WO2006045450A1 - Unite de dosage d'agent de lavage ou de nettoyage - Google Patents

Unite de dosage d'agent de lavage ou de nettoyage Download PDF

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Publication number
WO2006045450A1
WO2006045450A1 PCT/EP2005/011064 EP2005011064W WO2006045450A1 WO 2006045450 A1 WO2006045450 A1 WO 2006045450A1 EP 2005011064 W EP2005011064 W EP 2005011064W WO 2006045450 A1 WO2006045450 A1 WO 2006045450A1
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WO
WIPO (PCT)
Prior art keywords
combination product
acid
product according
cleaning agent
booster
Prior art date
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PCT/EP2005/011064
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German (de)
English (en)
Inventor
Pavel Gentschev
Arnd Kessler
Ulrich Pegelow
Christian Nitsch
Arno DÜFFELS
Original Assignee
Henkel Kommanditgesellschaft Auf Aktien
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.)
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Priority claimed from DE102004051560A external-priority patent/DE102004051560A1/de
Application filed by Henkel Kommanditgesellschaft Auf Aktien filed Critical Henkel Kommanditgesellschaft Auf Aktien
Publication of WO2006045450A1 publication Critical patent/WO2006045450A1/fr

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    • 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
    • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • 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
    • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means

Definitions

  • the present invention is in the field of detergents or cleaners, especially combination products for automatic dishwashing.
  • Machine dishwashing detergents are available to the consumer in a variety of forms.
  • this offer also includes, for example, detergent concentrates in the form of extruded or tabletted compositions.
  • These fixed, concentrated or compressed forms of supply are characterized by a reduced volume per dosing unit and thus reduce the costs for packaging and transport.
  • the washing or cleaning agent tablets additionally meet the consumer's desire for simple dosing.
  • the corresponding means are comprehensively described in the prior art.
  • compacted detergents also have a number of disadvantages.
  • Especially tableted supply forms are characterized by their high compression often by a delayed disintegration and thus a delayed release of their ingredients.
  • WO 01/83657 A2 Procter & Gamble
  • pouches which contain two particulate solids in a receiving chamber, each of which is present in fixed regions and does not mix with one another.
  • EP 1 256 623 A1 Subject of the European application EP 1 256 623 A1 (Procter & Gamble) is a kit of at least two bags with different composition and optics. The bags are separate and not as a compact single product.
  • the present application was therefore based on the object of providing a machine dishwashing detergent which has an improved cleaning and final-rinse profile on the basis of previously known forms of supply and raw materials, preferably while at the same time reducing water and energy consumption during the automatic dishwashing process.
  • a first subject of the present application is therefore a combined automatic dishwashing product comprising a) a compartment containing a detergency booster; b) another compartment containing a main cleaning agent; and (c) an instruction manual instructing the user to use the scrubber in the pre-rinse cycle and to use the main detergent in the main rinse of a machine dishwashing process.
  • the detergency booster and main cleaning agents included in the compositions of the invention act in successive rinses of a machine dishwashing cycle, supplement and / or enhance one another with regard to their effect and bring about improved cleaning and rinsing performance.
  • the instructions for use allow the representation and communication of the exact mode of use of detergency booster and main cleaning agent to achieve the beneficial effect of the composition according to the invention. This presentation or communication can be done, for example, in visual and / or written and / or acoustic means.
  • the washing power booster and the main cleaning agent are two automatic dishwashing detergents of different composition.
  • the washing power booster and the main cleaning agent are two automatic dishwashing detergents of different composition.
  • the detergency booster and the main cleaning agent have at least one common packaging system.
  • the detergency booster and the main cleaning agent are offered in a common primary and / or secondary packaging.
  • the primary packaging while the package is called, which is directly on the inside with the washing power booster and / or the main cleaning agent in contact.
  • a common primary packaging for washing power booster and main cleaning agents are, for example, bags or bags.
  • the group of these sacks and bags also includes, for example, those packaging systems which are known in the art as the "flow pack.”
  • the secondary packaging serves to further package and package the means in the primary packaging and is not in direct contact with these means Contact
  • the secondary packaging usually corresponds to the outer packaging of the sales product. Examples of such secondary packaging are cardboard or foil bags, for example in the form of a stand-up pouch.
  • the preferably used as packaging system bags or bags of single-layer or laminated paper or plastic film can be designed in a variety of ways, such as inflated bag without center seam or bags with center seam, which closed by heat (heat fusion), adhesives or adhesive tapes become.
  • Single-layer bag or bag materials are the known papers, which may optionally be impregnated, as well as plastic films, which may optionally be coextruded.
  • Plastic films which can be used as packaging systems in the context of the present invention are given, for example, in Hans Domininghaus "Die Kunststoffe und Hästoff", 3rd edition, VDI Verlag, Dusseldorf, 1988, page 193.
  • particularly preferred combinations contain as packaging system a bag or bag of single-layer or laminated plastic film having a thickness of 10 to 200 .mu.m, preferably from 20 to 100 .mu.m and in particular from 25 to 50 microns.
  • Packaging systems are referred to as "different" packaging systems, which differ in terms of their chemical or physical properties (composition, thickness, etc.)
  • An example of this is a washing power intensifier and a main cleaning agent, which are packaged in different bags or sacks.
  • the detergency booster and the main cleaning agent are surrounded by a common primary packaging
  • the amount of the automatic dishwashing agent present in the primary packaging preferably corresponds to the dosing unit for one application, that is to say for a machine wash cycle
  • several of these primary-packaged metering units for a machine wash cycle are packaged together in an additional secondary packaging.
  • this first secondary packaging is surrounded by a second secondary packaging.
  • the washing power booster and the main cleaning agent have different primary packaging, but a common secondary packaging.
  • This common secondary packaging may optionally be surrounded by a second secondary packaging.
  • packaging systems in which the washing power booster and the main cleaning agent have neither a common primary nor a common secondary packaging.
  • Combination product characterized in that the detergency booster and the main cleaning agent have no common packaging system, according to the invention are preferred.
  • the primary packaging 1 and 2 and the secondary packaging 1 and 2 may be made of the same or different material.
  • At least one of the packages used preferably has a moisture vapor transmission rate of 0.1 g / m 2 / day to less than 20 g / m 2 / day when the packaging system is at 23 ° C and a relative equilibrium moisture content of 85 % is stored.
  • the temperature and humidity conditions mentioned are the test conditions specified in DIN standard 53122, with minimum deviations permissible according to DIN 53122 (23 ⁇ 1 ° C, 85 ⁇ 2% relative humidity).
  • the moisture vapor transmission rate of a given packaging system or material can be determined by other standard methods and is also, for example, in the ASTM standard E-96-53T (test for measuring water vapor transmission of material in sheet form) and TAPPI standard T464 m-45 ("Water Vapor Permeability of Sheet Materials at High Temperature Humidity").
  • the measuring principle of common methods is based on the water absorption of anhydrous calcium chloride, which is stored in a container in the appropriate atmosphere, the container is sealed at the top with the material to be tested. From the surface of the container, which is closed with the material to be tested (permeation surface), the increase in weight of the calcium chloride and the exposure time, the moisture vapor transmission rate decreases
  • A is the area of the material to be tested in cm 2
  • x is the weight gain of calcium chloride in g
  • y is the exposure time in h.
  • the relative equilibrium moisture in the measurement of the moisture vapor transmission rate in the context of the present invention is 85% at 23 ° C.
  • the absorption capacity of air for water vapor rises with the temperature up to a respective maximum content, the so-called saturation content, and is given in g / m 3.
  • the relative equilibrium moisture content of 85% at 23 ° C can be precisely adjusted to +/- 2% RH in laboratory chambers with humidity control, depending on the device type.
  • Even saturated solutions of certain salts form constant and well-defined relative humidities in closed systems at a given temperature, which are based on the phase equilibrium between the partial pressure of the water, the saturated solution and the body of the soil.
  • Packaging systems preferred in the present invention have a moisture vapor transmission rate of from 0.5 g / m 2 / day to less than 15 g / m 2 / day.
  • the packaging system of the combination according to the invention may consist of a wide variety of materials and take on any external forms. For economic reasons and for reasons of easier processability, however, packaging systems are preferred in which the packaging material has a low weight, is easy to process and inexpensive.
  • the packaging system consists of a bag or sack of single-layer or laminated paper and / or plastic film.
  • the means may be unsorted, i. as a loose filling, be filled in a bag of the materials mentioned.
  • the above-mentioned "flow packs" are suitable for individual application units of the detergent tablets, which are located in a bag or sack.
  • the detergency booster and the main cleaning agent of the combination according to the invention contain, depending on their intended use, ingredients of automatic dishwashing detergents in varying amounts.
  • Preferred detergency booster and main cleaning agent are characterized in that the detergency booster or the main cleaning agent has a relative equilibrium moisture content of less than 30% at 35 ° C / have.
  • the relative equilibrium moisture content of the detergency booster and main cleaning agent can be determined by conventional methods, wherein the following procedure was selected in the present studies: A water-impermeable 1-liter vessel with a lid, which has a closable opening for the introduction of samples, was with a total of 300 g of detergency booster or main cleaning agent filled and held for 24 h at a constant 23 C C to ensure a uniform temperature of the vessel and substance.
  • the water vapor pressure in the room via means can then be determined with a hygrometer (Hygrotest 6100, Testoterm Ltd., England). The water vapor pressure is now measured every 10 minutes until two consecutive values show no deviation (equilibrium moisture).
  • the above-mentioned hygrometer allows a direct display of the recorded values in% relative humidity.
  • both such agents as combination products within the scope of the present application, in which the detergency booster and the main cleaning agent are present together in a primary and / or secondary packaging, as well as those means in which the detergency booster and the main cleaning agent in each other separate primary or secondary packaging.
  • the detergency booster and main cleaning agent contained in the combination products according to the invention may be in solid or liquid form.
  • ready-to-use forms are liquid (s), in particular melts, and / or gel (s) and / or powder and / or granules (e) and / or extrudate (s) and / or compact (e) t.
  • liquid in the present application denotes substances or substance mixtures as well as solutions or suspensions which are in the liquid state of matter.
  • Combination products characterized in that the detergency booster and / or the main cleaning agent is present in the form of a liquid, are inventively preferred.
  • Powder is a general term for a form of division of solids and / or mixtures obtained by comminution, that is, grinding or crushing in the mortar (pulverization), grinding in mills or as a result of atomization or freeze-drying.
  • a particularly fine division is often called atomization or micronization; the corresponding powders are called micro-powders.
  • After the grain size is a rough division of the powder in coarse, fine u.
  • Very fine powder usual; A more detailed classification of powdery bulk solids is made by their bulk density and sieve analysis.
  • preferred powders have lower particle sizes below 5000 .mu.m, preferably less than 3000 .mu.m, preferably less than 1000 .mu.m, very particularly preferably between 50 and 1000 .mu.m and in particular between 100 and 800 .mu.m.
  • Powders can be compacted and agglomerated by extrusion, pressing, rolling, briquetting, pelleting and related processes.
  • Each of the methods known in the prior art for the agglomeration of particulate mixtures is in principle suitable for producing the solids contained in the agents according to the invention.
  • agglomerates used as solid (s) are, in addition to the granules, the compacts and extrudates.
  • Combination products characterized in that the detergency booster and / or the main cleaning agent is / are present in the form of a powder, are preferred according to the invention.
  • Granules are aggregates of granules.
  • a granule (granule) is an asymmetric aggregate of powder particles.
  • Granulation methods are widely described in the art.
  • Granules can be prepared by wet granulation, by dry granulation or compaction and by melt solidification granulation.
  • the most common granulation technique is wet granulation, since this technique is subject to the fewest restrictions and leads most safely to granules with favorable properties.
  • the wet granulation is carried out by moistening the powder mixtures with solvents and / or Amsterdamsmitteilemischen and / or solutions of binders and / or solutions of adhesives and is preferably carried out in mixers, fluidized beds or spray towers, said mixer can be equipped, for example, with stirring and kneading tools.
  • combinations of fluidized bed (s) and mixer (s) or combinations of different mixers can also be used for the granulation.
  • the granulation is dependent on the starting material and the desired product properties under the action of low to high shear forces.
  • melt solidification melting
  • aqueous, slurries spray drying
  • solid substances which are sprayed at the top of a tower in a defined droplet size, solidify in free fall or dry and on Floor of the tower incurred as granules.
  • Melt solidification is generally particularly suitable for shaping low-melting substances which are stable in the melting temperature range (eg urea, ammonium nitrate and various formulations such as enzyme concentrates, pharmaceuticals etc.), the corresponding granules are also referred to as prills.
  • Spray drying is used especially for the production of detergents or detergent ingredients.
  • extruder or perforated roll granulations in which optional powder mixtures mixed with granulating liquid are plastically deformed during perforation by perforated disks (extrusion) or on perforated rolls.
