EP1141211B1 - Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides - Google Patents

Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides Download PDF

Info

Publication number
EP1141211B1
EP1141211B1 EP99962240A EP99962240A EP1141211B1 EP 1141211 B1 EP1141211 B1 EP 1141211B1 EP 99962240 A EP99962240 A EP 99962240A EP 99962240 A EP99962240 A EP 99962240A EP 1141211 B1 EP1141211 B1 EP 1141211B1
Authority
EP
European Patent Office
Prior art keywords
weight
bleach
formula
compound
compounds
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.)
Expired - Lifetime
Application number
EP99962240A
Other languages
German (de)
English (en)
Other versions
EP1141211A2 (fr
Inventor
Christian Nitsch
Horst-Dieter Speckmann
Jürgen Härer
Andreas Lietzmann
Susan P. Huestis
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
Priority claimed from DE19857596A external-priority patent/DE19857596A1/de
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP1141211A2 publication Critical patent/EP1141211A2/fr
Application granted granted Critical
Publication of EP1141211B1 publication Critical patent/EP1141211B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905—Bleach activators or bleach catalysts
    • C11D3/3907—Organic compounds
    • C11D3/3917—Nitrogen-containing compounds
    • C11D3/3927—Quarternary ammonium compounds
    • 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
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905—Bleach activators or bleach catalysts
    • C11D3/3935—Bleach activators or bleach catalysts granulated, coated or protected
    • 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
    • C11D17/0034—Fixed on a solid conventional detergent ingredient
    • 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
    • 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/046—Salts
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • 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
    • C11D3/168—Organometallic compounds or orgometallic complexes
    • 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
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905—Bleach activators or bleach catalysts
    • C11D3/3907—Organic compounds
    • C11D3/3917—Nitrogen-containing compounds
    • C11D3/3925—Nitriles; Isocyanates or quarternary ammonium nitriles

