soluble covering are preferably based on a polyvinyl alcohol or a polyvinyl alcohol copolymer, the molecular weight of which is in the range from 5,000 to 1,000,000 gmol -1 , preferably from 20,000 to 500,000 gmol -1 , particularly preferably from 30,000 to 100,000 gmol -1 and is in particular from 40,000 to 80,000 gmol -1 .
  • Polyvinyl alcohol is usually produced by hydrolysis of polyvinyl acetate, since the direct route of synthesis is not possible. The same applies to polyvinyl alcohol copolymers which are produced from polyvinyl acetate copolymers accordingly. It is preferred if at least one layer of the water-soluble coating comprises a polyvinyl alcohol, the degree of hydrolysis of which is 70 to 100 mol%, preferably 80 to 90 mol%, particularly preferably 81 to 89 mol% and in particular 82 to 88 mol%.
  • a polymer material containing polyvinyl alcohol which is suitable for producing the water-soluble covering can additionally be a polymer selected from the group comprising (meth) acrylic acid-containing (co) polymers, polyacrylamides, oxazoline polymers, polystyrene sulfonates, polyurethanes, polyesters, polyethers, polylactic acid or mixtures of the above Polymers can be added.
  • a preferred additional polymer is polylactic acid.
  • preferred polyvinyl alcohol copolymers comprise dicarboxylic acids as further monomers.
  • Suitable dicarboxylic acids are itaconic acid, malonic acid, succinic acid and mixtures thereof, itaconic acid being preferred.
  • polyvinyl alcohol copolymers include, in addition to vinyl alcohol, an ethylenically unsaturated carboxylic acid, its salt or its ester.
  • Such polyvinyl alcohol copolymers particularly preferably contain, in addition to vinyl alcohol, acrylic acid, methacrylic acid, acrylic acid ester, methacrylic acid ester or mixtures thereof.
  • the film material contains further additives.
  • the film material can contain, for example, plasticizers such as dipropylene glycol, ethylene glycol, diethylene glycol, propylene glycol, glycerin, sorbitol, mannitol or mixtures thereof.
  • Other additives include, for example, release aids, fillers, crosslinking agents, surfactants, antioxidants, UV absorbers, antiblocking agents, anti-adhesive agents or mixtures thereof.
  • Suitable water-soluble films for use in the water-soluble wrappings of the water-soluble packaging according to the invention are films which are sold by MonoSol LLC, for example under the name M8630, C8400 or M8900.
  • Other suitable films include films with the designation Solublon® PT, Solublon® GA, Solublon® KC or Solublon® KL from Aicello Chemical Europe GmbH or the films VF-HP from Kuraray.
  • the multi-phase dishwashing detergent is closely enveloped by a water-soluble film
  • the water-soluble film which is preferably used in the narrow wrapping, particularly preferably comprises polyvinyl alcohol, as described above, the starting thickness preferably being from 10 ⁇ m to 100 ⁇ m, in particular from 12 ⁇ m to 60 ⁇ m, particularly preferably from 15 ⁇ m to 50 ⁇ m, especially from 20 ⁇ m to 40 ⁇ m, in particular from 22 ⁇ m to 35 ⁇ m is used.
  • the mechanism described here will not work if the casing is not snug, since the tablet can swell without the casing being blown up.
  • the use of a swellable disintegration agent is superior to a gas-generating system, since its explosive effect in any case leads to the casing being torn open. In a gas-generating system, the explosive effect can "dissipate" by the gas escaping from a leak in the casing.