  • the products of extruder granulation are also referred to as extrudates.
  • Combination products characterized in that the detergency booster and / or the main cleaning agent is / are present in the form of a granulate, are preferred according to the invention.
  • the washing power booster or the main cleaning agent in particular the compacts and in particular the tablets are suitable.
  • Combination products characterized in that the detergency booster and / or the main cleaning agent in the form of a compact, preferably in the form of a tablet, are preferred according to the invention.
  • the detergency booster is in particulate form, preferably in the form of a powder or granules, while the main cleaning agent is in the form of a compact dosing unit, preferably in the form of a tablet or a filled water-soluble container ,
  • the washing power booster and the main cleaning agent are automatic dishwashing detergents of different composition.
  • all active ingredients known to the skilled person as ingredients of automatic dishwashing detergents are also suitable as ingredients of the detergency booster.
  • Combination products characterized in that the detergency booster contains a builder and / or a bleaching agent, preferably in amounts above 10 wt .-%, preferably above 20 wt .-% and in particular above 40 wt .-%, according to the invention are preferred.
  • the builders include in particular the phosphates, silicates and alkali carriers.
  • alkali metal phosphates with a particular preference for pentasodium or pentapotassium triphosphate (sodium or potassium tripolyphosphate), have the greatest importance in the washing and cleaning agent industry.
  • Alkali metal phosphates is the summary term for the alkali metal (especially sodium and potassium) salts of various phosphoric acids, in which one can distinguish metaphosphoric acids (HPO 3 ) n and orthophosphoric H 3 PO 4 in addition to higher molecular weight representatives.
  • the phosphates combine several advantages: they act as alkali carriers, prevent lime deposits on machine parts or lime incrustations in fabrics and also contribute to the cleaning performance.
  • Suitable phosphates are for example the sodium dihydrogen phosphate, NaH 2 PO 4 , in the form of the dihydrate (density 1, 91 like “3 , melting point 60 °) or in the form of the monohydrate (density 2.04 like “ 3 ), the disodium hydrogen phosphate (secondary sodium phosphate) , Na 2 HPO 4 , which is anhydrous or with 2 mol (density 2.066 like '3 , water loss at 95 °), 7 mol (density 1, 68 like "3 , melting point 48 ° with loss of 5 H 2 O) and 12 mol Water (density 1, 52 like '3 , melting point 35 ° with loss of 5 H 2 O) can be used, but especially the trisodium phosphate (tertiary sodium phosphate) Na 3 PO 4 , which as dodecahydrate, as decahydrate (corresponding to 19-20% P Z O 5 ) and in anhydrous form (corresponding to 39-40% P 2 O 5 ) can be
  • Another preferred phosphate is the tripotassium phosphate (tertiary or tribasic potassium phosphate), K 3 PO 4 .
  • the tetrasodium diphosphate sodium pyrophosphate
  • Na 4 P 2 O 7 which in anhydrous form (density 2.534 like “3 , melting point 988 °, also indicated 880 °) and as decahydrate (density 1, 815-1, 836 like " 3 , melting point 94 ° with loss of water)
  • potassium salt potassium diphosphate potassium 4 P 2 O 7 .
  • pentasodium triphosphate Na 5 P 3 O 10 (sodium tripolyphosphate)
  • the corresponding potassium salt Pentakaliumtriphosphat, K 5 P 3 Oi 0 potassium tripolyphosphate
  • the potassium polyphosphates are widely used in the washing and cleaning industry.
  • sodium potassium tripolyphosphates which are also within the scope of the present invention can be used. These arise, for example, when hydroxysing sodium trimetaphosphate with KOH:
  • phosphates are used as part of the detergency booster in the present application, these means contain the phosphate (s), preferably alkali metal phosphate (s), particularly preferably pentasodium or Pentakaliumtriphosphat (sodium or potassium tripolyphosphate), preferably in amounts of From 5 to 80% by weight, preferably from 15 to 75% by weight, in particular from 20 to 70% by weight, in each case based on the weight of the detergency booster.
  • alkali metal phosphate preferably pentasodium or Pentakaliumtriphosphat (sodium or potassium tripolyphosphate)
  • From 5 to 80% by weight preferably from 15 to 75% by weight, in particular from 20 to 70% by weight, in each case based on the weight of the detergency booster.
  • potassium tripolyphosphate and sodium tripolyphosphate in a weight ratio of more than 1: 1, preferably more than 2: 1, preferably more than 5: 1, more preferably more than 10: 1 and in particular more than 20: 1. It is particularly preferred to use exclusively potassium tripolyphosphate without admixtures of other phosphates.
  • Suitable crystalline, layered sodium silicates have the general formula NaMSi x O 2x + 1
  • x is a number from 1, 9 to 4 and y is a number from 0 to 20 and preferred values for x are 2, 3 or 4.
  • Preferred crystalline layered silicates of the formula given are those in which M is sodium and x assumes the values 2 or 3. In particular, both ⁇ - and ⁇ -sodium disilicates Na 2 Si 2 O 5 .yH 2 O are preferred.
  • crystalline layered silicates of general formula NaMSi x O 2x + 1 • y H 2 O are used, wherein M is sodium or hydrogen, x is a number from 1, 9 to 22, preferably from 1 , 9 to 4, and y is a number from 0 to 33.
  • y H 2 O are sold, for example, by the company Clariant GmbH (Germany) under the trade name Na-SKS.
  • these silicates are Na-SKS-1 (Na 2 Si 22 O 45 • x H 2 O, kenyaite), Na-SKS-2 (Na 2 Si 14 O 29 • x H 2 O, magadiite), Na-SKS -3 (Na 2 Si 8 Oi 7 .xH 2 O) or Na-SKS-4 (Na 2 Si 4 O 9 .xH 2 O, Makatite).
  • Particularly suitable for the purposes of the present invention are crystalline phyllosilicates of the formula NaMSi x O 2x + I "y H 2 O, in which x is 2.
  • Na-SKS-5 CX-Na 2 Si 2 O 5
  • Na-SKS-7 B-Na 2 Si 2 O 5 , natrosilite
  • Na-SKS-9 NaHSi 2 O 5 • H 2 O
  • Na-SKS-10 NaHSi 2 O 5 • 3 H 2 O, kanemite
  • Na-SKS-11 t-Na 2 Si 2 0 5
  • Na-SKS-13 NaHSi 2 O 5
  • Na-SKS-6 5-Na 2 Si 2 O 5 .
  • these means preferably contain a weight proportion of crystalline layered silicate of the formula NaMSi x O 2x + 1 ⁇ y H 2 O from 0.1 to 20 wt .-%, from 0.2 to 15 wt .-% and in particular from 0.4 to 10 wt .-%, each based on the total weight of these agents.
  • Such automatic dishwashing agents have a total silicate content of less than 7% by weight, preferably less than 6% by weight, preferably less than 5% by weight, more preferably less than 4% by weight, most preferably less than 3% by weight % and in particular below 2.5 wt .-%, wherein it is in this silicate, based on the total weight of the silicate contained, preferably at least 70 wt .-%, preferably at least 80 wt .-% and in particular to At least 90 wt .-% of silicate of the general formula NaMSi x O 2x + - I • y H 2 O is.
  • amorphous sodium silicates with a Na 2 O: SiO 2 modulus of from 1: 2 to 1: 3.3, preferably from 1: 2 to 1: 2.8 and in particular from 1: 2 to 1: 2.6, which Delayed and have secondary washing properties.
  • the dissolution delay compared with conventional amorphous sodium silicates may have been caused in various ways, for example by surface treatment, compounding, compaction / densification or by overdrying.
  • the term "amorphous” is also understood to mean "X-ray amorphous”.
  • the silicates do not yield sharp X-ray reflections typical of crystalline substances in X-ray diffraction experiments, but at most one or more maxima of the scattered X-rays which have a width of several degrees of diffraction angle. However, it may well even lead to particularly good builder properties if the silicate particles provide blurred or even sharp diffraction maxima in electron diffraction experiments. This is to be interpreted as meaning that the products have microcrystalline regions of the size of ten to a few hundred nm, with values of up to max. 50 nm and in particular up to max. 20 nm are preferred. Such so-called X-ray amorphous silicates also have a dissolution delay compared with the conventional water glasses.
  • compacted / compacted amorphous silicates particularly preferred are compacted / compacted amorphous silicates, compounded amorphous silicates and overdried X-ray amorphous silicates.
  • these (s) silicate (s) preferably alkali metal silicates, particularly preferably crystalline or amorphous Alkalidisilikate, in amounts of 10 to 60 wt .-%, preferably from 15 to 50 wt .-% and in particular from 20 to 40% by weight, based in each case on the weight of the detergency booster.
  • alkali carriers are, for example, alkali metal hydroxides, alkali metal carbonates, alkali metal hydrogencarbonates, alkali metal sesquicarbonates, the alkali silicates mentioned, alkali metal silicates, and mixtures of the abovementioned substances, preference being given to using alkali metal carbonates, in particular sodium carbonate, sodium bicarbonate or sodium sesquicarbonate for the purposes of this invention.
  • alkali metal carbonates in particular sodium carbonate, sodium bicarbonate or sodium sesquicarbonate for the purposes of this invention.
  • a builder system comprising a mixture of tripolyphosphate and sodium carbonate.
  • a builder system comprising a mixture of tripolyphosphate and sodium carbonate and sodium disilicate.
  • the alkali metal hydroxides are preferred in the Waschkraftverstäreker only in small amounts, preferably in amounts below 30 wt .-%, preferably below 20 wt .-%, more preferably below 15 wt .-% and in particular below 12 wt .-%, each based on the total weight of the washing power amplifier used.
  • carbonate (s) and / or bicarbonate (s) preferably alkali metal carbonate (s), more preferably sodium carbonate
  • organic co-builders are polycarboxylates / polycarboxylic acids, polymeric polycarboxylates, aspartic acid, polyacetals, dextrins, other organic cobuilders (see below) and phosphonates. These classes of substances are described below.
  • Useful organic builder substances are, for example, the polycarboxylic acids which can be used in the form of their sodium salts, polycarboxylic acids meaning those carboxylic acids which carry more than one acid function. These are, for example, citric acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, nitrilotriacetic acid (NTA), if such use is not objectionable for ecological reasons, and mixtures of these.
  • Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures thereof.
  • the acids themselves can also be used.
  • the acids typically also have the property of an acidifying component and serve thus also for setting a lower and milder pH of detergents or cleaners.
  • citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any desired mixtures of these can be mentioned here.
  • polymeric polycarboxylates for example the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example those having a relative molecular mass of 500 to 70,000 g / mol.
  • the molecular weights stated for polymeric polycarboxylates are weight-average molar masses M w of the particular acid form, which were determined in principle by means of gel permeation chromatography (GPC), a UV detector being used. The measurement was carried out against an external polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship with the polymers investigated. These data differ significantly from the molecular weight data, in which polystyrene sulfonic acids are used as standard. The molar masses measured against polystyrenesulfonic acids are generally significantly higher than the molecular weights specified in this document.
  • Suitable polymers are, in particular, polyacrylates which preferably have a molecular weight of 2,000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates, which have molar masses of from 2000 to 10000 g / mol, and particularly preferably from 3000 to 5000 g / mol, may again be preferred from this group.
  • copolymeric polycarboxylates in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid.
  • Copolymers of acrylic acid with maleic acid which contain 50 to 90% by weight of acrylic acid and 50 to 10% by weight of maleic acid have proven to be particularly suitable.
  • Their relative molecular weight, based on free acids is generally from 2000 to 70000 g / mol, preferably from 20,000 to 50,000 g / mol and in particular from 30,000 to 40,000 g / mol.
  • the (co) polymeric polycarboxylates can be used either as a powder or as an aqueous solution.
  • the content of detergents or cleaners to (co) polymeric polycarboxylates is preferably 0.5 to 20 wt .-%, in particular 3 to 10 wt .-%.
  • the polymers may also contain allylsulfonic acids such as allyloxybenzenesulfonic acid and methallyisulfonic acid as a monomer.
  • allylsulfonic acids such as allyloxybenzenesulfonic acid and methallyisulfonic acid
  • biodegradable polymers of more than two different monomer units for example those which contain as monomers the salts of acrylic acid and maleic acid and vinyl alcohol or vinyl alcohol derivatives or the salts of acrylic acid and 2-alkylacrylic sulfonic acid as monomers. Derivatives included.
  • copolymers are those which preferably have as monomers acrolein and acrylic acid / acrylic acid salts or acrolein and vinyl acetate.
  • polymeric aminodicarboxylic acids their salts or their precursors. Particular preference is given to polyaspartic acids or their salts.
  • the detergency booster contains a builder, preferably in amounts above 10 wt .-%, preferably above 20 wt .-% and in particular above 40 wt .-%, according to the invention are preferred.