Definitions

  • the present invention relates to the use of ready-made particles Acetonitrile derivatives as activators for in particular inorganic peroxygen compounds for bleaching tea stains on dishes and cleaning agents for dishes containing such activators.
  • Inorganic peroxygen compounds especially hydrogen peroxide and solid peroxygen compounds, which dissolve in water to release hydrogen peroxide, such as sodium perborate and sodium carbonate perhydrate, have long been used as oxidizing agents for disinfection and bleaching purposes.
  • the oxidizing effect of these substances in dilute solutions depends strongly on the temperature; For example, with H 2 O 2 or perborate in alkaline bleaching liquors, sufficiently quick bleaching of soiled textiles can only be achieved at temperatures above about 80 ° C.
  • the oxidation effect of the inorganic peroxygen compounds can be improved by the addition of so-called bleach activators, for which numerous suggestions, especially from the substance classes of the N- or O-acyl compounds, for example multiply acylated alkylenediamines, in particular tetraacetylethylenediamine, acylated glycolurils, in particular tetraacetylglycoluril, N- acylated hydantoins, hydrazides, triazoles, Hydrotriazine, urazoles, diketopiperazines, sulfuryl amides and cyanurates, also carboxylic anhydrides, especially phthalic anhydride, Carbonklareester, especially sodium nonanoyloxybenzenesulfonate, sodium isononanoyloxybenzenesulfonate and acylated sugar derivatives, such as pentaacetylglucose, are known in the literature.
  • the bleach activators for which numerous suggestions
  • Another one especially for cleaning agents for automatic dishwashing is the need to use corrosion inhibitors for silverware in such agents to incorporate, especially if the agents are the bleaching or Contain oxidizing agents based on oxygen.
  • Silver can when cleaning with sulfur-containing substances that are dissolved or dispersed in the rinse water are reacting, because when cleaning dishes in household dishwashers are leftovers and, among other things, mustard, peas, egg and others sulfur-containing compounds such as mercaptoamino acids introduced into the washing liquor.
  • the much higher temperatures during machine washing and the longer ones Contact times with the sulfur-containing food residues favor compared to manual flushing tarnishing silver. Due to the intensive cleaning process in the dishwasher also completely degreases the silver surface and thereby more sensitive to chemical influences.
  • tarnishing silver becomes particularly acute if it is an alternative to the Sulfur-containing substances oxidatively "defusing" active chlorine compounds active oxygen compounds, such as sodium perborate or sodium percarbonate are used, which for the removal, bleachable stains, such as for example tea stains / tea deposits, coffee residues, dyes from vegetables, lipstick residues and the like serve.
  • active chlorine compounds such as sodium perborate or sodium percarbonate are used, which for the removal, bleachable stains, such as for example tea stains / tea deposits, coffee residues, dyes from vegetables, lipstick residues and the like serve.
  • Such active oxygen bleaching agents are usually used together with bleach activators used in automatic dishwashing detergents.
  • These funds generally consist of the following function blocks: builder component (complexing agent / dispersant), Alkali carrier, bleaching system (combination of bleach and bleach activator), Enzyme and surfactant.
  • builder component complexing agent / dispersant
  • Alkali carrier Alkali carrier
  • bleaching system combination of bleach and bleach activator
  • Enzyme and surfactant Among those that occur when using such structured means Flushing conditions generally not only form sulfidic, but also but through the oxidizing attack of the intermediate peroxides or the active oxygen also oxidic deposits on the silver surfaces.
  • a subclass of the particulate agents are cleaning agents in tablet form.
  • Tableted detergents have compared to powdered or liquid products A number of advantages: They are easier to dose and to handle due to its compact structure, advantages in storage and transport. It there is therefore an extremely broad state of the art in washing and Detergent tablets, which can also be found in an extensive patent literature reflected.
  • the developers of tablet-shaped products came up with the idea early on come determined over differently composed areas of the molded body Ingredients only under defined conditions in the washing or cleaning cycle release, in order to improve the cleaning success.
  • the Core / shell tablets and ring / core tablets well known from pharmacy in particular multilayered molded articles, which are used today for many Areas of washing and cleaning or hygiene are offered.
  • Multi-phase cleaning tablets for the toilet are used, for example, in Europe Patent application EP 0 055 100 described.
  • This document discloses blocks of toilet detergent, which is a molded body made from a slowly soluble detergent composition include in which a bleach tablet is embedded. This font at the same time reveals the most diverse forms of design in a multi-phase manner Formgroiper.
  • the molded articles are produced according to the teaching of this document either by inserting a compressed bleach tablet into a mold and Pour this tablet around with the detergent composition, or by Pour some of the detergent composition into the mold, followed by the Insert the compressed bleach tablet and possibly pour it over with another detergent composition.
  • European patent application EP 0 481 547 also describes multi-phase detergent tablets, those according to this document for machine dishwashing should be used. These tablets have the shape of core / shell tablets and are produced by gradually compressing the components: Compression of a bleaching agent composition into a shaped body which is incorporated in a a polymer composition half-filled die is inserted, which then with filled up another polymer composition and one with a polymer jacket provided bleach molding is pressed. The procedure is then followed by an alkaline detergent composition repeated so that a three-phase molded body results.
  • N-alkyl ammonium nitriles of the type described above by formula (I) known in granular form have been assembled, with the support materials for the N-alkyl-ammonium nitriles for example called silica, silicates and aluminum oxide become.
  • N-alkyl ammonium nitriles that have been made up in granular form are, for example, as carrier materials for the N-alkyl ammonium nitriles Silicic acid, silicates and aluminum oxide can be called.
  • the invention relates to the use of compounds of the general formula I which are made up in particulate form with the aid of inorganic carrier materials which contain silicon R 1 R 2 R 3 N + CH 2 CN X - in which R 1 , R 2 and R 3 are, independently of one another, an alkyl, alkenyl or aryl group having 1 to 18 C atoms, the groups R 2 and R 3 also being part of a heterocycle which includes the N atom and optionally further hetero atoms and X is a charge-balancing anion, as activators for in particular inorganic peroxygen compounds in solid cleaning agents, in particular for dishes, which are used in essentially aqueous cleaning solutions.
  • R 1 is preferably an alkyl group with 1 to 3 carbon atoms, in particular a methyl group.
  • the anions X - include in particular the halides such as chloride, fluoride, iodide and bromide, nitrate, hydroxide, hexafluorophosphate, sulfate, hydrogen sulfate, methosulfate and ethosulfate, chlorate, perchlorate, and the anions of carboxylic acids such as formate, acetate, benzoate or citrate , Preference is given to the use of compounds of the formula I in which X is sulfate, hydrogen sulfate or methosulfate.
  • the compound according to general formula I is in the cleaning agents in Particulate form, that is applied to an inorganic Carrier material used.
