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EP1412469A1 - Agent nettoyant pulverisable renfermant un composant apolaire sous forme de gouttelettes - Google Patents

Agent nettoyant pulverisable renfermant un composant apolaire sous forme de gouttelettes

Info

Publication number
EP1412469A1
EP1412469A1 EP02762381A EP02762381A EP1412469A1 EP 1412469 A1 EP1412469 A1 EP 1412469A1 EP 02762381 A EP02762381 A EP 02762381A EP 02762381 A EP02762381 A EP 02762381A EP 1412469 A1 EP1412469 A1 EP 1412469A1
Authority
EP
European Patent Office
Prior art keywords
agent according
phase
agent
aqueous phase
cleaning
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP02762381A
Other languages
German (de)
English (en)
Inventor
Bernhard Guckenbiehl
Michael Dreja
Erik BRÜCKNER
Marion Erbe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP1412469A1 publication Critical patent/EP1412469A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0017—Multi-phase liquid 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/1266—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in liquid 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions

Definitions

  • the invention relates to a multi-phase cleaner in which a droplet-shaped apolar component is incorporated so that a homogeneous distribution of the ingredients is ensured during use, preferably by spraying.
  • Sprayable cleaners are usually liquid or gel-like. Usually water, occasionally another polar solvent, forms the basis of the formulation.
  • the incorporation of non-polar additives therefore poses a problem for the person skilled in the art, particularly with a low surfactant content, the homogeneous distribution in the system is not always guaranteed.
  • a low surfactant content is desirable since high amounts of surfactant are not required in ready-to-use, that is to say undiluted, agents and can leave streaks when used as cleaning agents, and they also cause higher production costs.
  • a corresponding product must be available in a visually appealing form that is easy to handle by the consumer.
  • the incorporation of the hydrophobic phase as droplets and / or particles and / or bubbles is desirable.
  • these droplets or particles can float or sediment due to the difference in density, and on the other hand they can coagulate into a uniform phase.
  • Products are known from the prior art (e.g. WO 99/47635) and from the market, which the consumer has to shake before use in order to obtain a temporary emulsion. It must be ensured that a sufficient amount of active ingredient is applied to the surface to be cleaned even after very short or weak shaking. This makes handling difficult, especially with sprayable cleaners. It is therefore desirable to obtain a cleaner, in particular a sprayable cleaner, which keeps such droplets or particles in suspension due to its internal structure.
  • the application WO 96/37594 presents a multi-phase personal cleanser in which two oily components of different interfacial tension are dispersed.
  • the oil droplets have a maximum diameter of 30 ⁇ m and are kept stable there by the addition of clays and gums to the aqueous phase.
  • the use of such an agent for cleaning hard surfaces is just as little described as the possibility of spraying the agent.
  • Japanese publication JP 11 246348 A2 describes a multi-phase agent for cleaning the facial skin and for removing makeup.
  • An aqueous, surfactant-containing system is emulsified with an oil, so that the two phases originally present can no longer be distinguished by the consumer. Neither the cleaning of hard surfaces nor the spraying of the agent is described here.
  • European patent EP 490 749 B1 finally describes an agent in which an oil phase in the form of microspheres is present in an aqueous, surfactant-containing phase.
  • the microspheres sink to the bottom; by shaking, they are temporarily suspended in the aqueous phase.
  • the oil phase consists largely of dialkyl phthalates. Again, it is a cosmetic product that is neither intended for cleaning hard surfaces nor for spraying.
  • the object of the present invention is therefore to provide a preferably sprayable multiphase cleaner which combines the advantages of a cleaner with hydrophobic components and is thereby obtained in an optically appealing form which is easier for the consumer to handle, and which can be used directly, so that the disadvantages described are not occur more.