  • Preferred detergent or cleaning agent disposable portions according to the invention are characterized in that the distance between the single portion and water-soluble coating over the entire area is 0.1 to 1000 ⁇ m, preferably 0.5 to 500 ⁇ m, particularly preferably 1 to 250 ⁇ m and in particular 2.5 to 100 ⁇ m.
  • the film covering is first loosely placed around a single detergent or cleaning agent portion and welded and then shrunk onto it, so that there is close contact between the film packaging and the cleaning agent concentrate.
  • disposable detergent or cleaning agent portions according to the invention are characterized in that the wrapper is a film packaging shrunk onto it.
  • this wrapping can be carried out by placing a water-soluble bottom film on a transport chain or a mold (s), then placing one or more detergent or cleaning agent portions (s) on the bottom film; then a water-soluble top film is placed on the detergent or cleaning agent portion (s) on the bottom film and this is then fixed on the bottom film, including the detergent or cleaning agent portion (s),
  • this step can also be carried out using a single-strand film, which is then placed around the one-time portions as a tube.
  • the foils are then sealed and optionally cut.
  • the film can then be shrink-wrapped using hot air or infrared radiation, optionally with pressure.
  • Exemplary formulations of the agents according to the invention in particular also include phosphate-free dishwashing agents.
  • An exemplary recipe in which those described herein Polymers can be used as additional components in the specified amounts the following is: Phosphate-free, solid dishwashing detergent formulation (tab): raw material Quantity (% by weight) Na citrate 15.00-20.00 Phosphonate (e.g.
  • the corresponding use of the automatic dishwashing agents according to the invention is also an object of the invention.
  • the invention also relates to a dishwashing method, in particular machine dishwashing method, in which a dishwashing agent according to the invention is used.
  • the subject of the present application is therefore also a method for cleaning dishes in a dishwasher, in which the agent according to the invention is metered into the interior of a dishwasher during the course of a dishwasher program before the start of the main wash cycle or in the course of the main wash cycle.
  • the metering or entry of the invention By means of the interior of the dishwasher can be done manually, but the agent is preferably dosed into the interior of the dishwasher by means of the dosing chamber.
  • the cleaning performance was determined in Miele GSL dishwashers in the 45 ° C program. Water hardness 21 ° dH. For this, 20 g of the above recipes (tab) were used. At the end of the wash cycle, the dishes were visually checked on a scale of 1-10. The higher the value, the better the cleaning performance. It can be seen that the formulation E1 according to the invention, which contains MGDA in the bleaching phase, shows a better cleaning performance on enzyme-sensitive soiling, such as minced meat, compared to the comparison formulation V1, which contains MGDA in the enzyme phase (Table 2). Table 2: Cleaning performance ADW product (fresh) Minced meat E1 6.3 V1 5.9 ADW product After 1 week storage at 40 ° C E1 6.6 V1 5.9