  • the application to the carrier material can be done in this way happen that one in an aqueous solution, the compound according to formula I, as in In the context of their manufacture, the carrier material is stirred in and the aqueous Solvent is removed in vacuo, if appropriate at elevated temperature.
  • the silicon-containing inorganic carrier materials such are preferably used whose inner surface area ranging from 10 m 2 / g to 500 m 2 / g, more preferably 100m 2 / g to 450 m 2 / g is.
  • Silicates, silicas, silica gels and clays and mixtures thereof are suitable, for example.
  • the carrier material is preferably free of zeolites.
  • Silicas that have been produced using a thermal process can be used as well as silicas produced by wet processes.
  • Silica gels are colloidal silicas with elastic to solid consistency and a largely loose pore structure, which results in a high fluid absorption capacity They can be produced by the action of mineral acids on water glass Clays are naturally occurring crystalline or amorphous silicates of aluminum, iron, magnesium, calcium, potassium and sodium, for example kaolin, talc, pyrophyllite, attapulgite, sepiolite, montmorillionite and bauxite
  • the use of aluminum silicate as a carrier material or as a component of a carrier material mixture is possible, and the carrier material preferably has particle sizes in the range from 100 ⁇ m to 1.5 mm.
  • the particulate compounds of formula I are preferably 10 to 50 parts by weight of the silicon-containing carrier material and 50 to 90 parts by weight the compound of formula I.
  • the particulate made with the support material containing silicon Acetonitrile derivative can additionally be an organic material with a melting point above 40 ° C, especially non-ionic surfactant and / or with such to be enveloped. This can reduce the decay properties of the corresponding particle in affect aqueous systems and / or its storage stability positively.
  • An acetonitrile derivative according to formula I which is made up in this way in particulate form preferably incorporated into cleaning agents for use in cleaning solutions are provided for dishes for bleaching colored stains.
  • bleaching means both bleaching on its own Dish dirt, especially tea, as well as the bleaching of dirt detached from the surface of the dishwashing liquid Roger that.
  • the invention relates to solid cleaning agents for dishes and among them preferably those for use in machine cleaning processes, the one above Compound according to formula I described in a corresponding particulate Knfetation ist included, and a process for cleaning dishes using such a compound.
  • the use according to the invention as a bleach activator essentially consists in Presence of a dish surface contaminated with colored stains to create, among which a peroxidic oxidizing agent and the bleach activating Acetonitrile derivative can react with each other, with the aim of stronger to obtain oxidizing secondary products.
  • a peroxidic oxidizing agent and the bleach activating Acetonitrile derivative can react with each other, with the aim of stronger to obtain oxidizing secondary products.
  • Such conditions lie in particular then when both reactants meet in aqueous solution. This can by separately adding the peroxygen compound and the acetonitrile derivative to one if necessary, detergent-containing solution.
  • an inventive Dishwashing detergent containing the bleach activating acetonitrile derivative and optionally an oxidizing agent containing peroxygen preferably selected from the group includes organic peracids, hydrogen peroxide, perborate and percarbonate as well as their mixtures.
  • the peroxygen compound can also separately, in bulk or as a preferably aqueous solution or suspension for Solution can be added if a peroxide-free cleaning agent is used.
  • the conditions can be varied widely depending on the intended use. So come in addition to purely aqueous solutions, also mixtures of water and suitable organic solutions Solvents as a reaction medium in question.
  • the quantities of peroxygen compounds used are generally chosen so that in the solutions between 10 ppm and 10% active oxygen, preferably between 50 ppm and 5,000 ppm Active oxygen is present.
  • the amount of bleach activating used Acetonitrile derivative depends on the application. Depending on the desired degree of activation become 0.00001 mol to 0.25 mol, preferably 0.001 mol to 0.02 mol activator per mole of peroxygen compound used, but in special cases these limits are also exceeded or fallen below.
  • Another object of the invention is a solid detergent for dishes, which 1 wt .-% to 10 wt .-%, in particular 2 wt .-% to 6 wt .-% of a Acetonitrile derivative according to formula I in particulate as described above Assembled form in addition to usual ingredients compatible with the compound contains.
  • the solid cleaning agents according to the invention which are in powder or tablet form Solids, homogeneous solutions or suspensions can also be present Bleach activator used according to the invention in principle all known and in such Contain common ingredients.
  • the agents according to the invention can in particular builder substances, surface-active surfactants, peroxygen compounds, water-miscible organic solvents, enzymes, sequestering agents, electrolytes, pH regulators and other auxiliaries, such as silver corrosion inhibitors, foam regulators, contain additional bleach-boosting active ingredients as well as colors and fragrances.
  • a cleaning agent according to the invention can also have an abrasive effect Components, in particular from the group comprising quartz flours, wood flours, Plastic flours, chalks and micro glass balls and their mixtures.
  • Abrasives are preferably not present in the cleaning agents according to the invention 20 wt .-%, in particular from 5 wt .-% to 15 wt .-%, contain.
  • Another object of the invention is a means for machine cleaning Tableware containing 15% by weight to 70% by weight, in particular 20% by weight to 60% by weight water-soluble builder component, 5% by weight to 25% by weight, in particular 8% by weight up to 17% by weight of bleaching agent based on oxygen, in each case based on the total agent, which is a bleach activating acetonitrile derivative according to formula I, especially in Amounts from 2% to 6% by weight in particulate as described above contains form.
  • Such an agent is in a preferred embodiment lower alkaline, i.e. its 1% by weight solution has a pH value from 8 to 11.5, in particular from 9 to 11.
  • alkali phosphates which in Form of their alkaline neutral or acidic sodium or potassium salts can.
  • alkali phosphates which in Form of their alkaline neutral or acidic sodium or potassium salts can.
  • alkali phosphates which in Form of their alkaline neutral or acidic sodium or potassium salts can.
  • examples include trisodium phosphate, tetrasodium diphosphate, disodium dihydrogeridiphosphate, Pentasodium triphosphate, so-called sodium hexametaphosphate, oligomeric trisodium phosphate with degrees of oligomerization from 5 to 1000, especially 5 to 50, as well as mixtures of sodium and potassium salts. Your quantities can range up to about 55% by weight based on the total agent.
  • water-soluble builder components are organic, for example Polymers of native or synthetic origin, especially polycarboxylates act as a co-builder especially in hard water regions. Be considered for example polyacrylic acids and copolymers of maleic anhydride and acrylic acid as well as the sodium salts of these polymer acids. Commercial products are for Example Sökalan® CP 5, CP 10 and PA 30 from BASF.
  • Useful polymers of native origin include, for example, oxidized starches, such as known for example from international patent application WO 94/05762, and polyamino acids such as polyglutamic acid or polyaspartic acid.
  • hydroxycarboxylic acids such as Mono-, dihydroxysuccinic acid, ⁇ -hydroxypropionic acid and gluconic acid.
  • To the preferred Builder components include the salts of citric acid, in particular Sodium citrate.
  • Anhydrous trisodium citrate and preferably come as sodium citrate Trisodium citrate dihydrate.
  • Trisodium citrate dihydrate can be fine or coarse-crystalline powder can be used.