  • the detergency booster contains a chlorine bleach or bromine bleach.
  • Suitable chlorine- or bromine-releasing materials include heterocyclic N-bromo and N-chloroamides, for example, trichloroisocyanuric acid, Tribromisocyanu 'rklare, dibromoisocyanuric and / or
  • the content of the detergency booster to chlorine or bromine bleaches is preferably between 0.1 and 30 wt .-%, preferably between 0.2 and 25 wt .-%, particularly preferably between 0.4 and 20 wt .-% and in particular between 0 , 8 and 15 wt .-%.
  • the chlorine or bromine bleach-containing detergency booster are preferably formulated in liquid form.
  • the detergency booster may contain an oxygen bleach.
  • Preferred combination products are characterized in that the detergency booster contains an oxygen bleach.
  • oxygen bleach is a compound serving as bleaches in water H 2 O 2 .
  • sodium percarbonate, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance.
  • Other useful bleaching agents are, for example, peroxypyrophosphates, citrate perhydrates and H 2 O 2 -forming peracidic salts or peracids, such as perbenzoates, peroxophthalates, diperazelaic acid, phthaloiminoperacid or diperdodecanedioic acid.
  • bleaching agents from the group of organic bleaching agents can also be used.
  • Typical organic bleaches are the diacyl peroxides such as dibenzoyl peroxide.
  • Other typical organic Bleaching agents are the peroxyacids, with particular mention being made of the alkylperoxyacids and the arylperoxyacids.
  • Preferred representatives are (a) the peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, but also peroxy- ⁇ -naphthoic acid and magnesium monoperphthalate, (b) the aliphatic or substituted aliphatic peroxyacids, such as peroxylauric acid, peroxystearic acid, ⁇ -phthalimidoperoxycaproic acid
  • PAP Phthaliminoperoxyhexanoic acid
  • o-carboxybenzamidoperoxycaproic acid N-nonenylamidoperadipic acid and N-nonenylamidopersuccinate
  • aliphatic and araliphatic peroxydicarboxylic acids such as 1,12-diperoxycarboxylic acid, 1,9-diperoxyazelaic acid, diperoxysebacic acid, diperoxybrassic acid, the diperoxyphthalic acids, 2- Decyldiperoxybutane-1,4-diacid, N, N-terephthaloyl-di (6-aminopercapronate) can be used.
  • the detergency enhancers include dibenzoyl peroxide and / or sodium percarbonate.
  • the content of the detergency booster in oxygen bleaching agents is preferably between 0.1 and 30% by weight, preferably between 0.2 and 25% by weight, more preferably between 0.4 and 20% by weight and in particular between 0.8 and 15% by weight.
  • the oxygen bleach-containing detergency boosters are preferably formulated in liquid form or in the form of particulate compositions.
  • the average particle size of these particulate compositions is preferably between 100 and 5000 microns, more preferably between 100 and 2000 microns, and in particular between 100 and 1000 microns.
  • Combination products characterized in that the detergency booster contains a bleaching agent, preferably in amounts above 10% by weight, preferably above 20% by weight and in particular above 40% by weight, are preferred according to the invention.
  • the washing power intensifier contained in the combination product according to the invention unfolds its effect in the pre-rinse cycle of the automatic dishwashing process, wherein the detergency booster is preferably consumed to the greatest possible extent, that is, in the aqueous liquor in solution or disperses. Preference is given to those detergency boosters which consume at least 30% by weight, preferably at least 50% by weight, preferably at least 60% by weight and in particular at least 80% by weight, in the prewash cycle.
  • Combination product characterized in that the washing power amplifier completely consumed in the course of the pre-wash cycle, are particularly preferred in the context of the present application.
  • the term "completely consumed” means a detergency booster whose contents contain less than 15% by weight, preferably less than 10% by weight, preferably less than 8% by weight, more preferably less than 6 Wt .-% and In particular, less than 3 wt .-% are abducted in the main wash cycle.
  • particularly preferred are those detergency boosters whose ingredients are taken to less than 1 wt .-% and in particular less than 0.5 wt .-% in the main wash cycle.
  • Combination products according to, characterized in that the main cleaning agent completely consumed in the course of the main rinsing, are also preferred according to the invention.
  • the term "completely consumed” therefore applies to such a main cleaning agent, of the ingredients of which less than 15% by weight, preferably less than 10% by weight, preferably less than 8% by weight, more preferably less than 6
  • particularly preferred are those main cleaning agents whose contents are less than 1 wt .-% and in particular less than 0.5 wt .-% in the Rinse cycle be towed.
  • the combination product according to the invention in addition to the detergency booster, the main cleaning agent and the instructions for use, further comprises a dosing aid.
  • Combination products characterized in that the combination product further comprises a metering aid for the detergency booster and / or for the main cleaning agent, are inventively preferred.
  • Suitable metering aids are, for example, all devices and articles which are suitable for metering the detergency booster or the main cleaning agent into the dishwasher or its metering chamber; and / or are suitable for measuring a given volume or weight.
  • Dosing aids are used with particular preference in particular for flowable detergency booster or main cleaning agent.
  • Suitable flowable agents are liquids and gels as well as particulate compositions such as powders, granules, agglomerates or extrudates.
  • Suitable dosing aids are, for example, (measuring) cups or (measuring) scoops, (measuring) spoons. These metering aids can be made for example of polymeric plastics, glass, paper or plastic.
  • Another essential component of the combination product according to the invention is the instructions for use.
  • this instruction manual is preferably contained in or on the outer packaging of the washing power booster and / or the main cleaning agent.
  • the instructions for use are printed with particular preference to the primary or secondary packaging of the washing power intensifier and / or the main cleaning agent.
  • the instructions for use guide the user to the use of the detergency booster and main detergent in the pre-rinsing and main-cleaning cycle of a machine dishwashing process.
  • the instructions for use preferably continue to give guidance on the amount of dosage, the type of dosage, the choice of cleaning program, the type of dishes to be cleaned (eg glass, porcelain, plastic, wood, etc.) and the type of possibly in combination with the inventive combination products to be used further cleaning agents (eg deodorant, silver protection, glass protection, etc.)
  • compositions according to the invention are distinguished by an improved cleaning and rinsing action. This improved effect allows the consumer or user the choice of water and / or energy-saving machine dishwashing. For this reason, such combination products according to the invention are particularly preferred in which the instructions for use for carrying out an energy and / or water-saving machine dishwashing method leads.
  • the detergency booster show outstanding cleaning and rinsing performance especially in combination with modern "2in1" and "3in1" dishwashing detergents.
  • the combination products according to the invention therefore preferably contain a “2in1” or a “3in1” cleaning agent.
  • Combination products in which the instructions for use lead to the performance of a "2in1” or “3in1” automatic dishwashing process are therefore preferred according to the invention.
  • compositions according to the invention show their improved cleaning action especially on difficult to clean residues of glass, plastic or dishes. These residues, which are traditionally often pre-cleaned by a manual, can be removed when using the combination product according to the invention without the use of manual cleaning. Combination products in which the instructions for use to avoid manual pre-cleaning of the dishes instructs, are therefore particularly preferred according to the invention.
  • the subsequent cleaning of the items to be washed has now proven to be superfluous when using the compositions according to the invention.
  • the subject of this application is therefore an inventive combination product, characterized in that the Instructions for use to dispense with a subsequent cleaning of the dishes, preferably to dispense with a manual subsequent cleaning of the dishes, instructs.
  • a further subject of this application is therefore an inventive combination product, characterized in that the instructions for use of the combination product for cleaning metal surfaces, preferably for cleaning stainless steel surfaces, or for cleaning enamel surfaces or for cleaning scratch-resistant coated surfaces, preferably surfaces made of Teflon ® instructs.
  • the mixtures preferably have predominantly oxidic composition and are particularly preferably based on a glass matrix, preferably an alkali borosilicate matrix, in which opacifiers and coloring ceramic pigments are dispersed.
  • the combination products according to the invention have an effect, in particular, against tea contaminants and against burnt-in soils, such as fatty encrustations, baked minced meat or baked cheese.
  • Claimed therefore continues to be a combination product according to the invention, characterized in that the instructions for use for the purification of Teeverschmutzieux, or burnt contaminants such as fatty encrustations, burned minced meat or baked cheese instructs.
  • a further subject of the present application is a machine dishwashing method using one of the above-described combination product according to the invention, comprising the steps of a) reading an instruction manual which instructs the user to use the washing power booster in the pre-wash cycle and to use the main detergent in the main wash cycle of a machine dishwashing process; b) introducing a washing power booster into the pre-rinsing cycle of a machine dishwashing process; c) introducing a main cleaning agent into the main rinse of a machine dishwashing process.
  • the washing power booster unfolds its effect in the pre-rinse cycle of the automatic dishwashing process.
  • Direct metering of the washing force intensifier into the interior of the dishwasher has proved to be particularly advantageous for the effect of the washing force intensifier.
  • Machine dishwashing processes characterized in that the washing power booster, preferably manually, is metered into the interior of the dishwasher, are particularly preferred.
  • a further subject of this application is therefore a machine dishwashing process using a combination product according to the teaching of DE 102004051560.3, comprising the steps of a) reading an instruction manual which instructs the user to use the washing power booster in the pre-wash cycle and to use the main cleaning agent in the main rinse cycle of a machine dishwashing process; b) dosing a washing force booster on the inside of the dishwasher door; c) introducing a main cleaning agent into the main rinse of a machine dishwashing process.
  • the detergency boosters are particularly characterized by improved cleaning and rinse results in combination with a "2in1" or "3in1" main detergent.
  • Such agents are dosed as well as the known dishwashing powder usually through the metering chamber.
  • Machinery Dishwashing processes in which the main cleaning agent, preferably manually, is metered into the metering chamber of the dishwasher, are particularly preferred.
  • the above-described combination products of detergency booster and Hauptinstitutsmittei contain washing and cleaning active substances, preferably washing and cleaning active substances from the group of builders, surfactants, polymers, bleach, bleach activators, enzymes, glass corrosion inhibitors, corrosion inhibitors, Disintegrationstosstoff, fragrances and perfume carriers. These preferred ingredients, unless already described, are described in greater detail below.
  • the group of surfactants includes nonionic, anionic, cationic and amphoteric surfactants.
  • nonionic surfactants it is possible to use all nonionic surfactants known to the person skilled in the art. Low-foaming nonionic surfactants are used as preferred surfactants.
  • washing or cleaning agents in particular automatic dishwashing detergents, comprise nonionic surfactants, in particular nonionic surfactants from the group of the alkoxylated alcohols.
  • the nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and on average 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol radical can be linear or preferably methyl-branched in the 2-position or linear and methyl-branched radicals in the mixture can contain, as they are usually present in Oxoalkoholresten.
  • EO ethylene oxide
  • alcohol ethoxylates with linear radicals of alcohols of natural origin having 12 to 18 carbon atoms, for example of coconut, palm, tallow or oleyl alcohol, and on average 2 to 8 moles of EO per mole of alcohol are preferred.
  • Preferred ethoxylated alcohols include, for example, Ci 2- i 4 alcohols containing 3 EO or 4 EO, C g. ir alcohol with 7 EO, C 13 .i 5 alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C 12-18 alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures from C 12-14 -AlkOhOl with 3 EO and C 12 _i ⁇ -alcohol with 5 EO.
  • the degrees of ethoxylation given represent statistical mean values which, for a specific product, may correspond to an integer or a fractional number.
  • Preferred alcohol ethoxylates have a narrow homology distribution (narrow rank ethoxylates, NRE).
  • fatty alcohols with more than 12 EO can also be used. Examples of these are tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.
  • alkyl glycosides of the general formula RO (G) x can be used, in which R is a primary straight-chain or methyl branched, in particular in the 2-position methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol which is for a glycose unit with 5 or 6 C-atoms, preferably glucose.
  • the degree of oligomerization x which indicates the distribution of monoglycosides and oligoglycosides, is an arbitrary number between 1 and 10; preferably x is 1, 2 to 1, 4.
  • nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably having from 1 to 4 carbon atoms in the alkyl chain.
  • Nonionic surfactants of the amine oxide type for example N-cocoalkyl-N, N-dimethylamine oxide and N-tallowalkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides may also be suitable.
  • the amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, especially not more than half thereof.
  • surfactants are polyhydroxy fatty acid amides of the formula
  • R is an aliphatic acyl radical having 6 to 22 carbon atoms
  • R 1 is hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms
  • [Z] is a linear or branched polyhydroxyalkyl radical having 3 to 10 carbon atoms and 3 to 10 hydroxyl groups.
  • the polyhydroxy fatty acid amides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.