  • the aqueous phase of a multiphase cleaner for example by adding a thickener, can be given an internal structure through which a gaseous, solid or liquid phase in the form of bubbles and / or particles and / or droplets in suspension can be held.
  • a gaseous, solid or liquid phase in the form of bubbles and / or particles and / or droplets in suspension can be held.
  • the invention accordingly consists of a preferably sprayable, multi-phase cleaner which keeps a discontinuous gaseous and / or a discontinuous solid and / or a discontinuous liquid hydrophobic phase in suspension due to the internal structure of the continuous aqueous phase.
  • a further subject of the invention is a product which contains an agent according to the invention and a spray dispenser.
  • a third subject of the invention is the use of an agent according to the invention for cleaning hard surfaces, in particular glass, and as a pretreatment and cleaning agent for textiles.
  • a fourth subject of the invention is a method for cleaning and / or maintaining hard surfaces, in which the agent according to the invention, preferably by spraying, is applied to the surface to be cleaned and / or cared for and is wiped over the surface with an absorbent soft object to develop the cleaning effect.
  • a fifth subject of the invention is a process for cleaning and / or maintaining textile surfaces and for pretreating textiles, in which the agent according to the invention is applied, preferably by spraying, to the surface to be cleaned and, if appropriate after a contact time, by washing, suctioning or dabbing or wiping with a damp cloth or sponge.
  • the sixth object of the invention is a process for the preparation of the agent according to the invention, in which an outer aqueous phase with an inner structure is first produced, then an inner oil-containing phase is produced and this is then dispersed in the aqueous phase.
  • the aqueous phase preferably contains one or more thickeners to produce an internal structure.
  • Suitable thickeners are, for example, organic natural thickeners (agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, polyoses, guar flour, locust bean gum, starch, dextrins, gelatin, casein), organic modified natural substances (carboxymethyl cellulose and other cellulose ethers , Hydroxyethyl and propyl cellulose and the like, core meal ether), organic fully synthetic thickeners (polyacrylic and polymethacrylic compounds, vinyl polymers, polycarboxylic acids, polyethers, polyimines, polyamides) and inorganic thickeners (polysilicic acids, clay minerals such as montmorillonites, zeolites, silicas).
  • organic natural thickeners agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins,
  • the polyacrylic and polymethacrylic compounds include, for example, the high molecular weight homopolymers of acrylic acid crosslinked with a polyalkenyl polyether, in particular an allyl ether of sucrose, pentaerythritol or propylene (/ ⁇ / C / name according to the International Dictionary of Cosmetic Ingredients from The Cosmetic, Toiletry, and Fragrance Association (CTFA): Carbomer), also known as carboxyvinyl polymers be net.
  • CTFA Cosmetic, Toiletry, and Fragrance Association
  • Such polyacrylic acids are available, inter alia, from 3V Sigma under the trade name PolygeP, for example PolygeP DA, and from BFGoodrich under the trade name CarbopoP, for example CarbopoP 940 (molecular weight approx.
  • acrylic acid copolymers are also included: (i) Copolymers of two or more monomers from the group consisting of acrylic acid, methacrylic acid and their simple esters (/ ⁇ / C / acrylates copolymer), which are preferably formed with C 1-4 alkanols which include, for example, the copolymers of methacrylic acid, butyl acrylate and methyl methacrylate (C / AS name according to Chemical Abstracts Service: 25035-69-2) or of butyl acrylate and methyl methacrylate (CAS 25852-37-3) and which are available from Rohm & Haas are available under the trade names Aculyn ® and AcusoP, for example the anionic non-associative polymers Aculyn ® 22, Aculyn ® 28, Aculyn
  • Further thickeners are the polysaccharides and heteropolysaccharides, in particular the polysaccharide gums, for example gum arabic, agar, alginates, carragenes and their salts, guar, guarane, tragacanth, gellan, ramsan, dextran or xanthan and their derivatives, e.g. propoxylated guar, and their mixtures.