  • the pH value set can also be at least partially proportional to the corresponding co-builder salts mentioned acids are present.
  • the use of sodium percarbonate has particular advantages in cleaning agents for dishes, since it has a particularly favorable effect on the corrosion behavior on glasses.
  • the Oxygen-based bleach is therefore preferably an alkali percarbonate, especially sodium percarbonate.
  • too known peroxycarboxylic acids for example dodecanediperic acid or phthalimidopercarboxylic acids, which may optionally be substituted on the aromatic, are included.
  • the addition of small amounts of known bleach stabilizers such as for example of phosphonates, borates or metaborates and metasilicates and magnesium salts such as magnesium sulfate may be useful.
  • bleach activating acetonitrile derivatives essential to the invention according to formula I known conventional bleach activators, that is Compounds containing aliphatic peroxocarboxylic acids under perhydrolysis conditions preferably 1 to 10 carbon atoms, in particular 2 to 4 carbon atoms, and / or optionally substituted perbenzoic acid result can be used.
  • acylates are preferred Alkylenediamines, especially tetraacetylethylenediamine (TAED), acylated Triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, especially tetraacetylglycoluril (TAGU), N-acylimides, especially N-nonanoylsuccinimide (NOSI), carboxylic anhydrides, in particular Phthalic anhydride, acylated polyhydric alcohols, especially triacetin, ethylene glycol diacetate, 2,5-diacetoxy-2,5-dihydrofuran and those from the German Patent applications DE 196 16 693 and DE 196 16 767 known enol esters as well acetylated sorbitol and mannitol or their in the European Patent application EP 0 525 239 mixtures described (
  • German patent application DE 196 16 769 known hydrophilically substituted acylacetals and in German patent application DE 196 16 770 and international Patent application WO 95/14075 described acyllactams are also preferred used. Also known from German patent application DE 44 43 177 Combinations of conventional bleach activators can be used. such conventional bleach activators are in the usual range, preferably in Quantities from 0.1% by weight to 10% by weight, in particular 0.5% by weight to 7% by weight, based on total mean.
  • the sulfonimines and / or bleach-enhancing transition metal salts or transition metal complexes known from European patents EP 0 446 982 and EP 0 453 003 may also be present as so-called bleaching catalyst.
  • the transition metal compounds in question include, in particular, the manganese, iron, cobalt, ruthenium or molybdenum salen complexes known from German patent application DE 195 29 905 and their N-analog compounds known from German patent application DE 196 20 267, which consist of German patent application DE 195 36 082 known manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes, the manganese, iron, cobalt, ruthenium, molybdenum, titanium, described in German patent application DE 19605688 Vanadium and copper complexes with nitrogenous tripod ligands, the cobalt, iron, copper and ruthenium amine complexes known from German patent application DE 196 20 411, the manganese, copper described in German patent application DE 44 16 438 and cobalt complexes, the cobalt complexes described in European patent application EP 0 272 030, the manganese complexes known from European patent application EP 0 693 550 ,
  • bleach activators and transition metal bleach catalysts are known, for example, from German patent application DE-196 13 103 and international patent application WO 95/27775.
  • Bleach-enhancing transition metal salts and / or complexes, in particular with the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Hin, are used in customary amounts, preferably up to 1% by weight, in particular from 0.0025% by weight. % to 0.5% by weight and particularly preferably from 0.01% by weight to 0.1% by weight, in each case based on the total agent.
  • the particularly preferred bleach catalyst complexes include cobalt, iron, copper and ruthenium-amine complexes, for example [Co (NH 3 ) 5 Cl] Cl 2 and / or [Co (NH 3 ) 5 NO 2 ] Cl 2 .
  • the agents contain, in addition to the bleach activator according to formula I, which is made up in particulate form, a bleach-intensifying active ingredient combination which, according to European patent application EP 0 832 969, consists of intimately mixing a water-soluble salt of a divalent transition metal, selected from cobalt, iron, copper and ruthenium, and also their mixtures, a water-soluble ammonium salt and optionally an oxidizing agent based on peroxygen and inert carrier material are available in amounts of preferably 0.25% by weight to 25% by weight, in particular 1% by weight to 10% by weight; A preferred use of the bleach activator of the formula I, which is made up in particulate form, takes place in the presence of such a combination of active substances.
  • the machine dishwashing detergents according to the invention preferably contain the customary alkali carriers such as, for example, alkali silicates, alkali carbonates and / or alkali hydrogen carbonates.
  • Alkali silicates can be used in amounts of up to 40% by weight, based on the total agent. However, the use of the highly alkaline metasilicates as alkali carriers is preferably avoided entirely.
  • the alkali carrier system preferably used in the agents according to the invention is a mixture of carbonate and hydrogen carbonate, preferably sodium carbonate and hydrogen carbonate, which is contained in an amount of up to 50% by weight, preferably 5% by weight to 40% by weight , Depending on which pH is ultimately desired, the ratio of carbonate and bicarbonate used can be varied.
  • agents according to the invention are 20% by weight to 60% by weight of water-soluble organic builder, in particular alkali citrate, 3% by weight to Contain 20 wt .-% alkali carbonate and 5 wt .-% to 40 wt .-% alkali disilicate.
  • anionic, nonionic and / or amphoteric surfactants in particular weakly foaming nonionic surfactants, can also be added to the agents according to the invention, which serve to better detach fatty soils, as wetting agents and, if appropriate, as granulating aids in the preparation of the cleaning agents.
  • Their amount can be up to 20% by weight, in particular up to 10% by weight, and is preferably in the range from 0.5% by weight to 5% by weight.
  • Extremely low-foaming compounds are usually used in particular in cleaning agents for use in automatic dishwashing processes.
  • C 12 -C 18 alkyl polyethylene glycol polypropylene glycol ethers each containing up to 8 moles of ethylene oxide and propylene oxide units in the molecule.
  • you can also use other known low-foaming nonionic surfactants such as C 12 -C 18 alkyl polyethylene glycol polybutylene glycol ether, each with up to 8 moles of ethylene oxide and butylene oxide units in the molecule, end-capped alkyl polyalkylene glycol mixed ethers and the foaming but ecologically attractive C 8 -C 14- alkyl polyglucosides with a degree of polymerization of about 1 to 4 (e.g.
  • surfactants from the family of glucamides such as, for example, alkyl-N-methyl-glucamides, in which the alkyl part preferably originates from a fatty alcohol with the C chain length C 6 -C 14 . It is partially beneficial. if the surfactants described are used as mixtures, for example the combination of alkyl polyglycoside with fatty alcohol ethoxylates or glucamide with alkyl polyglycosides.
  • cleaning agents according to the invention can be used for cleaning silver corrosion inhibitors are used in dishes.
  • Preferred silver corrosion inhibitor are organic sulfides such as cystine and cysteine, divalent or trivalent Phenols.
  • optionally alkyl, aminoalkyl or aryl substituted triazoles such as Becizotriazole, isocyanuric acid, manganese, cobalt, titanium, zirconium, hafnium, vanadium or cerium salts and / or complexes in which the metals mentioned depend on the metal are in one of the oxidation states II, III, IV, V or VI.