  • the group of polyhydroxy fatty acid amides also includes compounds of the formula
  • R is a linear or branched alkyl or alkenyl radical having 7 to 12 carbon atoms
  • R 1 is a linear, branched or cyclic alkyl radical or an aryl radical having 2 to 8 carbon atoms
  • R 2 is a linear, branched or cyclic Alkyl radical or an aryl radical or an oxy-alkyl radical having 1 to 8 carbon atoms, wherein C- M alkyl or phenyl radicals are preferred and [Z] is a linear polyhydroxyalkyl radical whose alkyl chain is substituted with at least two hydroxyl groups, or alkoxylated, preferably ethoxylated or propoxylated derivatives of this group.
  • [Z] is preferably obtained by reductive amination of a reduced sugar, for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • a reduced sugar for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • the N-alkoxy- or N-aryloxy-substituted compounds can be converted into the desired polyhydroxy fatty acid amides by reaction with fatty acid methyl esters in the presence of an alkoxide as catalyst.
  • surfactants are further used which contain one or more Taigfettalkohole with 20 to 30 EO in combination with a silicone defoamer.
  • Nonionic surfactants from the group of alkoxylated alcohols are also used with particular preference.
  • Nonionic surfactants which have a melting point above room temperature.
  • Suitable nonionic surfactants which have melting or softening points in the temperature range mentioned are, for example, low-foaming nonionic surfactants which may be solid or highly viscous at room temperature. If nonionic surfactants are used which are highly viscous at room temperature, it is preferred that they have a viscosity above 20 Pa ⁇ s, preferably above 35 Pa ⁇ s and in particular above 40 Pa ⁇ s. Nonionic surfactants which have waxy consistency at room temperature are also preferred.
  • surfactants which are solid at room temperature, come from the groups of alkoxylated nonionic surfactants, in particular the ethoxylated primary alcohols and mixtures of these surfactants with structurally complicated surfactants such as polyoxypropylene / Poiyoxyethylen / polyoxypropylene ((PO / EO / PO) surfactants).
  • Such (PO / EO / PO) nonionic surfactants are also characterized by good foam control.
  • the nonionic surfactant having a melting point above room temperature is an ethoxylated nonionic surfactant derived from the Reaction of a monohydroxyalkanol or alkylphenol having 6 to 20 carbon atoms with preferably at least 12 mol, more preferably at least 15 moles, in particular at least 20 moles of ethylene oxide per mole of alcohol or alkylphenol emerged.
  • a particularly preferred room temperature solid nonionic surfactant is obtained from a straight chain fatty alcohol having 16 to 20 carbon atoms (C 16-20 alkoxy), preferably a C 18 alcohol and at least 12 moles, preferably at least 15 moles and especially at least 20 moles of ethylene oxide.
  • C 16-20 alkoxy a straight chain fatty alcohol having 16 to 20 carbon atoms
  • C 18 alcohol preferably a C 18 alcohol and at least 12 moles, preferably at least 15 moles and especially at least 20 moles of ethylene oxide.
  • the so-called “narrow rank ethoxylates” are particularly preferred.
  • ethoxylated nonionic surfactants which consist of C 6-20 -monohydroxyalkanols or C 6-20 -alkylphenols or C 16-20 -fatty alcohols and more than 12 mol, preferably more than 15 mol and in particular more than 20 mol of ethylene oxide per Mol of alcohol were used.
  • the nonionic surfactant solid at room temperature preferably additionally has propylene oxide units in the molecule.
  • such PO units make up to 25 wt .-%, more preferably up to 20 wt .-% and in particular up to 15 wt .-% of the total molecular weight of the nonionic surfactant from.
  • Particularly preferred nonionic surfactants are ethoxylated monohydroxyalkanols or alkylphenols which additionally have polyoxyethylene-polyoxypropylene block copolymer units.
  • the alcohol or alkylphenol part of such nonionic surfactant molecules preferably constitutes more than 30% by weight, more preferably more than 50% by weight and in particular more than 70% by weight of the total molecular weight of such nonionic surfactants.
  • Preferred agents are characterized in that they contain ethoxylated and propoxylated nonionic surfactants, in which the propylene oxide units in the molecule up to 25 wt .-%, preferably up to 20 wt .-% and in particular up to 15 wt .-% of the total molecular weight of the nonionic Make up surfactants.
  • nonionic surfactants having melting points above room temperature contain from 40 to 70% of a polyoxypropylene / polyoxyethylene / polyoxypropylene block polymer blend containing 75% by weight of a reverse block copolymer of polyoxyethylene and polyoxypropylene with 17 moles of ethylene oxide and 44 moles of propylene oxide and 25% by weight.
  • Non-ionic surfactants that can be used with particular preference are available, for example, under the name Poly Tergent ® SLF-18 from Olin Chemicals. Surfactants of the formula
  • R 1 is a linear or branched aliphatic hydrocarbon radical having 4 to 18 carbon atoms or mixtures thereof
  • R 2 denotes a linear or branched hydrocarbon radical having 2 to 26 carbon atoms or mixtures thereof and x for values between 0.5 and 1.5 and y is a value of at least 15 are further particularly preferred nonionic surfactants.
  • nonionic surfactants are the end-capped poly (oxyalkylated) nonionic surfactants of the formula
  • R 1 and R 2 are 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, iso-propyl, n- Butyl, 2-butyl or 2-methyl-2-butyl radical
  • x are values between 1 and 30, k and j are 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 0R 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, with radicals having 8 to 18 carbon atoms being particularly preferred.
  • R 3 H, -CH 3 or -CH 2 CH 3 are particularly preferred.
  • 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 may be different if x ⁇ 2.
  • the alkylene oxide unit in the square bracket can be varied.
  • the value 3 for x has been selected here by way of example and may well be greater, 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 is 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 is H and x assumes values of 6 to 15.
  • end-capped poly (oxyalkylated) nonionic surfactants are of the formula
  • R 1 and R 2 are 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, iso-propyl, n- Butyl, 2-butyl or 2-methyl-2-butyl radical
  • x are values between 1 and 30
  • k and j are values between 1 and 12, preferably between 1 and 5, preference being given to surfactants of the type
  • x is from 1 to 30, preferably from 1 to 20 and in particular from 6 to 18, are particularly preferred.
  • nonionic surfactants have been low foaming nonionic surfactants which have alternating ethylene oxide and alkylene oxide units.
  • surfactants with EO-AO-EO-AO blocks are preferred, wherein in each case one to ten EO or AO groups are bonded to each other before a block of the other groups follows.
  • R 1 is a straight-chain or branched, saturated or mono- or polyunsaturated C 6-24 alkyl or alkenyl radical; each group R 2 or R 3 independently is selected from -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 -CH 3 , CH (CH 3 ) 2 and the indices w, x, y, 2 independently of one another are integers from 1 to 6.
  • the preferred nonionic surfactants of the above formula can be prepared by known methods from the corresponding alcohols R 1 -OH and ethylene or alkylene oxide.
  • the radical R 1 in the above formula may vary depending on the origin of the alcohol. If native sources are used, the radical R 1 has an even number of carbon atoms and is usually unbranched, the linear radicals being selected from alcohols of natural origin having 12 to 18 C atoms, for example from coconut, palm, tallow or Oleyl alcohol, are preferred. Examples of alcohols which are accessible from synthetic sources are the Guerbet alcohols or methyl-branched or linear and methyl-branched radicals in the 2-position, such as are usually present in oxo alcohol radicals.
  • nonionic surfactants in which R 1 in the above formula is an alkyl radical having 6 to 24, preferably 8 to 20, particularly preferably 9 to 15 and in particular 9 to 11 Carbon atoms.
  • alkylene oxide unit which is contained in the preferred nonionic surfactants in alternation with the ethylene oxide unit, in particular butylene oxide is considered in addition to propylene oxide.
  • R 2 or R 3 are independently selected from - CH 2 CH 2 -CH 3 or CH (CH 3 ) 2 are suitable.
  • nonionic surfactants which have a C 9 . 15 alkyl 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.
  • These surfactants have the required low viscosity in aqueous solution and can be used according to the invention with particular preference.
  • nonionic surfactants are the end-capped poly (oxyalkylated) nonionic surfactants of the formula
  • R 1 represents linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms
  • R 2 represents linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, which preferably between 1 and 5 hydroxy groups and preferably further functionalized with an ether group
  • R 3 is H or a methyl, ethyl, n-propyl, iso-propyl, n-butyl, 2-butyl or 2-methyl-2-butyl radical and x is values between 1 and 40
  • R 3 in the abovementioned general formula is H.
  • R 1 is linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, preferably having 4 to 20 carbon atoms
  • R 2 is linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, which preferably have between 1 and 5 hydroxyl groups and x stands for values between 1 and 40.
  • radical R 1 which is linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, preferably having 4 to 20 carbon atoms, furthermore a linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radical R 2 having 1 to 30 carbon atoms R 2 , which is a monohydroxylated intermediate group - CH 2 CH (OH) - adjacent.
  • x in this formula stands for values between 1 and 90.
  • radical R 1 which in addition to a radical R 1 , which is linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, preferably having 4 to 22 carbon atoms, further a linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radical R 2 having 1 to 30 carbon atoms, preferably 2 to 22 carbon atoms, which has a monohydroxylated intermediate group -CHaCH (OH) - and in which x stands for values between 40 and 80, preferably for values between 40 and 60.
  • R 1 which is linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radicals having 1 to 30 carbon atoms, preferably having 4 to 22 carbon atoms, further a linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon radical R 2 having 1 to 30 carbon atoms, preferably 2 to 22 carbon atoms, which has a monohydroxylated intermediate group -CHaCH (
  • the corresponding end-capped poly (oxyalkylated) nonionic surfactants of the above formula can be prepared, for example, by reacting a terminal epoxide of the formula R 2 CH (O) CH 2 with an ethoxylated alcohol of the formula R 1 O [CH 2 CH 2 O] x-1 CH 2 Obtained CH 2 OH.
  • R 1 and R 2 independently of one another are a linear or branched, saturated or mono- or polyunsaturated hydrocarbon radical having 2 to 26 carbon atoms
  • R 3 is independently selected from -CH 3 -CH 2 CH 3 , -CH 2 CH 2 -CH 3 , CH (CH 3 ) 2 , but preferably -CH 3
  • x and y are independently of one another values between 1 and 32, nonionic surfactants having values for x of 15 to 32 and y of 0, 5 and 1, 5 are very particularly preferred.
  • R 1 and R 2 independently of one another are a linear or branched, saturated or mono- or polyunsaturated hydrocarbon radical having 2 to 26 carbon atoms
  • R 3 is independently selected from -CH 3 -CH 2 CH 3 , -CH 2 CH 2 -CH 3 , CH (CH 3 ) 2 , but preferably represents -CH 3
  • x and y independently of one another are values between 1 and 32 are preferred according to the invention, wherein nonionic surfactants with values of x from 15 to 32 and y of 0.5 and 1.5 are very particularly preferred.
  • the stated C chain lengths and degrees of ethoxylation or degrees of alkoxylation of the abovementioned nonionic surfactants represent statistical mean values which, for a specific product, may be an integer or a fractional number. Due to the production process, commercial products of the formulas mentioned are usually not composed of an individual representative but of mixtures, which results in both the C chain lengths and the ethoxy Al michellessgrade or Alkoxyl michsgrade mean values and resulting in broken numbers.
  • nonionic surfactants can be used not only as individual substances, but also as surfactant mixtures of two, three, four or more surfactants.
  • Mixtures of surfactants are not mixtures of nonionic surfactants which fall in their entirety under one of the abovementioned general formulas, but rather mixtures which contain two, three, four or more nonionic surfactants which can be described by different general formulas ,
  • anionic surfactants for example, those of the sulfonate type and sulfates are used.
  • the surfactants of the sulfonate type are preferably C 9 . 13- Alkylbenzolsul- fonates, olefinsulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates, as obtained for example from Ci 2- i 8 monoolefins having terminal or internal double bond by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation , considering.
  • alkanesulfonates which are for example derived from C 12-i 8 alkanes by sulfochlorination or sulfoxidation and subsequent hydrolysis or neutralization.
  • esters of ⁇ -sulfo fatty acids for example, the ⁇ -sulfonated methyl esters of hydrogenated coconut, palm kernel or Taigfettcicren are suitable.
  • sulfated fatty acid glycerol esters are to be understood as meaning the mono-, di- and triesters and mixtures thereof, as obtained in the preparation by esterification of a monoglycerol with 1 to 3 moles of fatty acid or in the transesterification of triglycerides with 0.3 to 2 moles of glycerol.
  • Preferred sulfated fatty acid glycerol esters are the sulfonation products of saturated fatty acids containing 6 to 22 carbon atoms, for example caproic acid, caprylic acid, capric acid, myristic acid, lauric acid, palmitic acid, stearic acid or behenic acid.