  • Other polysaccharide thickeners such as starches or cellulose derivatives, can alternatively, but preferably in addition to a polysaccharide rubber, for example starches of various origins and starch derivatives, e.g.
  • Layered silicates can also be used as thickeners. These include, for example, the magnesium or available under the trade name Laponite ® Sodium-magnesium layered silicates from Solvay Alkali, in particular Laponite ® RD or Laponite ® RDS, and magnesium silicates from Süd-Chemie, especially OptigeP SH.
  • layered silicates and / or water-soluble polymers are used as thickeners.
  • a combination of polymer and layered silicate is particularly advantageous, with an electrolyte possibly also being added.
  • Preferably are employed as polymers AcusoP 823, Aculyn ® 22, Aculyn ® 28 or PolygeP DA.
  • the concentration of the various thickeners in the aqueous phase is in each case 0.001 to 10%, preferably 0.1 to 5%, based on the aqueous phase.
  • the internal structure of the aqueous phase can also be produced in a different way than by adding polymeric thickeners.
  • liquid-crystalline structures or rod micelles can also stabilize the hydrophobic phase in an analogous manner.
  • these structures can only form at elevated surfactant concentrations, while the use of polymeric thickeners makes it possible to provide effective agents with low surfactant concentrations.
  • the oil phase contains a thickening agent to prevent shearing and thus irreversible destruction of the oil droplets when shaken or by moderate pumping.
  • Preferred polymeric or inorganic thickeners which can be used individually or together are silicas such as the Aerosile ® provided by Degussa, for example AerosiP R 972, organically modified layered silicates such as the organically modified montmorillonite Bentone ® 34 supplied by Rheox or oil-soluble polymers such as the styrene-ethylene / isoprene copolymer Kraton G® 1701-E from Shell.
  • the concentration of the various thickeners for the lipophilic phase is in each case 0.001 to 1%, preferably 0.005 to 0.1%, based on the total agent, or 0.01 to 20%, preferably 0.5 to 10%, based on the hydrophobic Phase.
  • the diameter of the dispersed oil droplets is 0.01 to 10 mm, preferably 0.1 to 4 mm.
  • the density difference between the oil and water phase is chosen to be as small as possible and the interfacial tension between these phases, on the other hand, is as large as possible. The latter is achieved through the low proportion of surfactants in the cleaner.
  • the interfacial tension between the oil and water phases is 0.002 to 100 mN / m, preferably 10 to 80 mN / m.
  • the agents according to the invention can contain anionic, nonionic, amphoteric or cationic surfactants or surfactant mixtures from one, several or all of these classes of surfactants, both in the aqueous and in the hydrophobic phase, as the surfactant component.
  • the compositions contain surfactants in amounts, based on the composition, of 0.001 to 20% by weight, preferably 0.1 to 10% by weight, particularly preferably 0.1 to 5% by weight.
  • Suitable anionic surfactants are the preferred C 8 -C 18 alkyl sulfates, C 8 -C 18 alkyl ether sulfates and / or C 8 -C 18 alkyl benzene sulfonates, but also C 8 -C 18 alkane sulfonates, C 8 -C 18 - ⁇ -olefin - sulfonates.sulfonated C 8 -C 18 fatty acids, in particular dodecylbenzenesulfonate, C 8 -C 22 carboxylic acid amide ether sulfates, sulfonic succinic acid mono- and di-CrC ⁇ 2 alkyl esters, C 8 -C 18 alkyl polyglycol ether carboxylates, C 8 -C ⁇ 8 - N-acyl taurides, C 8 -C 18 N sarcosinates and C 8 -C 18 alkyl isethionates or mixtures thereof.
  • compositions contain anionic surfactants in amounts, based on the composition, of 0 to 10% by weight.
  • Suitable nonionic surfactants are, for example, C 8 -C 18 alkyl alcohol polyglycol ethers, alkyl polyglycosides and nitrogenous surfactants or mixtures thereof, in particular the first two.
  • the compositions contain nonionic surfactants in amounts, based on the composition, of 0 to 10% by weight.
  • C 8 -C 8 -alkyl alcohol polypropylene glycol / polyethylene glycol ethers are preferred known nonionic surfactants. They can be described by the formula I, RO- (CH 2 CH (CH 3 ) O) p (CH 2 CH 2 O) e -H, in the for a linear or variable branched, aliphatic alkyl and / or alkenyl radical having 8 to 18 carbon atoms.p is 0 or numbers from 1 to 3 and e is numbers from 1 to 20.