  • the content of silver corrosion inhibitors in agents according to the invention is preferably in the range of 0.01% by weight to 1.5% by weight, in particular from 0.1% by weight to 0.5% by weight.
  • the manganese (III) - or known from international patent application WO 94/19445 Manganese (IV) complexes which in international patent application WO 94/07981 as Silver protection agent disclosed cysteine, which in the German patent application DE 195 18 693 as having a silver corrosion inhibiting effect alone or in particular in Combination with isocyanuric acid described cystine, and / or that in the German patent applications Titanium, described in DE 43 25 922 and DE 43 15 397, Zirconium, hafnium, vanadium, cobalt or cerium salts and / or complexes in which the metals are in one of the oxidation states II, III, IV, V or VI, and mentioned there Manganese (II) salts or complexes for preventing silver corrosion in the invention Funds are used.
  • the agents according to the invention can contain enzymes such as proteases, amylases, Contain pullulanases, cutinases and lipases, for example proteases such as BLAP®, Optimase®, Opticlean®, Maxacal®, Maxapem®, Esperase®, Savinase®, Purafect® OxP and / or Durazym®, amylases such as Termamyl®, Amylase-LT®, Maxamyl®, Duramyl® and / or Purafect® OxAm, lipases such as Lipolase®, Lipomax®, Lumafast® and / or Lipozym®.
  • proteases such as BLAP®, Optimase®, Opticlean®, Maxacal®, Maxapem®, Esperase®, Savinase®, Purafect® OxP and / or Durazym®
  • amylases such as Termamyl®, Amylase-LT®, Max
  • the optionally used enzymes can, as for example in the international patent applications WO 92/11347 or WO 94/23005
  • Carriers can be adsorbed and / or embedded in coating substances to protect them against premature Protect inactivation. They are in the cleaning agents according to the invention preferably in amounts up to 2% by weight, in particular from 0.1% by weight to 1.5% by weight. contain, particularly preferably enzymes stabilized against oxidative degradation, such as from international patent applications WO 94/02597, WO 94/02618, WO 94/18314, WO 94/23053 or WO 95/07350, known, are used become.
  • the cleaning agents foam too much during use, they can still preferably up to 6% by weight, in particular about 0.5% by weight to 4% by weight of one foam-suppressing compound, preferably from the group of silicone oils, mixtures made of silicone oil and hydrophobicized silica, paraffins, paraffin-alcohol combinations, hydrophobicized silica, the bis fatty acid amides, and others other known commercially available defoamers can be added.
  • one foam-suppressing compound preferably from the group of silicone oils, mixtures made of silicone oil and hydrophobicized silica, paraffins, paraffin-alcohol combinations, hydrophobicized silica, the bis fatty acid amides, and others other known commercially available defoamers can be added.
  • foam-suppressing compound preferably from the group of silicone oils, mixtures made of silicone oil and hydrophobicized silica, paraffins, paraffin-alcohol combinations, hydrophobicized silica, the bis fatty acid amides, and
  • the agents according to the invention cannot system and result from a self-determined pH value environmentally compatible acids, especially citric acid, acetic acid, tartaric acid, malic acid, Lactic acid, glycolic acid, succinic acid, glutaric acid and / or adipic acid, however also mineral acids, especially sulfuric acid or alkali hydrogen sulfates, or bases, in particular ammonium or alkali metal hydroxides.
  • environmentally compatible acids especially citric acid, acetic acid, tartaric acid, malic acid, Lactic acid, glycolic acid, succinic acid, glutaric acid and / or adipic acid
  • mineral acids especially sulfuric acid or alkali hydrogen sulfates, or bases, in particular ammonium or alkali metal hydroxides.
  • pH regulators are preferably not more than 10% by weight, in particular, in the agents according to the invention from 0.5% by weight to 6% by weight.
  • disintegration aids so-called tablet disintegrants
  • disintegration accelerators are understood as auxiliary substances which are necessary for the rapid disintegration of Tablets in water or gastric juice and ensure the release of the pharmaceuticals in an absorbable form.
  • the premixes to be compressed into tablets contain 0.5 to 10% by weight, preferably 1 to 5% by weight and in particular 2 to 4% by weight, of a disintegration aid, in each case based on the premix.
  • Disintegrants based on cellulose are used as preferred disintegrants in the context of the present invention, so that preferred detergent tablets contain such a disintegrant based on cellulose in amounts of 0.5 to 10% by weight, preferably 1 to 5% by weight and in particular 2 to 4% by weight .-% contain.
  • Pure cellulose has the formal gross composition (C 6 H 10 O 5 ) n and, formally speaking, is a ⁇ -1,4-polyacetal of cellobiose, which in turn is made up of two molecules of glucose.
  • Suitable celluloses consist of approx. 500 to 5000 Glucose units and consequently have average molecular weights of 50,000 to 500,000.
  • Cellulose-based disintegrants which can be used in the context of the present invention are also cellulose derivatives which can be obtained from cellulose by polymer-analogous reactions. Such chemically modified celluloses include, for example, products from esterifications or etherifications in which hydroxy hydrogen atoms have been substituted. However, celluloses in which the hydroxyl groups have been replaced by functional groups which are not bound via an oxygen atom can also be used as cellulose derivatives.
  • the group of cellulose derivatives includes, for example, alkali celluloses, carboxymethyl cellulose (CMC), cellulose esters and ethers and aminocelluloses.
  • the cellulose derivatives mentioned are preferably not used alone as disintegrants, but are used in a mixture with cellulose.
  • the content of cellulose derivatives in these mixtures is preferably below 50% by weight, particularly preferably below 20% by weight, based on the cellulose-based disintegrant. Pure cellulose which is free of cellulose derivatives is particularly preferably used as the cellulose-based disintegrant.
  • Microcrystalline cellulose can be used as a further cellulose-based disintegrant or as a component of this component.
  • microcrystalline cellulose is obtained by partial hydrolysis of celluloses under conditions which only attack and completely dissolve the amorphous areas (approx. 30% of the total cellulose mass) of the celluloses, but leave the crystalline areas (approx. 70%) undamaged.
  • a subsequent disaggregation of the microfine celluloses produced by the hydrolysis provides the microcrystalline celluloses, which have primary particle sizes of approximately 5 ⁇ m and can be compacted, for example, into granules with an average particle size of 200 ⁇ m.
  • the agents according to the invention are preferably powdered, granular or tablet-shaped preparations in a known manner, for example by Mixing, granulating, roller compacting and / or by spray drying the thermally resilient components and admixing the more sensitive components, which include in particular enzymes, bleaching agents and the bleach activator, can be produced.
  • agents according to the invention in the form of non-dusting, storage-stable free-flowing powders and / or granules with high bulk densities in the range of 800 up to 1000 g / l can be achieved in that the Builder components with at least a portion of liquid mixture components mixed by increasing the bulk density of this premix and subsequently - if desired after intermediate drying - the other components of the agent, including the particulate made up bleaching catalyst according to formula I with which premix thus obtained combined.
  • agents according to the invention are in the form compressed body, in particular tablets, before, for the manufacture of which Premix containing all the ingredients suitable above for agents according to the invention can, pressed.
  • the premix can be obtained from the be composed of different substances. Independent of Composition of the premixes to be compressed can have physical parameters the premixes are chosen so that advantageous molded body properties result.