Landscapes

  • 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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Claims (10)

  1. Détergent pour lave-vaisselle, caractérisé en ce que le détergent pour lave-vaisselle comprend :
    (A) une phase enzymatique, la phase enzymatique contenant au moins une enzyme et étant sensiblement exempte d'agents de blanchiment et d'adjuvants organiques de la classe des acides aminocarboxyliques et de leurs sels ; et
    (B) une phase de blanchiment, la phase de blanchiment contenant au moins un agent de blanchiment, au moins un catalyseur de blanchiment et au moins un adjuvant organique de la classe des acides aminocarboxyliques et leurs sels, notamment l'acide méthylglycinediacétique (MGDA) ou ses sels.
  2. Détergent pour lave-vaisselle selon la revendication 1, caractérisé en ce que l'au moins une enzyme comprend au moins une protéase et de préférence également au moins une amylase.
  3. Détergent pour lave-vaisselle selon la revendication 1 ou 2, caractérisé en ce que le catalyseur de blanchiment est choisi dans le groupe des sels de métaux de transition améliorant le blanchiment et des complexes de métaux de transition, de préférence des complexes de manganèse à l'étape d'oxydation II, III, IV ou IV, qui contiennent un ou plusieurs ligands macrocycliques avec les fonctions donneurs N, NR, PR, O et/ou S, de manière particulièrement préférée qui contiennent les ligands macromoléculaires 1,4,7-triméthyl-1,4,7-triazacyclononane (Me-TACN), 1, 4,7-triazacyclononane (TACN), 1,5,9-triméthyl-1,5,9-triazacyclododécane (Me-TACD), 2-méthyl-1,4,7-triméthyl-1,4,7-triazacyclononane (Me/Me-TACN) et/ou 2-méthyl-1,4,7-triazacyclononane (Me/TACN), de manière préférée entre toutes les ligands 1,4,7-triméthyl-1,4,7-triazacyclononane (Me-TACN) ou 1,2,4,7-tétraméthyl-1,4,7-triazacyclononane (Me/Me-TACN).
  4. Détergent pour lave-vaisselle selon l'une des revendications 1 à 3, caractérisé en ce que le catalyseur de blanchiment est contenu dans une quantité de 0,001 à 0,1 % en poids, de préférence de 0,01 à 0,05 % en poids, par rapport au poids total du détergent pour lave-vaisselle.
  5. Détergent pour lave-vaisselle selon l'une des revendications 1 à 4, caractérisé en ce que
    (1) l'au moins un agent de blanchiment est choisi dans le groupe constitué du percarbonate de sodium, du perborate de sodium tétrahydraté, du perborate de sodium monohydraté, des peroxypyrophosphates, des citrate perhydrates, des perbenzoates, des peroxophtalates, de l'acide dipérazélaïque, du phtaloiminoperacide, de l'acide diperdodécanedioïque, du peroxyde de diacyle, de l'acide alkylperoxy et de l'acide arylperoxy, de préférence parmi le percarbonate de sodium, le perborate de sodium tétrahydraté et le perborate de sodium monohydraté, de manière davantage préférée le percarbonate de sodium ; et/ou
    (2) l'au moins un agent de blanchiment est contenu dans une quantité de 1 à 35 % en poids et de manière davantage préférée de 2 à 30 % en poids, de 3,5 à 25 % en poids, de 4 à 20 % en poids, et de manière particulièrement préférée, de 5 à 15 % en poids, dans le détergent pour vaisselle, dans chaque cas par rapport au poids total du détergent pour vaisselle.
  6. Détergent pour lave-vaisselle selon l'une des revendications 1 à 5, caractérisé en ce que l'au moins un adjuvant organique est le MGDA, et la phase enzymatique est sensiblement exempte de MGDA.
  7. Détergent pour lave-vaisselle selon l'une des revendications 1 à 6, caractérisé en ce que l'au moins un adjuvant organique de la classe des acides aminocarboxyliques et leurs sels est contenu en une quantité de 5 à 35 % en poids, de préférence de 10 à 25 % en poids, et en particulier de 10 à 20 % en poids, par rapport au poids du détergent total, dans le détergent pour vaisselle.
  8. Détergent pour lave-vaisselle selon l'une des revendications 1 à 7, caractérisé en ce que
    (1) le détergent pour lave-vaisselle se présente sous forme solide ; et/ou
    (2) le détergent pour lave-vaisselle se présente sous forme pré-portionnée ; et/ou
    (3) les phases d'enzyme et de blanchiment sont séparées dans l'espace ; et/ou
    (4) le détergent pour lave-vaisselle contient au moins un activateur de blanchiment, en particulier dans la phase enzymatique ; et/ou
    (5) le détergent pour lave-vaisselle contient au moins un autre constituant, de préférence au moins deux autres constituants, choisis dans le groupe constitué d'autres adjuvants, de tensioactifs, de polymères, d'inhibiteurs de corrosion, d'inhibiteurs de corrosion du verre, d'auxiliaires de désintégration, de parfums et de supports de parfum.
  9. Utilisation d'un détergent pour lave-vaisselle selon l'une des revendications 1 à 8 dans un procédé de lavage automatique de vaisselle.
  10. Procédé de lavage automatique de vaisselle, caractérisé en ce qu'un détergent pour lave-vaisselle est utilisé selon l'une des revendications 1 à 8.
EP16741307.9A 2015-07-23 2016-07-20 Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes Active EP3325597B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL16741307T PL3325597T3 (pl) 2015-07-23 2016-07-20 Środek do maszynowego mycia naczyń zawierający środki wybielające, wypełniacze aktywne i enzymy

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102015213940.9A DE102015213940A1 (de) 2015-07-23 2015-07-23 Maschinelles Geschirrspülmittel enthaltend Bleichmittel, Builder und Enzyme
PCT/EP2016/067263 WO2017013159A1 (fr) 2015-07-23 2016-07-20 Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes

Publications (2)

Publication Number Publication Date
EP3325597A1 EP3325597A1 (fr) 2018-05-30
EP3325597B1 true EP3325597B1 (fr) 2020-07-01

Family

ID=56497769

Family Applications (1)

Application Number Title Priority Date Filing Date
EP16741307.9A Active EP3325597B1 (fr) 2015-07-23 2016-07-20 Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes

Country Status (5)

Country Link
EP (1) EP3325597B1 (fr)
DE (1) DE102015213940A1 (fr)
ES (1) ES2810750T3 (fr)
PL (1) PL3325597T3 (fr)
WO (1) WO2017013159A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4379028A1 (fr) * 2022-11-30 2024-06-05 Henkel AG & Co. KGaA Systeme de builder pour l'élimination des taches de protéines

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102017212561A1 (de) * 2017-07-21 2019-01-24 Henkel Ag & Co. Kgaa Geschirrspülmittel enthaltend Citratdihydrat und -anhydrat
CA3081788C (fr) 2017-11-14 2022-08-09 Ecolab Usa Inc. Compositions detergentes caustiques a liberation controlee de matieres solides
CN114222808A (zh) 2019-09-27 2022-03-22 埃科莱布美国股份有限公司 浓缩二合一洗碗机洗涤剂和漂洗助剂

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100292120A1 (en) 2007-09-28 2010-11-18 Reckitt Benckiser N.V Detergent Composition
WO2012025740A1 (fr) 2010-08-27 2012-03-01 Reckitt Benckiser N.V. Composition de détergent comprenant de l'oxalate de manganèse
US20140018278A1 (en) 2012-07-11 2014-01-16 Xinbei Song Dishwashing composition with improved protection against aluminum corrosion
WO2014100100A1 (fr) 2012-12-20 2014-06-26 The Procter & Gamble Company Composition de détergent ayant un agent de blanchiment revêtu par du silicate
WO2014099854A1 (fr) 2012-12-21 2014-06-26 The Procter & Gamble Company Système de nettoyage
WO2015051896A1 (fr) 2013-10-07 2015-04-16 Weylchem Wiesbaden Gmbh Poche à plusieurs compartiments comprenant des compositions de nettoyage, procédé de lavage et utilisation pour le lavage et le nettoyage de textiles et de vaisselle

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10245262A1 (de) 2002-05-24 2004-04-08 Henkel Kgaa Einspülkammer-dosierbare Tabletten-Portionen II
DE10245260A1 (de) 2002-09-27 2004-04-15 Henkel Kgaa Verfahren zur Herstellung umhüllter Wasch- oder Reinigungsmittel-Portionen
DE102013225485A1 (de) * 2013-12-10 2015-06-11 Henkel Ag & Co. Kgaa Reinigungskraftverstärker für maschinelle Geschirrspülmittel

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100292120A1 (en) 2007-09-28 2010-11-18 Reckitt Benckiser N.V Detergent Composition
WO2012025740A1 (fr) 2010-08-27 2012-03-01 Reckitt Benckiser N.V. Composition de détergent comprenant de l'oxalate de manganèse
US20140018278A1 (en) 2012-07-11 2014-01-16 Xinbei Song Dishwashing composition with improved protection against aluminum corrosion
WO2014100100A1 (fr) 2012-12-20 2014-06-26 The Procter & Gamble Company Composition de détergent ayant un agent de blanchiment revêtu par du silicate
WO2014099854A1 (fr) 2012-12-21 2014-06-26 The Procter & Gamble Company Système de nettoyage
WO2015051896A1 (fr) 2013-10-07 2015-04-16 Weylchem Wiesbaden Gmbh Poche à plusieurs compartiments comprenant des compositions de nettoyage, procédé de lavage et utilisation pour le lavage et le nettoyage de textiles et de vaisselle

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4379028A1 (fr) * 2022-11-30 2024-06-05 Henkel AG & Co. KGaA Systeme de builder pour l'élimination des taches de protéines