  • the C 8 -C 18 alkyl alcohol polyglycol ethers of the formula I can be obtained by the addition of propylene oxide and / or ethylene oxide to alkyl alcohols, preferably to fatty alcohols.
  • Typical examples are polyglycol ethers of the formula I in which stands for an alkyl radical with 8 to 18 carbon atoms, p for 0 to 2 and e for numbers from 2 to 7.
  • End-capped C 8 -C 8 alkyl alcohol polyglycol ethers can also be used, ie compounds in which the free OH group in the formula I is etherified.
  • the end-capped C 8 -C 18 alkyl alcohol polyglycol ethers can be obtained by the relevant methods of preparative organic chemistry.
  • C 8 -C 18 -Alkyl alcohol polyglycol ethers are preferably reacted in the presence of bases with alkyl halides, in particular butyl or benzyl chloride.
  • Typical examples are mixed ethers of the formula I in which R is a technical fatty alcohol radical, preferably C 12 / ⁇ 4 -Kokos- alkyl, p is 0 and e is 5 to 10 are provided, which are closed with a butyl group.
  • Preferred nonionic surfactants are furthermore alkyl polyglycosides (APG) of the formula II, R "O [G] x , in which R" for a linear or branched, saturated or unsaturated alkyl radical having 8 to 22 carbon atoms, [G] for a glycosidically linked sugar radical and x stands for a number from 1 to 10.
  • APG are non-ionic surfactants and are known substances that can be obtained using the relevant methods of preparative organic chemistry.
  • the index number x in the general formula II indicates the degree of oligomerization (DP degree), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10.
  • Alkyl glycosides with an average degree of oligomerization x of 1.1 to 3.0 are preferably used. From an application point of view, preference is given to those alkyl glycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.6.
  • Xylose, but especially glucose, is preferably used as the glycosidic sugar.
  • the alkyl or alkenyl radical R "(formula II) can be derived from primary alcohols having 8 to 18, preferably 8 to 14, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol and their technical mixtures, as described, for example, in In the course of the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from ROELEN's oxosynthesis.
  • the alkyl or alkenyl radical R " is derived from lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol or oleyl alcohol.
  • Nitrogen-containing surfactants may be included as further nonionic surfactants, e.g. Fatty acid polyhydroxyamides, for example glucamides, and ethoxylates of alkylamines, vicinal diols and / or carboxamides which have alkyl groups with 10 to 22 C atoms, preferably 12 to 18 C atoms.
  • the degree of ethoxylation of these compounds is generally between 1 and 20, preferably between 3 and 10.
  • Ethanolamide derivatives of alkanoic acids having 8 to 22 C atoms, preferably 12 to 16 C atoms, are preferred.
  • the particularly suitable compounds include the lauric acid, myristic acid and palmitic acid monoethanolamides.
  • Suitable amphoteric surfactants are, for example, betaines of the formula (R '") (R lv ) (R v ) N + CH 2 COO " , in which R ⁇ i is an alkyl radical with 8 to 25, preferably 10 to 21, optionally interrupted by heteroatoms or heteroatom groups Carbon atoms and R ' v and R v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyldimethylcarboxymethylbetaine and Cn-C -alkylamidopropyldimethylcarboxymethylbetaine.
  • the compositions contain amphoteric surfactants in amounts, based on the composition, of 0 to 10% by weight.
  • Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R vl ) (R vil ) (R vm ) (R ix ) N + X-, in which R vi to R ix for four identical or different types, in particular two long and two short-chain, alkyl radicals and X "represent an anion, in particular a halide ion, for example didecyldimethylammonium chloride, alkylbenzyldecodylammonium chloride and mixtures thereof.
  • the compositions contain cationic surfactants in amounts, based on the composition, of 0 to 10% by weight.
  • the agents according to the invention contain anionic surfactants, preferably C 8 -C 18 alkyl sulfates and / or C 8 -C 18 alkyl ether sulfates.
  • the hydrophobic phase dispersed in the aqueous phase is based on aliphatic petroleum hydrocarbons (isoparaffins), terpene hydrocarbons and / or silicone oils.
  • the gasoline hydrocarbons preferably have a boiling point range from 130 to 260 ° C, in particular from 140 to 220 ° C, particularly preferably from 150 to 200 ° C.