  • Alk (en) yl sulfates are the alkali and especially the sodium salts of Schwefelklareschester the C 12 -C 18 fatty alcohols, for example coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol, or C 10 -C 2 o Oxo alcohols and those half-esters of secondary alcohols of these chain lengths are preferred. Also preferred are alk (en) ylsulfates of said chain length, which contain a synthetic, produced on a petrochemical basis straight-chain alkyl radical, which have an analogous degradation behavior as the adequate compounds based on oleochemical raw materials.
  • C 12 -C 16 alkyl sulfates and C 12 -C 15 - Alkyl sulfates and C 14 -C 5 alkyl sulfates are preferred.
  • 2,3-AlkyIsulfate which can be obtained as commercial products from Shell Oil Company under the name DAN ®, are suitable anionic surfactants.
  • 2 i-alcohols such as 2-methyl-branched C 9 . ir alcohols containing on average 3.5 mol ethylene oxide (EO) or C 12-i 8 fatty alcohols containing 1 to 4 EO, are also suitable. Due to their high foaming behavior, they are only used in detergents in relatively small quantities, for example in amounts of from 1 to 5% by weight.
  • Suitable anionic surfactants are also the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic acid esters and which are monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • alcohols preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • Preferred sulfosuccinates contain C 8 - I8 - fatty alcohol radicals or mixtures thereof.
  • Particularly preferred sulfosuccinates contain a fatty alcohol residue derived from ethoxylated fatty alcohols, which by themselves are nonionic surfactants.
  • Sulfosuccinates whose fatty alcohol residues are derived from ethoxylated fatty alcohols with a narrow homolog distribution, are again particularly preferred.
  • alk (en) yl-succinic acid having preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.
  • anionic surfactants are particularly soaps into consideration.
  • Suitable are saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid, and in particular of natural fatty acids, e.g. Coconut, palm kernel or tallow fatty acids, derived soap mixtures.
  • the anionic surfactants may be in the form of their sodium, potassium or ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • the anionic surfactants are preferably present in the form of their sodium or potassium salts, in particular in the form of the sodium salts.
  • anionic surfactants are part of automatic dishwasher detergents, their content, based on the total weight of the compositions, is preferably less than 4% by weight, preferably less than 2% by weight and very particularly preferably less than 1% by weight. Machine dishwashing detergents which do not contain anionic surfactants are particularly preferred.
  • cationic active substances for example, cationic compounds of the following formulas can be used:
  • the content of cationic and / or amphoteric surfactants is preferably less than 6% by weight, preferably less than 4% by weight, very particularly preferably less than 2% by weight and in particular less than 1% by weight. %. Automatic dishwashing detergents containing no cationic or amphoteric surfactants are particularly preferred.
  • the group of polymers includes, in particular, the washing or cleaning-active polymers, for example the rinse aid polymers and / or polymers which act as softeners.
  • the washing or cleaning-active polymers for example the rinse aid polymers and / or polymers which act as softeners.
  • cationic, anionic and amphoteric polymers can be used in detergents or cleaners in addition to nonionic polymers.
  • “Cationic polymers” in the context of the present invention are polymers which carry a positive charge in the polymer molecule, which can be carried out, for example, in the polymer chain present (alkyl) ammonium groups or other positively charged groups can be realized.
  • Particularly preferred cationic polymers come from the groups of quaternized cellulose derivatives, the polysiloxanes with quaternary groups, the cationic guar derivatives, the polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid, the copolymers of vinylpyrrolidone with quaternized derivatives of dialkylamino and methacrylates, the vinylpyrrolidone-methoimidazolinium chloride copolymers, the quaternized polyvinyl alcohols or the polymers specified under the INCI names Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and Polyquaternium 27.
  • amphoteric polymers further comprise, in addition to a positively charged group in the polymer chain, also negatively charged groups or monomer units. These groups may be, for example, carboxylic acids, sulfonic acids or phosphonic acids.
  • particularly preferred cationic or amphoteric polymers contain as monomer unit a compound of the general formula
  • R 1 and R 4 are each independently H or a linear or branched hydrocarbon radical having 1 to 6 carbon atoms;
  • R 2 and R 3 independently of one another are an alkyl, hydroxyalkyl, or aminoalkyl group in which the alkyl radical is linear or is branched and has between 1 and 6 carbon atoms, which is preferably a methyl group;
  • x and y independently represent integers between 1 and 3.
  • X " represents a counterion, preferably a counterion from the group consisting of chloride, bromide, iodide, sulfate, hydrogensulfate, methosulfate, lauryl sulfate, dodecylbenzenesulfonate, p-toluenesulfonate (tosylate), cumene sulfonate, xylenesulfonate, phosphate, citrate, formate, acetate or mixtures thereof.
  • Preferred radicals R 1 and R 4 in the above formula are selected from -CH 3, -CH 2 -CH 3, - CH 2 -CH 2 -CH 3, -CH (CHs) -CH 3, -CH 2 -OH, -CH 2 -CH 2 -OH, -CH (OH) -CH 3 , -CH 2 -CH 2 -CH 2 -OH, -CH 2 -CH (OH) -CH 3 , -CH (OH) -CH 2 -CH 3 , and - (CH 2 CH 2 -O) n H.
  • cationic or amphoteric polymers contain a monomer unit of the general formula
  • R1 HC C Rz-C (O) -NH- (CH 2) - RsRtRs + N
  • X " in the R 1 , R 2 , R 3 , R 4 and R 5 are independently of one another a linear or branched, saturated or unsaturated alkyl or hydroxyalkyl radical having 1 to 6 carbon atoms, preferably a linear or branched alkyl radical selected from CH 3 , -CH 2 -CH 3 , - CH 2 -CH 2 -CH 3 , -CH (CH 3 ) -CH 3 , -CH 2 -OH, -CH 2 -CH 2 -OH, -CH (OH) -CH 3 , -CH 2 -CH 2 -CH 2 -OH, -CH 2 - CH (OH) -CH 3 , -CH (OH) -CH 2 -CH 3 , and - (CH 2 CH 2 -O) n is H and x is an integer between 1 and 6.
  • H 2 C C (CH 3 ) -C (O) -NH- (CH 2) ⁇ -N + (CH 3 ) 3
  • X " chloride also referred to as MAPTAC (Methyacrylamidopropyl- trimethylammonium chloride).
  • amphoteric polymers have not only cationic groups but also anionic groups or monomer units.
  • anionic monomer units are derived, for example, from the group of linear or branched, saturated or unsaturated carboxylates, linear or branched, saturated or unsaturated phosphonates, linear or branched, saturated or unsaturated sulfates or linear or branched, saturated or unsaturated sulfonates.
  • Preferred monomer units are acrylic acid, (meth) acrylic acid, (dimethyl) acrylic acid, (ethyl) acrylic acid, cyanoacrylic acid, vinylic acid, allylacetic acid, crotonic acid, maleic acid, fumaric acid, cinnamic acid and their derivatives, which Allylsulfonic acids such as allyloxybenzenesulfonic acid and methallylsulfonic acid or the allylphosphonic acids.
  • Preferred usable amphoteric polymers are selected from the group of the alkylacrylamide / acrylic acid copolymers, the alkylacrylamide / methacrylic acid copolymers, the alkylacrylamide / methylmethacrylic acid copolymers, the alkylacrylamide / acrylic acid / alkylaminoalkyl (meth) acrylic acid copolymers, the
  • Preferably usable zwitterionic polymers are selected from the group of acrylamidoalkyltrialkylammonium chloride / acrylic acid copolymers and their alkali metal and Ammonium salts, the acrylamidoalkyltrialkylammonium chloride / methacrylic acid copolymers and their alkali metal and ammonium salts and the Methacroylethylbetain / methacrylate copolymers.
  • amphoteric polymers which comprise, in addition to one or more anionic monomers as cationic monomers, methacrylamidoalkyltrialkylammonium chloride and dimethyl (diallyl) ammonium chloride.
  • amphoteric polymers come from the group of Methacrylamidoalkyl- trialkylammonium chloride / dimethyl (diallyl) ammonium chloride / acrylic acid copolymers, the
  • amphoteric polymers from the group of:
  • the polymers are present in prefabricated form.
  • Coating compositions preferably by means of water-soluble or water-dispersible natural or synthetic polymers; the encapsulation of the polymers by means of water-insoluble, fusible
  • Coating composition preferably by means of water-insoluble coating agent from the
  • Support materials from the group of washing or cleaning-active substances particularly preferably from the group of builders (builders) or cobuilders.
  • Detergents or cleaning agents contain the aforementioned cationic and / or amphoteric polymers preferably in amounts of between 0.01 and 10 wt .-%, each based on the total weight of the detergent or cleaning agent.
  • Effective polymers as softeners are, for example, the sulfonic acid-containing polymers which are used with particular preference.
  • sulfonic acid-containing polymers are copolymers of unsaturated carboxylic acids, sulfonic acid-containing monomers and optionally other ionic or nonionic monomers.
  • R 1 to R 3 independently of one another, are -H, -CH 3 , a straight-chain or branched saturated alkyl radical having 2 to 12 carbon atoms, a straight-chain or branched, mono- or polyunsaturated alkenyl radical having 2 to 12 carbon atoms, NH 2 , -OH or -COOH substituted alkyl or alkenyl radicals or -COOH or -COOR 4 , wherein R 4 is a saturated or unsaturated, straight-chain or branched hydrocarbon radical having 1 to 12 carbon atoms.
  • Preferred among these monomers are those of the formulas
  • 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-hydroxypropanesulfonic acid, allylsulfonic acid, methallylsulfonic acid, allyloxybenzenesulfonic acid, methallyloxybenzenesulfonic acid, 2-hydroxy-3- (2-propenyloxy) propanesulfonic acid, 2-methyl-2-propenylsulfonic acid, styrenesulfonic acid, vinylsulfonic acid, 3-sulfopropyl acrylate, 3-sulfopropyl methacrylate , Sulfomethacrylamide, sulfomethylmethacrylamide and water-soluble salts of said acids.
  • Particularly suitable other ionic or nonionic monomers are ethylenically unsaturated compounds.
  • the content of the polymers used in these other ionic or nonionic monomers is preferably less than 20% by weight, based on the polymer.
  • copolymers consist of i) one or more unsaturated carboxylic acids from the group of acrylic acid,
  • the copolymers may contain the monomers from groups i) and ii) and, if appropriate, iii) in varying amounts, it being possible for all representatives from group i) to be combined with all representatives from group ii) and all representatives from group iii).
  • Particularly preferred polymers have certain structural units, which are described below.
  • copolymers which are structural units of the formula are preferred.
  • These polymers are prepared by copolymerization of acrylic acid with a sulfonic acid-containing acrylic acid derivative.
  • acrylic acid derivative containing sulfonic acid groups is copolymerized with methacrylic acid, another polymer is obtained whose use is likewise preferred.
  • the corresponding copolymers contain the structural units of the formula
  • Acrylic acid and / or methacrylic acid can also be copolymerized completely analogously with methacrylic acid derivatives containing sulfonic acid groups, as a result of which the structural units in the molecule are changed.
  • acrylic acid and / or methacrylic acid or in addition thereto maleic acid can also be used as a particularly preferred monomer from group i). This gives way to inventively preferred copolymers, the structural units of the formula
  • the sulfonic acid groups may be wholly or partly in neutralized form, ie that the acidic acid of the sulfonic acid group in some or all sulfonic acid groups may be exchanged for metal ions, preferably alkali metal ions and especially sodium ions.
  • metal ions preferably alkali metal ions and especially sodium ions.
  • the monomer distribution of the copolymers preferably used according to the invention in the case of copolymers which contain only monomers from groups i) and ii) is preferably in each case from 5 to 95% by weight i) or ii), particularly preferably from 50 to 90% by weight monomer from group i) and from 10 to 50% by weight of monomer from group ii), in each case based on the polymer.
  • terpolymers particular preference is given to those containing from 20 to 85% by weight of monomer from group i), from 10 to 60% by weight of monomer from group ii) and from 5 to 30% by weight of monomer from group iii) ,
  • the molar mass of the sulfo copolymers preferably used according to the invention can be varied in order to adapt the properties of the polymers to the desired end use.
  • Preferred washing or cleaning agents are characterized in that the copolymers have molar masses of 2000 to 200,000 gmol "1 , preferably from 4000 to 25,000 gmol " 1 and in particular from 5000 to 15,000 gmol "1 .
  • Bleach activators are used in detergents or cleaners, for example, to achieve an improved bleaching effect when cleaning at temperatures of 60 0 C and below.
  • As bleach activators it is possible to use compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups.
  • Polyacylated alkylene diamines are preferred, in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, especially 1 r 5-diacetyl-2,4-dioxohexahydro-1, 3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylglycoluril (TAGU), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate and 2,5- diacetoxy-2,5 dihydrofuran.