Also Published As

Publication number Publication date
DE102015213940A1 (de) 2017-01-26
ES2810750T3 (es) 2021-03-09
PL3325597T3 (pl) 2020-12-28
WO2017013159A1 (fr) 2017-01-26
EP3325597A1 (fr) 2018-05-30

Similar Documents

Publication Publication Date Title
EP3325596B1 (fr) Lessive lave-vaisselle contenant des agents de blanchiment et des polymères
EP3209762B1 (fr) Détergent pour lave-vaisselle contenant des complexes métalliques
EP2220205A1 (fr) Produit de nettoyage
EP3325592B1 (fr) Utilisation d'une combinaison d'un agent complexant et d'un tensioactif pour améliorer l'efficacité de rinçage
DE102007059968A1 (de) Reinigungsmittel
EP3325597B1 (fr) Lessive lave-vaisselle contenant des agents de blanchiment et des enzymes
EP3325591B1 (fr) Produit pour lave-vaisselle multiphase à noyau tensioactif
EP3431575B1 (fr) Détergent pour lave-vaisselle comportant un citrate dihydraté et anhydre
EP3481936B1 (fr) Produit vaisselle contenant de l'ose acide et de l'acide aminocarboxylique
EP3502224A1 (fr) Détergent pour lave-vaisselle à performance de nettoyage améliorée, procédé reposant sur l'utilisation dudit détergent ainsi que l'utilisation dudit détergeant
WO2015086475A1 (fr) Lessive lave-vaisselle contenant des agents complexants à base de n
EP4008764A1 (fr) Nettoyage amélioré au moyen du carbonate d'hydrogène dans le détergent de lavage en machine
DE102018212086A1 (de) Geschirrspülmittel mit Ceteareth-9
EP3078732A1 (fr) Produit de rinçage pour lave vaisselle comprenant des complexants a base d'azote et mgda
DE102017212348A1 (de) Verwendung eines Reinigungsmittels enthaltend Aminocarbonsäuren und Sulfopolymere zur Belagsinhibierung
DE102013226440A1 (de) Maschinelles Geschirrspülmittel enthaltend Emulgatoren
EP3839024A1 (fr) Système de principe actif contre la formation de taches de calcaire
EP3842511A1 (fr) Tensioactif non ionique permettant d'améliorer l'efficacité de rinçage en lavage de vaisselle automatique
DE102017223120A1 (de) Maschinelles Geschirrspülmittel mit verbesserter Reinigungsleistung, Verfahren unter Einsatz dieses Mittels sowie Verwendung des Mittels
DE102020214069A1 (de) Metallkomplexe und Geschirrspülmittel, die sie enthalten
DE102021214708A1 (de) Metallkomplexe und Geschirrspülmittel, die sie enthalten
DE102020214114A1 (de) Metallkomplexe und Geschirrspülmittel, die sie enthalten
EP3502220A1 (fr) Détergent pour lave-vaisselle à performance de rinçage et de nettoyage améliorée, procédé reposant sur l'utilisation dudit détergent ainsi que l'utilisation dudit détergent
EP3498810A1 (fr) Détergent pour lave-vaisselle à performance de rinçage et de nettoyage améliorée, procédé reposant sur l'utilisation dudit détergent ainsi que l'utilisation dudit détergent
WO2018002178A1 (fr) Détergent permettant de réduire la corrosion du verre

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20180110

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20190319

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20200220

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1286196

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200715

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502016010386

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201001

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20200701

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201001

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201002

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201102

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201101

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2810750

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20210309

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 502016010386

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

26 Opposition filed

Opponent name: RECKITT BENCKISER FINISH B.V.

Effective date: 20210312

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20200731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200731

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200731

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200720

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200731

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

R26 Opposition filed (corrected)

Opponent name: RECKITT BENCKISER FINISH B.V.

Effective date: 20210312

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200720

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200701

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 1286196

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210720

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210720

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230705

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20230724

Year of fee payment: 8

Ref country code: ES

Payment date: 20230926

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20230707

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240719

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240725

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240730

Year of fee payment: 9