  • Suitable terpene hydrocarbons which also have a cleaning effect, are, for example, citrus oils such as the orange oil obtained from the peel of oranges, the orange terpenes contained therein, in particular limes, and also citronell oil or pine oil.
  • lipophilic substances can also be present, such as fragrances, surface care agents such as fats, waxes or halogenated hydrocarbons, or skin-care ingredients such as ether or ester oils or glycerides.
  • the dispersed hydrophobic phase can also consist exclusively of isoparaffins, terpene hydrocarbons and / or silicone oil.
  • the volume fraction of the dispersed lipophilic phase in the total cleaning agent is 0.05 to 50%, preferably 0.1 to 10%, particularly preferably 0.2 to 5%
  • the aqueous phase of the agents according to the invention can contain one or more electrolyte salts.
  • Suitable electrolyte salts are, for example, the alkali metal and alkaline earth metal halides, in particular chlorides, and sulfates and nitrates, in particular sodium and potassium chloride and sulfate, and also ammonium chloride and sulfate or mixtures thereof.
  • Such salts support the phase separation through the salt effect as strong electrolytes which increase the ionic strength.
  • Sodium chloride has proven to be particularly effective here.
  • the compositions contain electrolyte salts in amounts, based on the composition, of 0 to 20% by weight.
  • Both the aqueous and the oily phase, one or more alcohols as further ingredients, fragrance A .offe, preservatives, coloring agents and other excipients may be added.
  • ethanol, isopropanol and n-propanol are used as alcohols.
  • Ethanol is particularly preferred in the context of the invention.
  • Preferred embodiments contain 0.05 to 10%, particularly preferably 1 to 10% alcohol.
  • Preferred auxiliaries and additives are perfume and fragrances and dyes, since the perfume and fragrances generally also support the phase separation in addition to the fragrance effect, while the phases can be colored differently by adding dyes, which improves the visual perception, especially of the dispersed hydrophobic Phase easier, and so the handling of the agent is made even easier.
  • the agent can contain gas bubbles as an additional discontinuous phase, which release a fragrance when the agent is used.
  • Air bubbles can also be contained, which, like the perfume bubbles, can also contribute to improved aesthetics of the product.
  • the agents according to the invention can contain builders. Suitable builders are, for example, alkali metal gluconates, citrates, nitrilotriacetates, carbonates and bicarbonates, in particular sodium gluconate, citrate and nitrilotriacetate, and sodium and potassium carbonate and bicarbonate. This also includes the salts of glutaric acid, succinic acid, adipic acid, tartaric acid and benzene hexacarboxylic acid as well as phosphonates and phosphates.
  • the compositions contain builders in amounts, based on the composition, of 0 to 15% by weight.
  • the agents according to the invention can contain bleaching agents or systems consisting of bleaching agent and activator / catalyst.
  • the bleaching agent and activator can be present in two different phases, so that they only come together when the agent is used, which ensures a higher storage stability.
  • the bleaching agents which can be used here include the substances which are well known from the prior art for use in washing and cleaning agents, for example those based on hypochlorite or also on peroxide.
  • bleach activators known from the prior art can be used as bleach activators. These include multiply acylated alkylenediamines, in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular 1,3 , 4,6-tetraacetylglycoluril (TAGU), N-acylimides, especially N-nonanoylsuccinimide (NOSI), acylated phenol sulfonates, especially n-nonanoyl- or isononanoyloxybenzenesulfonate (n- or iso-NOBS), acylated hydroxycarboxylic acids, such as triethylcarboxylic acids, O-acetyl citrate (TEAC), carboxylic anhydrides and their derivative
  • Hydrophilically substituted acylacetals and acyllactams can also be used.
  • Preferred bleach activators are sodium 4- (octanoyloxy) benzenesulfonate, undecenoyloxybenzenesulfonate (UDOBS), sodium dodecanoyloxybenzenesulfonate (DOBS) and / or decanoyloxybenzoic acid (DOBA, OBC 10).
  • the formanidinium salts disclosed in German patent application 198 01 049 can also be mentioned as further suitable bleach activators.