  • the particulate to be pressed has Premixed bulk weights above 600 g / l, preferably above 700 g / l and especially above 800 g / l.
  • the compressed particulate premix has a particle size distribution in which less than 10% by weight, preferably less than 7.5% by weight, and in particular less than 5% by weight of the particles are larger than 1600 ⁇ m or smaller than 200 ⁇ m.
  • the particulate premix to be compressed has a particle size distribution in which more than 30% by weight, preferably more a particle size than 40% by weight and in particular more than 50% by weight of the particles show between 600 and 1000 ⁇ m.
  • the premix is made in a so-called The die is compacted between two punches to form a solid compact.
  • This process which is briefly referred to below as tableting, is divided into four Sections dosing, compression (elastic deformation), plastic deformation and Ejection.
  • the premix is first introduced into the die, the filling quantity and so that the weight and shape of the resulting molded body by the position of the lower stamp and the shape of the press tool can be determined.
  • the constant one Dosage even at high molding throughputs is preferably over a volumetric dosage of the premix reached.
  • the upper plunger touches the premix when tabletting and descends further of the lower stamp. With this compression, the particles of the premix pressed closer together, with the void volume within the filling between the stamps decreases continuously. From a certain position of the upper stamp (and thus from a certain pressure on the premix) the plastic begins Deformation in which the particles flow together and it to form the Shaped body comes.
  • premixed particles are crushed and it comes at even higher pressures to sinter the premix.
  • phase of elastic deformation is shortened more and more, so that the resulting shaped bodies can have more or less large cavities.
  • the finished molded body is made using the lower stamp pressed out of the die and by subsequent transport devices carried away. At this point, only the weight of the molded body is final determined because the compacts due to physical processes (stretching, crystallographic effects, cooling etc.) can still change their shape and size.
  • Tableting takes place in commercially available tablet presses, which are basically single or Double stamps can be equipped. In the latter case, not only the Upper stamp used to build up pressure, the lower stamp also moves during of the pressing process towards the upper punch, while the upper punch presses down.
  • Eccentric tablet presses are preferably used for small production quantities, where the stamp or stamps are attached to an eccentric disc, which in turn an axis with a certain rotational speed is mounted. The movement this ram is comparable to the way a conventional four-stroke engine works.
  • the pressing can be done with an upper and lower stamp, but it can also several stamps can be attached to an eccentric disc, the number of Die holes are expanded accordingly.
  • the throughputs of eccentric presses vary from a few hundred to a maximum of 3000 tablets per hour depending on the type.
  • rotary tablet presses are usually selected, on which a so-called matrix table a larger number of matrices circular is arranged.
  • the number of matrices varies between 6 and 55, depending on the model Larger matrices are also commercially available.
  • Every die is on the die table an upper and lower stamp assigned, again the pressure is active only by the upper or lower stamp, but can also be built up by both stamps.
  • the Matrix table and the stamp move around a common vertical Axis, the stamp with the help of rail-like cam tracks during circulation in the positions for filling, compression, plastic deformation and discharge to be brought.
  • Rotary tablet presses can also be equipped with single or multiple tools, so that, for example, an outer circle with 50 and an inner circle with 35 holes can be used for pressing at the same time.
  • the throughputs are more modern Rotary tablet presses are over a million tablets per hour.
  • Suitable tableting machines are available, for example, from the Apparatebau company Holzwarth GbR, Asperg, Wilhelm Fette GmbH, Schwarzenbek, Hofer GmbH, Weil, KILIAN, Cologne, KOMAGE, Kell am See, KORSCH Pressen GmbH, Berlin, Mapag Maschinenbau AG, Bern (CH) and Courtoy N.V., Halle (BE / LU).
  • Particularly suitable is for example the hydraulic double pressure press HPF 630 from LAEIS, D.
  • the moldings can be in a predetermined spatial shape and a predetermined size are manufactured. Practically all sensibly manageable come as a room shape Configurations into consideration, for example, the training as a board, the staff or Bar shape, cubes, cuboids and corresponding room elements with flat side surfaces as well as in particular cylindrical configurations with circular or oval Cross-section. This last embodiment covers the form of presentation from the tablet up to compact cylinder pieces with a ratio of height to diameter above 1.
  • the spatial shape of another embodiment of the shaped body is in its dimensions adapted the dosing chamber of commercial dishwashers, so that the Shaped bodies can be metered directly into the induction chamber without a metering aid where they are released from during the cleaning process. It goes without saying but also an easy use of the detergent tablets via dosing aids possible.
  • ⁇ stands for diametral fracture stress (DFS) in Pa
  • P is the force in N which leads to the pressure exerted on the molded body, which is the Breakage of the molded body causes
  • D is the molded body diameter in meters
  • t is the height of the moldings.
  • a particulate premix is pressed into a shaped body. Rather, extend the process to the extent that one in a conventional manner produces multilayered molded articles by making two or more premixes prepares that are pressed together. This is the premix that is filled in first slightly pre-pressed to create a smooth and parallel to the bottom of the molding To get top, and after filling the second premix to the finished Molded body finally pressed. In the case of three-layer or multi-layer moldings, each is carried out Pre-mix addition another pre-compression before adding the last Premixed the molded body is finally pressed.
  • Agents for cleaning dishes according to the invention can be used both in household dishwashers as used in commercial dishwashers. The addition is done by hand or by means of suitable dosing devices.
  • the application concentrations in the cleaning liquor are usually about 1 to 8 g / l, preferably 2 to 5 g / l.
  • a machine wash program is generally followed by some on the Cleaning cycle following intermediate rinse cycles with clear water and one. Rinse aid supplemented with a common rinse aid and ended. After this Drying is completely clean and in when using agents according to the invention hygienically perfect dishes.
  • Two-phase tablets M1 were produced by pressing the ingredients listed in the table below Composition of the 2-phase tablet (% by weight, based on the entire tablet) first phase second phase sodium tripolyphosphate 30 25 Na perborate monohydrate 10 - MMA Granulatat 3 - Polycarboxylate (Sokalan® CP5) 1 - nonionic surfactant 2 - sodium 15 - Sheet-silicate (SKS-6) 6 - Complexing agent (Turpinal® 2NZ) Protease Granules (Blap 200) - 2 Amylase granules (Duramyl® 60 T) - 2 dye - 0.9 Perfume - 0.1
  • tablets of the same composition were otherwise produced, which instead of the MMA granules were a mixture of 2% by weight of TAED ( V1 ) or 2% by weight of N-methylmorpholinium acetonitrile methosulfate ( V2 ) or 2% by weight of N-methylmorpholinium acetonitrile -Hydrogen sulfate (V3) each containing 1 wt .-% silica.
  • Table 2 shows the cleaning grades for the freshly prepared agents (initial value) and agents stored for 2 weeks (room temperature or 30 ° C, 80% relative humidity). cleaning notes output value Storage at room temperature Storage at 30 ° C, 80% rel.