  • TAED tetraacetyl
  • R 2 and R 3 are independently selected from -CH 2 -CN, -CH 3 , -CH 2 -CH 3 , -CH 2 -CH 2 -CH 3 , -CH (CH 3 ) -CH 3 , -CH 2 -OH, -CH 2 -CH 2 -OH, -CH (OH) -CH 3 , -CH 2 - CH 2 -CH 2 -OH, -CH
  • bleach activators are compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups.
  • polyacylated alkylene-diamines in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular Tetraacetylglycoluril (TAGU) 1 N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate , 2,5-diacetoxy-2,5-dihydrofuran, n-methyl-morph
  • bleach activators preference is given to bleach activators from the group of the polyacylated alkylenediamines, in particular tetraacetylethylenediamine (TAED), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (US Pat.
  • TAED tetraacetylethylenediamine
  • N-acylimides in particular N-nonanoylsuccinimide (NOSI)
  • acylated phenolsulfonates in particular n-nonanoyl or isononanoyloxybenzenesulfonate
  • N- or iso-NOBS N- or iso-NOBS
  • n-methyl-morpholinium acetonitrile-methyl sulfate (MMA) preferably in amounts of up to 10 wt .-%, in particular 0.1 wt .-% to 8 wt .-%, especially 2 to 8 wt .-% and particularly preferably 2 to 6 wt .-%, each based on the total weight of the bleach activator-containing agents used.
  • bleach catalysts can also be used.
  • These substances are bleach-enhancing transition metal salts or transition metal complexes such as, for example, Mn, Fe, Co, Ru or Mo saline complexes or carbonyl complexes.
  • Mn, Fe, Co, Ru, Mo, Ti, V and Cu complexes with N-containing tripod ligands and Co, Fe, Cu and Ru ammine complexes can also be used as bleach catalysts.
  • Bleach-enhancing transition metal complexes in particular having the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, preferably selected from the group of manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (ammine) Complexes of the cobalt (acetate) complexes, the cobalt (carbonyl) complexes, the chlorides of cobalt or manganese, manganese sulfate are used in conventional amounts, preferably in an amount of up to 5 wt .-%, in particular of 0.0025 wt % to 1 wt .-% and particularly preferably from 0.01 wt .-% to 0.25 wt .-%, each based on the total weight of the bleach activator-containing agents used. But in special cases, more bleach activator can be used. enzymes
  • detergents or cleaners enzymes can be used. These include in particular proteases, amylases, lipases, hemicellulases, cellulases or oxidoreductases, and preferably mixtures thereof. These enzymes are basically of natural origin; Starting from the natural molecules, improved variants are available for use in detergents and cleaners, which are preferably used accordingly.
  • Detergents or cleaners contain enzymes preferably in total amounts of I x 10 -6 W s 5 wt .-% based on active protein. The protein concentration can be determined by known methods, for example the BCA method or the biuret method.
  • subtilisin type those of the subtilisin type are preferable.
  • subtilisins BPN 'and Carlsberg the protease PB92, the subtilisins 147 and 309, the alkaline protease from Bacillus lentus, subtilisin DY and the enzymes thermitase, proteinase K and the subtilases, but not the subtilisins in the narrower sense Proteases TW3 and TW7.
  • Subtilisin Carlsberg in a developed form under the trade names Alcalase ® from Novozymes A / S, Bagsvaard, Denmark.
  • subtilisins 147 and 309 are sold under the trade names Esperase ®, or Savinase ® from Novozymes. From the protease from Bacillus lentus DSM 5483 derived under the name BLAP ® variants are derived.
  • proteases are, for example, under the trade names Durazym ®, relase ®, Everlase® ®, Nafizym, Natalase ®, Kannase® ® and Ovozymes ® from Novozymes, under the trade names Purafect ®, Purafect ® OxP and Properase.RTM ® by the company Genencor, that under the trade name Protosol® ® from Advanced Biochemicals Ltd., Thane, India, under the trade name Wuxi ® from Firnia Wuxi Snyder Bioproducts Ltd., China, under the trade names Proleather® ® and protease P ® by the company Amano Pharmaceuticals Ltd., Nagoya, Japan, and the enzyme available under the name Proteinase K-16 from Kao Corp., Tokyo, Japan.
  • amylases which can be used according to the invention are the ⁇ -amylases from Bacillus licheniformis, from ⁇ . amyloliquefaciens or from ß. stearothermophilus and their improved for use in detergents and cleaners further developments.
  • the enzyme from B. licheniformis is available from Novozymes under the name Termamyl ® and from Genencor under the name Purastar® ® ST. Development products of this ⁇ - amylase are obtainable from Novozymes under the trade names Duramyl ® and Termamyl ® ultra, from Genencor under the name Purastar® ® OxAm and from Daiwa Seiko Inc., Tokyo, Japan as Keistase ®.
  • the ⁇ -amylase of ⁇ . amyloliquefaciens is sold by Novozymes under the name BAN ®, and derived variants from the ⁇ - amylase from B. stearothermophilus under the names BSG ® and Novamyl ®, likewise from Novozymes.
  • ⁇ -amylase from Bacillus sp. A 7-7 (DSM 12368) and the cyclodextrin glucanotransferase (CGTase) from B. agaradherens (DSM 9948).
  • lipases or cutinases are also usable according to the invention, in particular because of their triglyceride-splitting activities, but also in order to generate in situ peracids from suitable precursors.
  • lipases originally obtainable from Humicola lanuginosa (Thermomyces lanuginosus) or further developed, in particular those with the amino acid exchange D96L. They are for example marketed by Novozymes under the trade names Lipolase ®, Lipolase Ultra ®, LipoPrime® ®, Lipozyme® ® and Lipex ®.
  • the cutinases can be used, which were originally isolated from Fusarium solani pisi and Humicola insolens.
  • lipases are available from Amano under the designations Lipase CE ®, Lipase P ®, Lipase B ®, or lipase CES ®, Lipase AKG ®, Bacillis sp. Lipase® , Lipase AP® , Lipase M- AP® and Lipase AML® are available. From the company Genencor, for example, the lipases, or cutinases can be used, the initial enzymes were originally isolated from Pseudomonas mendocina and Fusarium solanii.
  • mannanases for example, under the name Gamanase ® and Pektinex AR ® from Novozymes, under the name Rohapec ® B1 from AB Enzymes and under the name Pyrolase® ® from Diversa Corp., San Diego, CA, USA available.
  • the from ß. subtilis .beta.-glucanase obtained is available under the name Cereflo ® from Novozymes.
  • Oxidoreductases for example oxidases, oxygenases, catalases, peroxidases, such as halo, chloro, bromo, lignin, glucose or manganese peroxidases, dioxygenases or laccases (phenol oxidases, polyphenooxidases) can be used according to the invention to increase the bleaching effect.
  • peroxidases such as halo, chloro, bromo, lignin, glucose or manganese peroxidases, dioxygenases or laccases (phenol oxidases, polyphenooxidases)
  • Denilite® ® 1 and 2 from Novozymes should be mentioned.
  • organic, particularly preferably aromatic, compounds which interact with the enzymes in order to enhance the activity of the relevant oxidoreductases (enhancers) or to ensure the flow of electrons (mediators) at greatly varying redox potentials between the oxidizing enzymes and the soils.
  • the enzymes originate, for example, either originally from microorganisms, such as the genera Bacillus, Streptomyces, Humicola, or Pseudomonas, and / or are produced by biotechnological methods known per se by suitable microorganisms, such as transgenic expression hosts of the genera Bacillus or filamentous fungi.
  • the purification of the relevant enzymes is preferably carried out by conventional methods, for example by precipitation, sedimentation, concentration, filtration of the liquid phases, microfiltration, ultrafiltration, exposure to chemicals, deodorization or suitable combinations of these steps.
  • the enzymes can be used in any form known in the art. These include, for example, the solid preparations obtained by granulation, extrusion or lyophilization or, especially in the case of liquid or gel-form detergents, solutions of the enzymes, advantageously as concentrated as possible, sparing in water and / or added with stabilizers.
  • the enzymes may be encapsulated for both the solid and liquid dosage forms, for example by spray-drying or extruding the enzyme solution together with a preferably natural polymer or in the form of capsules, for example those in which the enzymes are entrapped as in a solidified gel or in those of the core-shell type, in which an enzyme-containing core is coated with a water, air and / or chemical impermeable protective layer.
  • further active ingredients for example stabilizers, emulsifiers, pigments, bleaches or dyes, may additionally be applied.
  • Such capsules are prepared by methods known per se, for example by shaking or rolling granulation or in fluid-bed processes applied.
  • such granules for example by applying polymeric film-forming agent, low in dust and storage stable due to the coating.
  • a protein and / or enzyme may be particularly protected during storage against damage such as inactivation, denaturation or degradation, such as by physical influences, oxidation or proteolytic cleavage.
  • damage such as inactivation, denaturation or degradation, such as by physical influences, oxidation or proteolytic cleavage.
  • inhibition of proteolysis is particularly preferred, especially if the agents also contain proteases.
  • Detergents may contain stabilizers for this purpose; the provision of such means constitutes a preferred embodiment of the present invention.
  • One group of stabilizers are reversible protease inhibitors. Frequently, benzamidine hydrochloride, borax, boric acids, boronic acids or their salts or esters are used, including in particular derivatives with aromatic groups, such as ortho-substituted, meta-substituted and para-substituted phenylboronic acids, or their salts or esters.
  • peptidic protease inhibitors are, inter alia, ovomucoid and leupeptin to mention; An additional option is the formation of fusion proteins from proteases and peptide inhibitors.
  • enzyme stabilizers are amino alcohols such as mono-, di-, triethanol- and -propanolamine and mixtures thereof, aliphatic carboxylic acids up to C 12 , such as succinic acid, other dicarboxylic acids or salts of said acids. End-capped fatty acid amide alkoxylates are also suitable. Certain organic acids used as bulking agents are additionally capable of stabilizing a contained enzyme.
  • Lower aliphatic alcohols but especially polyols such as glycerol, ethylene glycol, propylene glycol or sorbitol are other frequently used enzyme stabilizers.
  • polyols such as glycerol, ethylene glycol, propylene glycol or sorbitol are other frequently used enzyme stabilizers.
  • calcium salts such as calcium acetate or calcium formate, and magnesium salts.
  • Polyamide oligomers or polymeric compounds such as lignin, water-soluble vinyl copolymers or cellulose ethers, acrylic polymers and / or polyamides stabilize the enzyme preparation, inter alia, against physical influences or pH fluctuations.
  • Polyamine N-oxide containing polymers act as enzyme stabilizers.
  • Other polymeric stabilizers are the linear C 8 -C 18 polyoxyalkylenes.
  • Alkyl polyglycosides can be the enzymatic components stabilize and even increase in their performance.
  • Crosslinked N-containing compounds also act as enzyme stabilizers.
  • a sulfur-containing reducing agent is, for example, sodium sulfite.
  • combinatons of stabilizers are used, for example of polyols, boric acid and / or borax, the combination of boric acid or borate, reducing salts and succinic acid or other dicarboxylic acids or the combination of boric acid or borate with polyols or polyamino compounds and with reducing salts.
  • the effect of peptide-aldehyde stabilizers is enhanced by the combination with boric acid and / or boric acid derivatives and polyols and further enhanced by the additional use of divalent cations, such as calcium ions.
  • Glass corrosion inhibitors prevent the occurrence of haze, streaks and scratches, but also iridescence of the glass surface of machine-cleaned glasses.
  • Preferred glass corrosion inhibitors come from the group of magnesium and / or zinc salts and / or magnesium and / or zinc complexes.
  • a preferred class of compounds that can be used to prevent glass corrosion are insoluble zinc salts.
  • Insoluble zinc salts in the context of this preferred embodiment are zinc salts which have a solubility of a maximum of 10 grams of zinc salt per liter of water at 20 ° C.
  • Examples of particularly preferred insoluble zinc salts according to the invention are zinc silicate, zinc carbonate, zinc oxide, basic zinc carbonate (Zn 2 (OH) 2 CO 3 ), zinc hydroxide, zinc oxalate, zinc monophosphate (Zn 3 (PO 4 ) 2 ) and zinc pyrophosphate (Zn 2 (P 2 O 7 )).
  • the zinc compounds mentioned are preferably used in amounts which have a content of the zinc ions of between 0.02 and 10% by weight, preferably between 0.1 and 5.0% by weight and in particular between 0.2 and 1.0 % By weight, based in each case on the entire glass corrosion inhibitor-containing agent.
  • Exact content of means at Zinc salt or zinc salts is naturally dependent on the type of zinc salts -the less soluble the zinc salt used, the higher its concentration should be in the agents.
  • the particle size of the salts is a criterion to be observed, so that the salts do not adhere to glassware or machine parts.
  • the insoluble zinc salts have a particle size below 1, 7 millimeters.
  • the insoluble zinc salt has an average particle size which is significantly below this value in order to further minimize the risk of insoluble residues, for example an average particle size of less than 250 ⁇ m. Again, this is even more true the less the zinc salt is soluble.