  • a mixture of several bleach activators can also be used.
  • Bleach activators of this type are in the customary quantitative range from 0.01 to 20% by weight, preferably in amounts from 0.1 to 15% by weight, in particular 1% by weight to 10% by weight, based on the total agent. contain.
  • the agents according to the invention can contain peroxo compounds.
  • Preferred peroxy compounds are H 2 O 2 and supplying compounds in water H 2 O 2 as sodium perborate monohydrate, Natriumpercar- carbonate or equivalent percarbonate salts, persilicate, peroxypyrophosphates, persulfates such as monopersulfate, urea peroxyhydrate, citrate, organic peroxides and HO 2 -supplying peracidic salts or peracids, such as perbenzoates, peroxophthalates, diperoxyazelaic acid, phthaloiminoperacids or diperoxydodecanedioic acid.
  • H 2 O 2 is particularly preferably used.
  • the sulfonimines and / or bleach-enhancing transition metal salts or transition metal complexes known from the European patents EP-A-0 446 982 and EP-A-0 453 003 can also be present as so-called bleaching catalysts.
  • the transition metal compounds in question include, in particular, the manganese, iron, cobalt, ruthenium or molybdenum salen complexes known from German patent application DE-A-195 29 905 and those known from German patent application DE-A-196 20 267 N-analog compounds, the manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes known from German patent application DE-A-195 36 082, which are described in German patent application DE-A-196 05 688 wrote manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with nitrogen-containing tripod ligands, the cobalt, iron, copper known from German patent application DE-A-196 20411 - and ruthenium-amine complexes, the manganese, copper and cobalt complexes described in German patent application DE 44 16438, the cobalt complexes described in European patent application EP-A-0 272 030, which are
  • bleach activators and transition metal bleach catalysts are known, for example, from German patent application DE-A-196 13 103 and international patent application WO-A-95/27775.
  • Bleach-enhancing transition metal complexes in particular with the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, are used in customary amounts, preferably in an amount of up to 1% by weight, in particular 0.0025% by weight. % to 0.25% by weight and particularly preferably from 0.01% by weight to 0.1% by weight, in each case based on the total agent.
  • the agents according to the invention can contain abrasives.
  • Solid water-soluble and water-insoluble, preferably inorganic compounds and mixtures thereof can serve as the abrasive component. These include, for example, alkali carbonates, alkali bicarbonates and alkali sulfates, alkali borates, alkali phosphates, silicon dioxide, crystalline or amorphous alkali silicates and layered silicates, finely crystalline sodium aluminum silicates and calcium carbonate.
  • the advantage of water-soluble abrasive components is that the agent can be rinsed off practically without residue. A restriction with regard to the abrasives used only exists in the particle size of the abrasive, which must be allowed by the dosage from the spray dispenser or other storage container used.
  • the agents according to the invention can contain further auxiliaries and additives as are customary in such agents.
  • auxiliaries and additives include in particular polymers, soil release agents, solubilizers, hydrotropes (e.g. cumene sulfonate, octyl sulfate, butyl glucoside, butyl glycol), cleaning enhancers, pH regulators (e.g. citric acid, alkanolamines or sodium hydroxide), disinfectants, antistatic agents, Preservatives, enzymes (especially lipases, amylases), optical brighteners and opacifiers or skin protection agents, as described in EP-A-522 506.
  • the amount of such additives is usually not more than 12% by weight in the cleaning agent. The lower limit of use depends on the type of additive.
  • the amount of auxiliaries is preferably between 0.01 and 7% by weight, in particular 0.1 and 4% by weight.
  • the pH of the compositions according to the invention can be varied over a wide range, but a range from 1.5 to 13, in particular 2.3 to 12 is preferred. Within the scope of the present invention, the pH is below the pH of the compositions according to the invention - To understand the value of the aqueous phase.
  • the agents according to the invention can be formulated as acidic cleaning agents.