Landscapes

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

Claims (21)

  1. Utilisation de composés, fabriqués sous forme particulaire à l'aide de matériaux de support inorganiques contenant du silicium, de formule générale I R1R2R3N+CH2CN X- dans laquelle R1, R2 et R3 représentent indépendamment un groupe alkyle, alcényle ou aryle comprenant de 1 à 18 atomes de C, les groupes R2 et R3 pouvant également constituer une partie d'un hétérocycle contenant un atome de N et éventuellement d'autres hétéroatomes, et X est un anion équilibreur de charge, en tant qu'activateurs notamment pour des composés peroxydes inorganiques, dans des détergents solides pour la vaisselle qui sont mis en oeuvre dans des solutions de lavage essentiellement aqueuses, pour le blanchiment de salissures provenant du thé.
  2. Utilisation selon la revendication 1, caractérisée en ce que le matériau de support inorganique contenant du silicium présente une surface intérieure de l'ordre de 10 m2/g à 500 m2/g, en particulier de 100 m2/g à 450 m2/g.
  3. Utilisation selon la revendication 1 ou 2, caractérisée en ce que le matériau de support inorganique contenant du silicium est choisi dans le groupe comprenant des silicates, des acides siliciques, des gels de silice et des argiles, ainsi que leurs mélanges.
  4. Utilisation selon l'une quelconque des revendications 1 à 3, caractérisée en ce que la forme particulaire comprend de 10 à 50 % en poids du matériau de support contenant du silicium et de 50 à 90 % en poids du composé de formule I.
  5. Utilisation selon l'une quelconque des revendications 1 à 4, caractérisée en ce que dans le composé de formule I, R2 et R3 forment, avec l'atome de N quaternaire, un cycle morpholinium.
  6. Utilisation selon la revendication 5, caractérisée en ce que dans le composé de formule I, R1 représente un groupe alkyle comprenant de 1 à 3 atomes de C, en particulier un groupe méthyle.
  7. Utilisation selon l'une quelconque des revendications 1 à 6, caractérisée en ce que l'anion équilibreur X- est choisi parmi les halogénures, tels que les chlorures, fluorures, iodures et bromures, les nitrates, les hydroxydes, les hexafluorophosphates, les sulfates, les hydrogénosulfates, les métho- et éthosulfates, les chlorates, les perchlorates et les anions d'acides carboxyliques, tels que les formiates, acétates, benzoates ou citrates.
  8. Utilisation selon l'une quelconque des revendications 1 à 7, caractérisée en ce que l'anion équilibreur X- est un sulfate, un hydrogénosulfate ou un méthosulfate.
  9. Utilisation selon l'une quelconque des revendications 1 à 8, caractérisée en ce que le composé peroxyde qui doit être activé est choisi dans le groupe comprenant des peracides organiques, le peroxyde d'hydrogène, des perborates et percarbonates, ainsi que des mélanges de ces composés.
  10. Utilisation selon l'une quelconque des revendications 1 à 9, caractérisée en ce qu'est simultanément présente une combinaison d'agents actifs renforçant l'action de blanchiment, qui est obtenue par mélange intime d'un sel hydrosoluble d'un métal de transition divalent choisi parmi le cobalt, le fer, le cuivre et le ruthénium ainsi que des mélanges de ces métaux, d'un sel d'ammonium hydrosoluble et éventuellement d'un agent oxydant à base de peroxyde, ainsi que d'un matériau de support inerte.
  11. Produit destiné au lavage de la vaisselle, caractérisé en ce qu'il contient de 1 % en poids à 10 % en poids, en particulier de 2 % en poids à 6 % en poids, d'un composé fabriqué sous forme particulaire, à l'aide de matériaux de support inorganiques contenant du silicium, de formule générale I R1R2R3N+CH2CN X- dans laquelle R1, R2 et R3 représentent indépendamment un groupe alkyle, alcényle ou aryle comprenant de 1 à 18 atomes de C, les groupes R1 et R2 pouvant également constituer une partie d'un hétérocycle contenant un atome de N et éventuellement d'autres hétéroatomes, et X est un anion équilibreur de charge, en plus de composants usuels compatibles avec le composé de formule I.
  12. Produit destiné au lavage en machine de la vaisselle; contenant de 15 % en poids à 70 % en poids, en particulier de 20 % en poids à 60 % en poids de composants builders hydrosolubles, de 5 % en poids à 25 % en poids, en particulier de 8 % en poids à 17 % en poids d'agents de blanchiment à base d'oxygène, toujours par rapport au poids total du produit, caractérisé en ce qu'il contient un composé fabriqué sous forme particulaire, à l'aide de matériaux de support inorganiques contenant du silicium, de formule générale I, en particulier dans des proportions de 2 % en poids à 6 % en poids.
  13. Produit selon la revendication 11 ou 12, caractérisé en ce qu'il contient un composé à base de peroxyde choisi dans le groupe comprenant des peracides organiques, le peroxyde d'hydogène, des perborates et des percarbonates, ainsi que des mélanges de ces composés.
  14. Produit selon l'une quelconque des revendications 11 à 13, caractérisé en ce qu'en plus des composés de formule I, des composés libérant des acides peroxocarboxyliques dans des conditions de perhydrolyse sont présents dans des proportions de 0,5 % en poids à 7 % en poids.
  15. Produit selon l'une quelconque des revendications 11 à 14, caractérisé en ce qu'il contient, en plus des composés de formule I, une combinaison d'agents actifs renforçant l'action de blanchiment, qui est obtenue par mélange intime d'un sel hydrosoluble d'un métal de transition divalent, choisi parmi le cobalt, le fer, le cuivre et le ruthénium, ainsi que des mélanges de ces métaux, d'un sel d'ammonium hydrosoluble et éventuellement d'un agent oxydant à base de peroxyde, ainsi que d'un matériau de support inerte.
  16. Produit selon l'une quelconque des revendications 11 à 14, caractérisé en ce qu'en plus du composé de formule I, des sels ou complexes de métaux de transition catalyseurs de blanchiment sont présents, en particulier dans des proportions de 0,0025 % en poids à 0,5 % en poids.
  17. Produit selon la revendication 16, caractérisé en ce qu'en plus du composé de formule I, des complexes d'amines du cobalt, du fer, du cuivre ou du ruthénium, catalyseurs de blanchiment, en particulier [Co(NH3)5Cl]Cl2 et/ou [Co(NH3)5 NO2]Cl2 sont présents.
  18. Produit selon l'une quelconque des revendications 11 à 17, caractérisé en ce qu'il se présente sous forme de pastilles.
  19. Produit selon la revendication 18, caractérisé en ce que les pastilles se présentent sous forme bicouche.
  20. Produit selon la revendication 19, caractérisé en ce que dans l'une des couches, il comprend l'agent de blanchiment sous la forme du composé peroxyde en particulier inorganique, et dans la deuxième couche, l'activateur de blanchiment fabriqué sous forme particulaire, de formule I.
  21. Produit selon la revendication 19, caractérisé en ce qu'il contient, dans la même couche, l'agent de blanchiment sous forme du composé peroxyde en particulier inorganique et l'activateur de blanchiment fabriqué sous forme particulaire de formule I, et dans une deuxième couche, les autres constituants sensibles, notamment les enzymes.
EP99962240A 1998-12-15 1999-12-08 Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides Expired - Lifetime EP1141211B1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE19857596 1998-12-15
DE19857596A DE19857596A1 (de) 1998-12-15 1998-12-15 Teilchenförmig konfektionierte Acetonitril-Derivate als Bleichaktivatoren in festen Reinigungsmitteln
US12691999P 1999-03-29 1999-03-29
US126919P 1999-03-29
PCT/EP1999/009622 WO2000036061A2 (fr) 1998-12-15 1999-12-08 Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides

Publications (2)

Publication Number Publication Date
EP1141211A2 EP1141211A2 (fr) 2001-10-10
EP1141211B1 true EP1141211B1 (fr) 2004-02-25

Family

ID=26050748

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99962240A Expired - Lifetime EP1141211B1 (fr) 1998-12-15 1999-12-08 Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides

Country Status (6)

Country Link
US (1) US6407045B1 (fr)
EP (1) EP1141211B1 (fr)
JP (1) JP2002532615A (fr)
KR (1) KR100630289B1 (fr)
ES (1) ES2216609T3 (fr)
WO (1) WO2000036061A2 (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19914811A1 (de) * 1999-03-31 2000-10-05 Henkel Kgaa Enzym- und bleichaktivatorhaltige Wasch- und Reinigungsmittel
DE19914812A1 (de) * 1999-03-31 2000-10-05 Henkel Kgaa Ein- oder mehrphasige Wasch- und Reinigungsmittelformkörper mit speziellen Bleichaktivatoren
DE19914353A1 (de) * 1999-03-31 2000-10-05 Henkel Kgaa Wasch- und Reinigungsmittelformkörper mit speziellen Bleichaktivatoren
DE10038845A1 (de) * 2000-08-04 2002-02-21 Henkel Kgaa Teilchenförmig konfektionierte Acetonitril-Derivate als Bleichaktivatoren in festen Waschmitteln
DE10038832A1 (de) * 2000-08-04 2002-03-28 Henkel Kgaa Umhüllte Bleichaktivatoren
DE10038180A1 (de) * 2000-08-04 2002-02-14 Reckitt Benckiser Nv Verwendung eines neuartigen Bleichaktivator-Compounds in Geschirrspülmittelzusammensetzungen
DE10057045A1 (de) 2000-11-17 2002-05-23 Clariant Gmbh Teilchenförmige Bleichaktivatoren auf der Basis von Acetonitrilen
DE10121051A1 (de) 2001-04-28 2002-10-31 Clariant Gmbh Builder-Zusammensetzung
DE10159388A1 (de) * 2001-12-04 2003-06-12 Henkel Kgaa Verfahren zur Herstellung von umhüllten Bleichaktivatorgranulaten
DE10161766A1 (de) * 2001-12-15 2003-06-26 Clariant Gmbh Bleichaktivator-Co-Granulate
DE10211389A1 (de) * 2002-03-15 2003-09-25 Clariant Gmbh Ammoniumnitrile und deren Verwendung als hydrophobe Bleichaktivatoren
US20070259801A1 (en) * 2006-03-31 2007-11-08 Szu-Min Lin Composition for a foam pretreatment for medical instruments
DE102006036889A1 (de) * 2006-08-04 2008-02-07 Clariant International Limited Verwendung von Aminoacetonen und deren Salzen als Bleichkraftverstärker für Persauerstoffverbindungen
GB0616439D0 (en) * 2006-08-18 2006-09-27 Reckitt Benckiser Nv Detergent composition
GB0917951D0 (en) * 2009-10-14 2009-11-25 Chemlink Specialities Ltd Composition including one or more hydrolytically unstable components
EP3033411B1 (fr) * 2013-08-14 2019-12-04 Budich International GmbH Tablette de nettoyage à plusieurs phases