  • the glass corrosion inhibiting effectiveness increases with decreasing particle size.
  • the average particle size is preferably below 100 microns. For still less soluble salts, it may be even lower; For example, average particle sizes below 60 ⁇ m are preferred for the very poorly soluble zinc oxide.
  • Another preferred class of compounds are magnesium and / or zinc salt (s) of at least one monomeric and / or polymeric organic acid. These have the effect that, even with repeated use, the surfaces of glassware do not undergo corrosive changes, in particular no clouding, streaks or scratches, but also no iridescence of the glass surfaces.
  • magnesium and / or zinc salt (s) of monomeric and / or polymeric organic acids can be used, yet the magnesium and / or zinc salts of monomeric and / or polymeric organic acids from the groups of unbranched saturated or unsaturated monocarboxylic acids, the branched saturated or unsaturated monocarboxylic acids, the saturated and unsaturated dicarboxylic acids, the aromatic mono-, di- and tricarboxylic acids, the sugar acids, the hydroxy acids, the oxo acids, the amino acids and / or the polymeric carboxylic acids are preferred.
  • the spectrum of the inventively preferred zinc salts of organic acids ranges from salts which are difficult or insoluble in water, ie a solubility below 100 mg / l, preferably below 10 mg / l, in particular below 0.01 mg / l to those salts which have a solubility in water above 100 mg / l, preferably above 500 mg / l, more preferably above 1 g / l and especially above 5 g / l (all solubilities at 20 0 C water temperature).
  • the first group of zinc salts includes, for example, the zinc nitrate, the zinc oleate and the zinc stearate, and the group of soluble zinc salts includes, for example, zinc formate, zinc acetate, zinc lactate and zinc gluconate.
  • At least one zinc salt of an organic carboxylic acid more preferably a zinc salt from the group zinc stearate, zinc oleate, zinc gluconate, zinc acetate, zinc lactate and / or Zinkeitrat used.
  • Zinc ricinoleate, zinc abietate and zinc oxalate are also preferred.
  • the content of cleaning agents to zinc salt is preferably between 0.1 to 5 wt .-%, preferably between 0.2 to 4 wt .-% and in particular between 0.4 to 3 wt .-%, or the content of zinc in oxidized form (calculated as Zn 2+ ) is 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. %, in each case based on the total weight of the glaskorrosioninhibitorhaitigen agent.
  • Corrosion inhibitors serve to protect the items to be washed or the machine, with particular silver protectants being of particular importance in the field of automatic dishwashing. It is possible to use the known substances of the prior art. In general, silver protectants selected from the group of the triazoles, the benzotriazoles, the bisbenzotriazoles, the aminotriazoles, the alkylaminotriazoles and the transition metal salts or complexes can be used in particular. Particularly preferred to use are benzotriazole and / or alkylaminotriazole.
  • 3-amino-5-alkyl-1, 2,4-triazoles preferably used according to the invention which may be mentioned are: propyl, butyl, pentyl, heptyl, octyl, nonyl, decyl -, undecyl, - dodecyl, -sononyl, -Versatic-10-alkyl, -phenyl, -p-tolyl, - (4-tert-butylphenyl) -, - (4-methoxyphenyl) -, - (2-, 3-, 4-pyridyl) -, - (2-thienyl) -, - (5-methyl-2-furyl) -, - (5-oxo-2-pyrrolidinyl) -, -3 amino-1, 2,4-triazole.
  • the alkylamino-1,2,4-triazoles or their physiologically tolerated salts are present in a concentration of 0.001 to 10% by weight, preferably 0.0025 to 2% by weight, particularly preferably 0.01 to 0.04 wt .-% used.
  • Preferred acids for salt formation are hydrochloric acid, sulfuric acid, phosphoric acid, carbonic acid, sulphurous acid, organic carboxylic acids such as acetic, glycolic, citric, succinic acid.
  • cleaner formulations often contain active chlorine-containing agents which can markedly reduce the corrosion of the silver surface.
  • active chlorine-containing agents which can markedly reduce the corrosion of the silver surface.
  • oxygen- and nitrogen-containing organic redox-active compounds such as di- and trihydric phenols, for example hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucin, pyrogallol or derivatives of these classes of compounds used.
  • salt and complex inorganic compounds such as salts of the metals Mn, Ti, Zr, Hf, V, Co and Ce are often used.
  • transition metal salts which are selected from the group of the manganese and / or cobalt salts and / or complexes, particularly preferably the cobalt (ammin) complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) - Complexes, the chlorides of cobalt or manganese and manganese sulfate. Also, zinc compounds can be used to prevent corrosion on the items to be washed.
  • redox-active substances can be used. These substances are preferably inorganic redox-active substances from the group of manganese, titanium, zirconium, hafnium, vanadium, cobalt and cerium salts and / or complexes, wherein the metals preferably in one of the oxidation states II, III, IV, V or VI are present.
  • the metal salts or metal complexes used should be at least partially soluble in water.
  • the counterions suitable for salt formation include all conventional mono-, di-, or tri-negatively charged inorganic anions, e.g. Oxide, sulfate, nitrate, fluoride, but also organic anions such as e.g. Stearate.
  • Metal complexes in the context of the invention are compounds which consist of a central atom and one or more ligands and optionally additionally one or more of the above-mentioned.
  • Anions exist.
  • the central atom is one of the o.g. Metals in one of the above Oxidation states.
  • the ligands are neutral molecules or anions that are mono- or polydentate;
  • the term "ligand" within the meaning of the invention is e.g. in "Römpp Chemie Lexikon, Georg Thieme Verlag Stuttgart / New York, 9th edition, 1990, page 2507" explained in more detail.
  • the charge of the central atom and the charge of the ligand (s) do not add up to zero, either one or more of the above may be provided, depending on whether there is cationic or anionic charge excess.
  • Anions or one or more cations e.g. Sodium, potassium, ammonium ions, for charge balance.
  • Suitable complexing agents are e.g. Citrate, acetylacetonate or 1-hydroxyethane-1,1-diphosphonate.
  • metal salts and / or metal complexes are selected from the group MnSO 4 , Mn (II) citrate, Mn (II) stearate, Mn (II) acetylacetonate, Mn (II) - [1-hydroxyethane-1, 1- diphosphonate], V 2 O 5 , V 2 O 4 , VO 2 , TiOSO 4 , K 2 TiF 6 , K 2 ZrF 6 , CoSO 4 , Co (NO 3 ) 2 , Ce (NO 3 ) 3 , and mixtures thereof, such that the metal salts and / or metal complexes are selected from the group MnSO 4 , Mn (II) citrate, Mn (II) stearate, Mn (II)
  • metal salts or metal complexes are generally commercially available substances which can be used for the purpose of silver corrosion protection without prior purification in detergents or cleaners.
  • the mixture of pentavalent and tetravalent vanadium (V 2 O 5 , VO 2 , V 2 O 4 ) known from the SO 3 production (contact method) is suitable, as well as by diluting a Ti (SO 4 ) 2 solution of resulting titanyl sulfate, TiOSO 4 .
  • the inorganic redox-active substances are preferably coated, ie completely coated with a waterproof material which is readily soluble in the cleaning temperatures, in order to prevent their premature decomposition or oxidation during storage.
  • Preferred coating materials which are applied by known processes, such as Sandwik melt coating processes from the food industry, are paraffins, microwaxes, waxes of natural origin such as carnauba wax, candellila wax, beeswax, higher-melting alcohols such as hexadecanol, soaps or fatty acids.
  • the coating material which is solid at room temperature is applied in the molten state to the material to be coated, for example by spinning finely divided material to be coated in a continuous stream through a likewise continuously produced spray zone of the molten coating material.
  • the melting point must be selected so that the coating material dissolves easily during the silver treatment or melts quickly.
  • the melting point should ideally be in the range between 45 0 C and 65 ° C and preferably in the range 50 0 C to 60 ° C.
  • the metal salts and / or metal complexes mentioned are contained in cleaning agents, preferably in an amount of 0.05 to 6 wt .-%, preferably 0.2 to 2.5 wt .-%, each based on the total corrosion inhibitor-containing agent.
  • disintegration aids so-called tablet disintegrants
  • these compositions in order to shorten the disintegration times.
  • tablet disintegrants or disintegrants according to Römpp (9. Edition, Bd. 6, P. 4440) and Voigt "textbook of the pharmaceutical technology” (6th edition, 1987, pp. 182-184) understood auxiliary materials, which for the rapid disintegration of tablets into water or gastric juice and for the release of the Pharmaceuticals in resorbable form.
  • Disintegration aids are preferably used in amounts of from 0.5 to 10% by weight, preferably from 3 to 7% by weight and in particular from 4 to 6% by weight, based in each case on the total weight of the disintegration assistant-containing agent.
  • Preferred disintegrating agents used are cellulose-based disintegrating agents, so that preferred washing and cleaning agents comprise such a cellulose-based disintegrating agent in amounts of from 0.5 to 10% by weight, preferably from 3 to 7% by weight and in particular from 4 to 6% by weight. % contain.
  • Pure cellulose has the formal gross composition (C 6 H 10 Os) n and is formally a ⁇ -1,4-polyacetal of cellobiose, which in turn is composed of two molecules of glucose.
  • Suitable celluloses consist of about 500 to 5000 glucose units and therefore have average molecular weights of 50,000 to 500,000.
  • Cellulose-based disintegrating agents which can be used in the context of the present invention are also cellulose derivatives obtainable by polymer-analogous reactions of cellulose.
  • Such chemically modified celluloses include, for example, products of esterifications or etherifications in which hydroxy hydrogen atoms have been substituted.
  • Celluloses in which the hydroxy groups have been replaced by functional groups which are not bonded via an oxygen atom can also be used as cellulose derivatives.
  • the group of cellulose derivatives includes, for example, alkali metal celluloses, carboxymethylcellulose (CMC), cellulose esters and ethers, and aminocelluloses.
  • CMC carboxymethylcellulose
  • the cellulose derivatives mentioned are preferably not used alone as disintegrating agents based on cellulose, but used in admixture with cellulose.
  • the content of these mixtures of cellulose derivatives is preferably below 50% by weight, particularly preferably below 20% by weight, based on the cellulose-based disintegrating agent.
  • cellulose-based disintegrating agent which is free of cellulose derivatives.
  • the cellulose used as a disintegration aid is preferably not used in finely divided form, but converted into a coarser form, for example granulated or compacted, before it is added to the premixes to be tabletted.
  • the particle sizes of such disintegrating agents are usually above 200 .mu.m, preferably at least 90 wt .-% between 300 and 1600 .mu.m and in particular at least 90 wt .-% between 400 and 1200 microns.
  • the above and described in more detail in the documents cited coarser disintegration aids are preferred as disintegration aids and are commercially available, for example under the name of Arbocel ® TF-30-HG from Rettenmaier available in the present invention.
  • microcrystalline cellulose As a further disintegrating agent based on cellulose or as a component of this component microcrystalline cellulose can be used.
  • This microcrystalline cellulose is obtained by partial hydrolysis of celluloses under conditions which attack and completely dissolve only the amorphous regions (about 30% of the total cellulose mass) of the celluloses, leaving the crystalline regions (about 70%) intact. Subsequent deaggregation of the microfine celluloses produced by the hydrolysis yields the microcrystalline celluloses which have primary particle sizes of about 5 ⁇ m and, for example, can be compacted into granules having an average particle size of 200 ⁇ m.
  • Preferred disintegration aids preferably a disintegration aid based on cellulose, preferably in granular, cogranulated or compacted form, are present in the disintegrating agent-containing agents in amounts of from 0.5 to 10% by weight, preferably from 3 to 7% by weight and in particular from 4 to 6 wt .-%, each based on the total weight of the disintegrating agent-containing agent.
  • gas-evolving effervescent systems can furthermore be used as tablet disintegration auxiliaries.
  • the gas-evolving effervescent system may consist of a single substance that releases a gas upon contact with water.
  • these compounds mention should be made in particular of magnesium peroxide, which liberates oxygen on contact with water.
  • the gas-releasing effervescent system in turn consists of at least two constituents which react with one another to form gas. While a variety of systems are conceivable and executable here, which release, for example, nitrogen, oxygen or hydrogen, the bubble system used in detergents and cleaners can be selected both on the basis of economic and environmental considerations.
  • Preferred effervescent systems consist of alkali metal carbonate and / or bicarbonate and an acidifying agent which is suitable for liberating carbon dioxide from the alkali metal salts in aqueous solution.
  • the alkali metal carbonates or bicarbonates the sodium and potassium salts are clearly preferred over the other salts for reasons of cost.
  • the relevant pure alkali metal carbonates or bicarbonates do not have to be used; Rather, mixtures of different carbonates and bicarbonates may be preferred.