  • they can contain acids, preferably citric acid, amidosulfonic acid, lactic acid, salicylic acid, formic acid, hydrochloric acid.
  • Acidic cleaning agents according to the invention preferably have a pH of 1.5 to 6, particularly preferably 2.3 to 4.5.
  • the viscosity of the continuous aqueous phase is 500 to 80,000 mPas, that of the discontinuous hydrophobic phase 10 to 30,000 mPas (rotary rheometer, plate-plate, 25 ° C, 1 ⁇ rad / s).
  • the agent according to the invention is sprayable and can therefore be used in a spray dispenser.
  • Another object of the invention is accordingly a product containing an agent according to the invention and a spray dispenser.
  • the spray dispenser is preferably a manually activated spray dispenser, in particular selected from the group comprising aerosol spray dispensers, self-building spray dispensers, pump spray dispensers and trigger spray dispensers, in particular pump spray dispensers and trigger spray dispensers with a container made of transparent polyethylene or polyethylene terephthalate.
  • Spray dispensers are described in greater detail in WO 96/04940 (Procter & Gamble) and the US patents cited therein for spray dispensers, all of which are referenced in this regard and the contents of which are hereby incorporated into this application.
  • the agents according to the invention are preferably used as cleaning agents for hard surfaces in such a way that the agent, which may be temporarily converted into an emulsion by shaking, but preferably applied without shaking, is applied to the surface to be cleaned and / or cared for and immediately thereafter wipe these surfaces with an absorbent soft object, thereby cleaning and / or caring for them.
  • the agents are preferably applied with the aid of suitable spray devices, in particular a spray dispenser or a product according to the invention, in order to achieve a distribution which is as uniform as possible. Sponges or cloths, which can be rinsed out with water from time to time when treating larger areas, are particularly suitable for wiping.
  • An embodiment of the agent can also be used for manual dishwashing.
  • the agent is applied to the soiled dishes and, if necessary after a contact time of 10 to 30 minutes to remove stubborn incrustations, in hot water with a sponge, a brush, a cloth or other objects usually used for cleaning dishes, together with the Soiling removed again.
  • the agent can be added to the (hot) water which is to be used for washing, so that a detergent solution is formed in which the dishes can be cleaned in the customary manner.
  • the use of the agent according to the invention as a textile pretreatment agent and as an agent for removing stains on carpets, upholstery, etc. is preferably carried out in such a way that the agent is applied, preferably by spraying, to the piece of textile to be cleaned and after an exposure time which depends on the type and nature of the soiling and depends on the textile material to be cleaned and is usually between 10 and 60 minutes, removed by washing, dabbing or rubbing with a damp absorbent cloth or sponge or vacuuming with a suitable vacuum cleaner.
  • the agent can also be rubbed mechanically on the stain during the exposure time.
  • an embodiment of the agent according to the invention can also be used to support the cleaning action of commercially available detergents for washing textiles in washing machines and for cleaning and maintaining sensitive textiles in hand basins.
  • the agents according to the invention are produced by first producing an outer aqueous phase which has an inner structure, for example by adding thickeners. An inner hydrophobic phase is then generated. This is finally dispersed in the outer aqueous phase.
  • the agents according to the invention can also be produced in a continuous process.
  • the oil droplets were stained blue or in one case green and worked in stably over a period of several weeks and at fluctuating temperature intervals (10-40 ° C).
  • the droplet size of the discontinuous phase each had a size distribution between 0.05 and 2 mm.
  • Texapon ® NSO lauryl ether sulfate sodium salt (Cognis)
  • Acusol ® 823 acrylic polymer (Rohm & Haas)
  • Aculyn ® 28 acrylic polymer (ISP)
  • Polygel ® DA carboxyvinyl polymer (3V Sigma)
  • Optigel SH synthetic.
  • Dyes blue Sudan blue FF 4214, fat blue, sandoplast blue 2B, heliogen blue 1701, cosmenyl blue; green: cosmenyl green

