EP2334776B1 - Detergent composition comprising mixture of chelants - Google Patents
Detergent composition comprising mixture of chelants Download PDFInfo
- Publication number
- EP2334776B1 EP2334776B1 EP10748205A EP10748205A EP2334776B1 EP 2334776 B1 EP2334776 B1 EP 2334776B1 EP 10748205 A EP10748205 A EP 10748205A EP 10748205 A EP10748205 A EP 10748205A EP 2334776 B1 EP2334776 B1 EP 2334776B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- liquid detergent
- detergent composition
- compact liquid
- chelants
- composition
- 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.)
- Not-in-force
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/33—Amino carboxylic acids
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3245—Aminoacids
Definitions
- the present invention relates to a compact liquid detergent used in laundry cleaning comprising a mixture of chelants.
- Chelants are often formulated in detergents because of the presence of metal ions, which can be detrimental to end performance. Many highly colored stains incorporate metals. Removal of the metal can often decolorize the stain and/or make it easier to remove by destabilizing its structure. Metal ions can also catalytically decompose bleach in a formulation leading to a significantly reduced performance. Especially transition metal radical ions e.g. Fe, Cu and Mn can accelerate bleach and peroxide decomposition during washing and bleaching. Water hardness ions e.g. Ca and Mg can also cause adverse interaction with surfactants used in washing formulations and lead to a reduction in the effective concentration available. Fatty acids can precipitate as calcium soaps resulting in the formation of soap scum.
- Chelants are widely used chemicals that control adverse effects of metal ions in detergent products by chelating the metal.
- the chelants are often organic compounds, which form multiple bonds with a single metal ion.
- Chelants can be introduced into the detergent in an acid form or in a salt form; normally the salt form increases the water-solubility of the chelant.
- sodium ions will interact with the fatty acids of the detergent composition resulting in the formation of solid soap. Therefore chelants need to be formulated into the composition containing as small amount of sodium ions as possible, nevertheless maintaining the solubility of the chelants.
- Another requirement for the chelants is their solubility. Selected chelants need to be soluble and stay soluble without the requirement of added water into the detergent composition. Additionally chelants need to be stable in solution during the storage.
- Phosphate containing chelants have been used widely because of phosphates capability to sequester alkaline earth metals.
- level of phosphate in detergents needs to be substantially reduced.
- detergent manufacturers are supply more phosphate free detergents. Therefore the detergent composition formulation needs to fulfill the requirements of regulatory requirements in different countries.
- the chelant When formulating the compact liquid detergent composition the chelant needs to be selected to fulfill the criteria to control the metal ions, be soluble in the detergent composition, be stable during the preparation and storage and fulfill the regulatory requirements.
- the Applicant has surprisingly found that by combining chelants diethylene triamine pentaacetate (DTPA), in a sodium salt form with S,S-ethylene diamine disuccinic acid (EDDS) in a 2-amminoethanol neutralized form or in sodium salt form, the overall quantity of chelants can be decreased while maintaining good solubility and high activity level. Additionally the quantity of undesired sodium ions brought into the compact liquid detergent composition is reduced and therefore formation of undesired sodium soap is reduced.
- the compact liquid detergent composition of the present invention also covers wider regulatory requirements and can be used as global formulation.
- Chelants are known for incorporation into cleaning compositions.
- WO2009/013534 (Innospec Limited) salt of ethylenediamine disuccinic acid (EDDS) is used to stabilize the hydrogen peroxide.
- WO2009/013539 (Innospec Limited) magnesium salt of ethylenediamine disuccinic acid (EDDS) is used in detergent composition in water-soluble, non-hydroscopic solid form.
- WO2009/013541 Innospec Limited
- HEDP 1-hydroxyethylidene-1,1-diphosphonic acid
- EDDS ethylenediamine disuccinic acid
- a compact liquid detergent composition comprising less than 25% water by weight of the composition and a mixture of chelants, wherein first chelant is selected from the group consisting of sodium salt of Ethylenediamine- N , N '-disuccinic acid, Ethylenediamine-N,N'-disuccinic acid neutralized by 2-aminoethanol and mixtures thereof and second chelant is sodium salt of diethylene triamine pentaacetate.