  • Acidifying agents that release carbon dioxide from the alkali salts in aqueous solution include, for example, boric acid and alkali metal hydrogen sulfates,
  • Alkali metal dihydrogen phosphates and other inorganic salts preference is given to using organic acidifying agents, the citric acid being a particularly preferred acidifying agent.
  • organic acidifying agents Tartaric acid, succinic acid, malonic acid, adipic acid, maleic acid, fumaric acid, oxalic acid and polyacrylic acid are again preferred from this group.
  • Organic sulfonic acids such as sulfamic acid are also usable.
  • a commercially available as an acidifier in the context of the present invention also preferably be used is Sokalan ® DCS (trademark of BASF), a mixture of succinic acid (max. 31 wt .-%), glutaric acid (max. 50 wt .-%) and adipic acid ( at most 33% by weight).
  • Acidifying agents in the effervescent system from the group of organic di-, tri- and oligocarboxylic acids or mixtures are preferred.
  • fragrance compounds for example the synthetic products of the ester type, ethers, aldehydes, ketones, alcohols and hydrocarbons, can be used in the context of the present invention.
  • Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethylmethylphenyl glycinate, allylcyclohexyl propionate, styrallyl propionate and benzyl salicylate.
  • the ethers include, for example, benzyl ethyl ether, to the aldehydes, for example, the linear alkanals having 8-18 carbon atoms, citral, citronellai, citronellyloxyacetaldehyde, cyclamen aldehyde, hydroxycitronellal, lilial and bourgeonal, to the ketones such as the ionone, oc-lsomethylionon and methyl cedrylketone , to the alcohols anethole, citronellol, eugenol, geraniol, linalool, Phenylethyl alcohol and terpineol, the hydrocarbons include mainly the terpenes such as limonene and pinene.
  • fragrance oils may also contain natural fragrance mixtures as are available from vegetable sources, eg pine, citrus, jasmine, patchouly, rose or ylang-ylang oil. Also suitable are muscatel, sage, chamomile, clove, lemon balm, mint, cinnamon, lime, juniper, vetiver, olibanum, galbanum and labdanum, and orange blossom, neroliol, orange peel and sandalwood.
  • fragrance To be perceptible, a fragrance must be volatile, whereby besides the nature of the functional groups and the structure of the chemical compound, the molecular weight also plays an important role plays. For example, most odorants have molecular weights up to about 200 daltons, while molecular weights of 300 daltons and above are more of an exception. Due to the different volatility of fragrances, the smell of a perfume or fragrance composed of several fragrances changes during evaporation, whereby the odor impressions in "top note”, “middle note” or “body note” ) and “base note” (end note or dry out).
  • the top note of a perfume does not consist solely of volatile compounds, while the base note is largely made up of less volatile, i. adherent fragrances.
  • more volatile fragrances can be bound to certain fixatives, preventing them from evaporating too quickly.
  • fixatives preventing them from evaporating too quickly.
  • Adhesion-resistant fragrances which can be used in the context of the present invention are, for example, the essential oils such as angelica root oil, aniseed oil, arnica blossom oil, basil oil, bay oil, bergamot oil, Champacablütenöl, Edel fir oil, Edeltannenzapfen oil, Elemiöl, eucalyptus oil, fennel oil, spruce needle oil, galbanum oil, geranium oil, ginger grass oil, Guaiac wood oil, gurdy balm oil, helichrysum oil, ho oil, ginger oil, iris oil, cajeput oil, calamus oil, chamomile oil, camphor oil, kanaga oil, cardamom oil, cassia oil, pine needle oil,
  • the essential oils such as angelica root oil, aniseed oil, arnica blossom oil, basil oil, bay oil, bergamot oil, Champacablütenöl, Edel fir oil, Edeltannenzapfen oil, Elemiöl,
  • fragrances can be used in the context of the present invention as adherent fragrances or fragrance mixtures, ie fragrances.
  • These compounds include the following compounds and mixtures thereof: ambrettolide, ⁇ -amylcinnamaldehyde, anethole, anisaldehyde, anisalcohol, anisole, methyl anthranilate, acetophenone, benzylacetone, benzaldehyde, ethyl benzoate, benzophenone, benzyl alcohol, benzyl acetate, benzyl benzoate, benzyl formate, benzyl valerate, borneol , Bornyl acetate, ⁇ -bromostyrene, n-decyl aldehyde, n-dodecyl aldehyde, eugenol, eugenol methyl ether, eucalyptol,
  • the more volatile fragrances include in particular the lower-boiling fragrances of natural or synthetic origin, which can be used alone or in mixtures.
  • fragrances examples include alkyl isothiocyanates (alkyl mustard oils), butanedione, limonene, linalool, linayl acetate and propionate, menthol, menthone, methyl-n-heptenone, phellandrene, phenylacetaldehyde, terpinyl acetate, citral, citronellal.
  • the fragrances can be processed directly, but it can also be advantageous to apply the fragrances on carriers that provide a slower fragrance release for long-lasting fragrance.
  • carrier materials for example, cyclodextrins have been proven, the cyclodextrin-perfume complexes can be additionally coated with other excipients.
  • Preferred dyes the selection of which presents no difficulty to the skilled person, have a high storage stability and insensitivity to the other ingredients of the compositions and to light and no pronounced substantivity to the substrates to be treated with the dye-containing agents, such as textiles, glass, ceramics or plastic dishes, so as not to stain them.
  • the above-mentioned Basacid ® Green or the above-mentioned Sandolan Blue ® are typically chosen dye concentrations in the range of a few 10 -2 to 10 -3 wt .-%.
  • the appropriate concentration of the colorant is in washing or cleaning agents, however, typically a few 10 "3 to 10" 4 wt .-% ,
  • Colorants are preferred which can be oxidatively destroyed in the washing process and mixtures thereof with suitable blue dyes, so-called blue toners. It has proved to be advantageous to use colorants which are soluble in water or at room temperature in liquid organic substances. Suitable examples are anionic colorants, for example anionic nitrosofarbstoffe.
  • One possible dye is, for example, naphthol green (Color Index (CI) Part 1: Acid Green 1; Part 2: 10020)., That is as a commercial product, for example as Basacid ® Green 970 from BASF, Ludwigshafen available, as well as mixtures thereof with suitable blue dyes.
  • Pigmosol come ® Blue 6900 (CI 74160), Pigmosol ® Green 8730 (CI 74260), Basonyl ® Red 545 FL (CI 45170), Sandolan® ® rhodamine EB400 (CI 45100), Basacid® ® Yellow 094 (CI 47005) Sicovit ® Patentblau 85 e 131 (CI 42051), Acid Blue 183 (CAS 12217-22-0, Cl Acidblue 183), pigment Blue 15 (Cl 74160), Supranol Blue ® GLW (CAS 12219-32-8, Cl Acidblue 221 )), Nylosan Yellow ® N-7GL SGR (CAS 61814-57-1, Cl Acidyellow 218) and / or Sandolan Blue ® (Cl Acid Blue 182, CAS 12219-26-0) is used.
  • the detergency enhancers of the combination products of the invention preferably contain builders and / or bleaches, with detergency enhancers having a builder and / or bleach content above 10 wt% being particularly preferred.
  • Particularly preferred detergency booster continue to contain in addition to further customary constituents of automatic cleaning agents, enzymes, bleach activators / bleach catalysts and / or surfactants, preferably nonionic surfactants.
  • the following table gives an overview of some particularly preferred formulations for detergency booster according to the invention. The stated parts by weight in% by weight are based on the total weight of the respective detergency booster.
  • washing power amplifier As a washing power amplifier are “acidic” as well as “alkaline” formulations.
  • combination products in which a 1% strength by weight solution of the detergency booster in distilled water at 20 ° C. has a pH above 10, preferably above 11.
  • Such combination products contain as builders preferably carbonates and / or phosphates and / or silicates or alkali carriers, preferably alkali carriers from the group of metal hydroxides, preferably sodium or potassium hydroxide.
  • Combination products containing these "alkaline" detergency booster are distinguished over conventional cleaners in particular by an improved cleaning performance of stubborn dirt such as tea or starch soiling and baked-on soils such as fatty encrustations, baked minced meat or baked cheese.
  • “acidic” formulations can also be used. Combination products in which a 1% strength by weight solution of the detergency booster in distilled water at 20 ° C. has a pH below 6, preferably below 4, are therefore preferred.
  • These "acidic" formulations contain as acid source preferably organic acids, in particular organic mono-, di- or polycarboxylic acids and / or polymeric organic acids a content of citric acid above 10 wt .-%, preferably above 20 wt .-%, preferably above 30 wt .-% and in particular above 40 wt.%.
  • the sum of the weight fractions of phosphate and the weight fractions of carbonate and the percentages by weight of percarbonate is between 40 and 95% by weight, preferably between 50 and 95% by weight, more preferably between 60 and 95% by weight and in particular between 70 and 95% by weight.
  • Preferred detergency boosters have a surfactant content below 10% by weight, preferably below 6% by weight, preferably below 4% by weight and in particular below 2% by weight.

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Abstract

La présente invention concerne des produits combinés destinés à des lave-vaisselle comprenant: a) un compartiment qui contient un amplificateur de force de lavage; b) un autre compartiment qui contient un agent de nettoyage principal; et c) une notice d'utilisation qui indique à l'utilisateur la manière dont il doit utiliser l'amplificateur de force de lavage au cours de la phase de prélavage, et l'agent de nettoyage principal au cours de la phase de lavage principale d'un processus de lavage au lave-vaisselle. Ces produits combinés se caractérisent par une puissance de nettoyage améliorée pour une consommation d'eau et d'énergie limitée au cours du processus de lavage au lave-vaisselle.
PCT/EP2005/011064 2004-10-22 2005-10-14 Unite de dosage d'agent de lavage ou de nettoyage WO2006045450A1 (fr)

Applications Claiming Priority (4)

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DE102004051560.3 2004-10-22
DE102004051560A DE102004051560A1 (de) 2004-10-22 2004-10-22 Wasch- oder Reinigungsmitteldosiereinheit
DE102004055075.1 2004-11-15
DE200410055075 DE102004055075A1 (de) 2004-10-22 2004-11-15 Wasch- oder Reinigungsmitteldosiereinheit

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0593952A1 (fr) * 1992-10-17 1994-04-27 DISPO-Kommerz AG Produit pour la libération d'agents de traitement dans le liquide laveur d'un lave-linge ou d'un lave-vaisselle automatique
DE19845602A1 (de) * 1998-10-05 2000-04-06 Henkel Kgaa Spülmittel-Tab-Packung für Geschirrspülmaschinen
EP1026230A1 (fr) * 1999-02-05 2000-08-09 Unilever Plc Kit de nettoyage pour la vaisselle
DE10035781A1 (de) * 1999-12-13 2001-07-12 Henkel Kgaa Waschmittel-, Spülmittel- oder Reinigungsmittel-Portionen mit kontrollierter Wirkstoff-Freisetzung
WO2004081161A1 (fr) * 2003-03-11 2004-09-23 Reckitt Benckiser N.V. Emballage contenant une composition detergente

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Publication number Priority date Publication date Assignee Title
GB8605734D0 (en) * 1986-03-07 1986-04-16 Unilever Plc Dispensing treatment agents
PL362605A1 (en) * 2000-11-27 2004-11-02 The Procter & Gamble Company Dishwashing method
GB2374581B (en) * 2001-04-20 2004-01-28 Reckitt Benckiser Water soluble containers
GB2374580B (en) * 2001-04-20 2003-07-16 Reckitt Benckiser Water-soluble containers
WO2003042347A1 (fr) * 2001-11-14 2003-05-22 The Procter & Gamble Company Composition pour lave-vaisselle automatique sous forme de dose unitaire comprenant un polymere anti-tartre
MXPA05005147A (es) * 2002-11-14 2005-07-22 Procter & Gamble Composicion de detergente para lavado de loza en lavavajillas automatica que comprende sal activa encapsulada para el cuidado de la cristaleria.

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0593952A1 (fr) * 1992-10-17 1994-04-27 DISPO-Kommerz AG Produit pour la libération d'agents de traitement dans le liquide laveur d'un lave-linge ou d'un lave-vaisselle automatique
DE19845602A1 (de) * 1998-10-05 2000-04-06 Henkel Kgaa Spülmittel-Tab-Packung für Geschirrspülmaschinen
EP1026230A1 (fr) * 1999-02-05 2000-08-09 Unilever Plc Kit de nettoyage pour la vaisselle
DE10035781A1 (de) * 1999-12-13 2001-07-12 Henkel Kgaa Waschmittel-, Spülmittel- oder Reinigungsmittel-Portionen mit kontrollierter Wirkstoff-Freisetzung
WO2004081161A1 (fr) * 2003-03-11 2004-09-23 Reckitt Benckiser N.V. Emballage contenant une composition detergente

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