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9011618D0 (en) * 1990-05-24 1990-07-11 Unilever Plc Bleaching composition
US5520835A (en) * 1994-08-31 1996-05-28 The Procter & Gamble Company Automatic dishwashing compositions comprising multiquaternary bleach activators
US5814242A (en) * 1995-06-07 1998-09-29 The Clorox Company Mixed peroxygen activator compositions
US5888419A (en) * 1995-06-07 1999-03-30 The Clorox Company Granular N-alkyl ammonium acetontrile compositions
DE19605526A1 (de) * 1996-02-15 1997-08-21 Hoechst Ag Ammoniumnitrile und deren Verwendung als Bleichaktivatoren
ES2233987T3 (es) * 1996-09-26 2005-06-16 Henkel Kommanditgesellschaft Auf Aktien Combinacion de productos activos cataliticamente para reforzar el efecto de blanqueo.
EP1036070B1 (fr) * 1996-11-29 2004-02-18 The Clorox Company Sels d'acetonitrile d'ammonium n-alkyle, procedes associes et compositions contenant ces sels
DE19649375A1 (de) * 1996-11-29 1998-06-04 Henkel Kgaa Acetonitril-Derivate als Bleichaktivatoren in Reinigungsmitteln
US5900395A (en) * 1996-12-23 1999-05-04 Lever Brothers Company Machine dishwashing tablets containing an oxygen bleach system
US5783540A (en) * 1996-12-23 1998-07-21 Lever Brothers Company, Division Of Conopco, Inc. Machine dishwashing tablets delivering a rinse aid benefit
DE19713852A1 (de) * 1997-04-04 1998-10-08 Henkel Kgaa Aktivatoren für Persauerstoffverbindungen in Wasch- und Reinigungsmitteln

Also Published As

Publication number Publication date
JP2002532615A (ja) 2002-10-02
US6407045B1 (en) 2002-06-18
KR100630289B1 (ko) 2006-09-29
ES2216609T3 (es) 2004-10-16
WO2000036061A3 (fr) 2000-09-14
WO2000036061A2 (fr) 2000-06-22
EP1141211A2 (fr) 2001-10-10
US20020032139A1 (en) 2002-03-14
KR20010080769A (ko) 2001-08-22

Similar Documents

Publication Publication Date Title
EP1141211B1 (fr) Derives d'acetonitrile confectionnes sous forme de particules utilises comme activateurs de blanchiment dans des detergents solides
US20040067863A1 (en) Enclosed bleach activators
EP1305384B1 (fr) Derives acetonitrile concus sous forme particulaire servant d'activateurs de blanchiment dans des lessives solides
DE19908051A1 (de) Verfahren zur Herstellung compoundierter Acetonitril-Derivate
DE19758176A1 (de) Geschirrspülmittelformkörper mit Tensiden
WO1999035235A1 (fr) Corps moules detergents pour lave-vaisselle renfermant des agents de blanchiment chlores
WO1999035233A1 (fr) Procede de fabrication d'un corps moule detergent pour lave-vaisselle
EP0832969B1 (fr) Composé catalytique actif pour améliorer l'efficacité de blanchiment
WO1999035230A1 (fr) Corps moules de solubilite specifique destinee au lavage de la vaisselle
DE19758181A1 (de) Geschirrspülmittelformkörper mit Soil-Release-Polymeren
DE19908069A1 (de) Compoundierte Acetonitril-Derivate als Bleichaktivatoren in Reinigungsmitteln
EP1044255A1 (fr) Agents pour laver la vaisselle sous forme de corps moules contenant des activateurs de blanchiment
DE19857596A1 (de) Teilchenförmig konfektionierte Acetonitril-Derivate als Bleichaktivatoren in festen Reinigungsmitteln
EP1045895A1 (fr) Corps moules detergents pour lave-vaisselle a geometrie specifique
WO1999035231A1 (fr) Corps moules actifs en termes de lavage et de surface specifique
EP1045894A1 (fr) Corps moule detergent pour lave-vaisselle a proportions volumiques specifiques
EP1969112B1 (fr) Détergent contenant des complexes ayant une activité catalytique de blanchiment
DE19959589A1 (de) Mehrphasige Reinigungsmitteltabletten

Legal Events

Date Code Title Description
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

17P Request for examination filed

Effective date: 20010606

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

RIN1 Information on inventor provided before grant (corrected)

Inventor name: HUESTIS, SUSAN, P.

Inventor name: LIETZMANN, ANDREAS

Inventor name: HAERER, JUERGEN

Inventor name: SPECKMANN, HORST-DIETER

Inventor name: NITSCH, CHRISTIAN

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE ES FR GB IT NL

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

XX Miscellaneous (additional remarks)

Free format text: DERZEIT SIND DIE WIPO-PUBLIKATIONSDATEN A3 NICHT VERFUEGBAR.

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: GERMAN

REF Corresponds to:

Ref document number: 59908672

Country of ref document: DE

Date of ref document: 20040401

Kind code of ref document: P

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)

Effective date: 20040625

REG Reference to a national code

Ref country code: IE

Ref legal event code: FD4D

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2216609

Country of ref document: ES

Kind code of ref document: T3

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20041126

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

Ref country code: NL

Payment date: 20071203

Year of fee payment: 9

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

Ref country code: IT

Payment date: 20071221

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: 20071205

Year of fee payment: 9

Ref country code: FR

Payment date: 20071210

Year of fee payment: 9

Ref country code: ES

Payment date: 20080118

Year of fee payment: 9

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

Ref country code: DE

Payment date: 20071206

Year of fee payment: 9

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20081208

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20090701

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20090831

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

Ref country code: DE

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

Effective date: 20090701

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

Ref country code: NL

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

Effective date: 20090701

Ref country code: GB

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

Effective date: 20081208

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20081209

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

Ref country code: FR

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

Effective date: 20081231

Ref country code: ES

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

Effective date: 20081209

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

Ref country code: IT

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

Effective date: 20081208