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

Abstract

L'invention concerne des agents aqueux, sous forme de gels, multiphases, renfermant des tensio-actifs, contenant au moins une phase aqueuse (I) et une phase hydrophobe (II), non miscible avec cette phase aqueuse, la phase hydrophobe étant maintenue en suspension, sous forme de bulles et/ou de particules et/ou de gouttelettes, dans la phase aqueuse. Les agents précités sont utilisés, éventuellement sous forme d'un produit renfermant un véhiculeur de pulvérisation, pour le nettoyage de surfaces dures ou de surfaces textiles, en pulvérisant l'agent, sans l'agiter au préalable, sur la surface à nettoyer ou en l'appliquant d'une toute autre façon au moyen d'un réservoir. L'agent nettoyant selon l'invention est fabriqué en créant une structure interne dans une phase aqueuse extérieure et en dispersant dans celle-ci, la phase hydrophobe interne, après sa production, de telle façon que les bulles et/ou particules et/ou gouttelettes soient détectables, au moins en partie, à l'oeil nu.
EP02762381A 2001-07-31 2002-07-20 Agent nettoyant pulverisable renfermant un composant apolaire sous forme de gouttelettes Withdrawn EP1412469A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE2001137047 DE10137047A1 (de) 2001-07-31 2001-07-31 Versprühbarer Reiniger, enthaltend eine tröpfchenförmige apolare Komponente
DE10137047 2001-07-31
PCT/EP2002/008119 WO2003012023A1 (fr) 2001-07-31 2002-07-20 Agent nettoyant pulverisable renfermant un composant apolaire sous forme de gouttelettes

Publications (1)

Publication Number Publication Date
EP1412469A1 true EP1412469A1 (fr) 2004-04-28

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP02762381A Withdrawn EP1412469A1 (fr) 2001-07-31 2002-07-20 Agent nettoyant pulverisable renfermant un composant apolaire sous forme de gouttelettes

Country Status (3)

Country Link
EP (1) EP1412469A1 (fr)
DE (1) DE10137047A1 (fr)
WO (1) WO2003012023A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7448556B2 (en) 2002-08-16 2008-11-11 Henkel Kgaa Dispenser bottle for at least two active fluids
DE10343851A1 (de) * 2003-09-23 2005-04-14 Beiersdorf Ag Sprühbare kosmetische Formulierung
US20060090777A1 (en) * 2004-11-01 2006-05-04 Hecht Stacie E Multiphase cleaning compositions having ionic liquid phase
US7939485B2 (en) 2004-11-01 2011-05-10 The Procter & Gamble Company Benefit agent delivery system comprising ionic liquid
US7776810B2 (en) 2004-11-01 2010-08-17 The Procter & Gamble Company Compositions containing ionic liquid actives
US7737102B2 (en) 2004-11-01 2010-06-15 The Procter & Gamble Company Ionic liquids derived from functionalized anionic surfactants
US7786065B2 (en) 2005-02-18 2010-08-31 The Procter & Gamble Company Ionic liquids derived from peracid anions
WO2009100227A1 (fr) * 2008-02-05 2009-08-13 Amcol International Corporation Compositions de nettoyage résistantes à l’égouttement
CN116574568B (zh) * 2023-03-07 2025-08-26 榆林市金世源矿用油品有限公司 一种多功能玻璃水及其制备方法

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1303810A (fr) * 1969-05-02 1973-01-24
US4793942A (en) * 1987-01-08 1988-12-27 Ecolab Inc. Detersive systems with a dispersed aqueous-organic softening agent for hardness removal
ATE242313T1 (de) * 1998-03-16 2003-06-15 Henkel Kgaa Verwendung eines wässrigen mehrphasigen reinigungsmittels zur reinigung harter oferflächen
US6720300B1 (en) * 1998-10-26 2004-04-13 Reckitt Benckiser N.V. Liquid cleaning agent or detergent composition
DE19859778A1 (de) * 1998-12-23 2000-06-29 Henkel Kgaa Mehrphasiges Reinigungsmittel mit Naphthalinsulfonsäure-Formaldehyd-Kondensat

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO03012023A1 *

Also Published As

Publication number Publication date
WO2003012023A1 (fr) 2003-02-13
DE10137047A1 (de) 2003-02-27

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