- the detergent product of the present invention is a compact liquid detergent suitable to be used in a water-soluble pouch, more preferably a multi-compartment water-soluble pouch or as a conventional liquid detergent conserved in containers.
- the water-soluble pouch where present, comprises a water-soluble film and at least a first, and optionally a second compartment.
- the first compartment comprises a first composition, comprising a mixture of chelants.
- the second compartment comprises a second composition.
- the pouch comprises a third compartment and a third composition.
- the optionally second and third compositions are preferably visibly distinct from each other and the first composition.
- the composition of the present invention is a compact liquid.
- 'liquid' it is meant to include liquid, paste, waxy or gel compositions.
- the liquid composition may comprise a solid. Solids may include powder or agglomerates, such as micro-capsules, beads, noodles or one or more pearlised balls or mixtures thereof. Such a solid element may provide a technical benefit, through the wash or as a pre-treat, delayed or sequential release component. Alternatively it may provide an aesthetic effect.
- 'compact' is meant to include liquid, paste, waxy or gel compositions which comprise less than 25% of water by the weight of the composition.
- the present composition is in the form of a water-soluble pouch, more preferably a multi-compartment pouch.
- the water-soluble pouch wherein present, comprises a water-soluble film and at least a first, and optionally a second compartment.
- the first compartment comprises a first composition, comprising the mixture of chelants.
- the second compartment comprises a second, preferably different composition.
- the chelants are used in the present invention to control metal ion content, to stabilize bleach in washing solution and during storage and increase the stain removal by abstracting metal ions from the stains.
- Chelants are molecules which form coordinate-covalent bonds with metal ions to form chelates.
- Chelates are coordination compounds in which a central metal atom bonds one or more atoms in at least one other molecule or ion called ligand such that at least one heterocyclic ring is formed with the metal ion as part of the each ring.
- Chelants are widely used in detergents, soaps, cleaning products and water treatment.
- Chelants are typically polyvalent molecules, usually aminocarboxylates having at least two binding site. The effectiveness of the chelants can be measured by measuring the binding constant with the various metals. Within limits, chelants are usually more effective at increasing wash solution pH, which prevents protonation of chelants.
- chelants diethylene triamine pentaacetate (DTPA) in sodium salt form with S,S- Ethylenediamine-N,N'-disuccinic acid (EDDS) in 2-aminoethanol (MEA) neutralized form or in a sodium salt form, creates a synenergy between the chelants, and quantity of chelants can be decreased while maintaining high activity level and desired solubility. This permits more flexibility in formulation. Additionally the quantity of undesired sodium ions brought into compact liquid detergent composition is reduced. Reduced level of chelants improves the solubility and stability of chelants and permits the use of mixture of chelants in compact liquid detergent compositions.
- the compact liquid detergent composition of the present invention also covers wider regulatory requirements because the chelants do not contain any phosphates.
- the chelants are preferably both in the fully neutralized form; however the acid form or partially neutralized forms of Ethylenediamine- N,N' -disuccinic acid are encompassed in the invention.
- the chelant mixture preferably comprises from 1 : 10 molar ratio of diethylene triamine pentaacetate and ethylenediamine-N,N' disuccinic acid or their salts to 10 : 1 molar ratio of diethylene triamine pentaacetate and ethylenediamine-N-N disuccinic acid or their salts.
- EDDS is an effective chelating agent of transitional metals and heavy metals. Transitional metals may cause problems in compositions containing bleaching agents as they can cause decomposition of peroxide species. This may cause reduced bleaching performance and creation of hydroxyl radicals which can cause fibre damage and reduce product stability.
- EDDS has two stereogenic centers and therefore has three possible stereo isomers.
- the mixture of the chelants in a present invention may include any of the stereoisomers. Thus it may be selected from [R,R]-EDDS, [R,S]-EDDS, [S,S]-EDDS and any combinations thereof.
- the EDDS is present in substantially the [S,S]-form. Preferably at least 50%, more preferably at least 70% of the EDDS is of the [S,S] configuration. [S,S] - EDDS form of EDDS is biodegradable and therefore most preferred stereoisomer.
- EDDS can be present in compact liquid detergent composition in sodium salt or MEA neutralied form, preferably in MEA neutralied form.
- DTPA is an effective chelating agent of transitional metals and heavy metals.
- DTPA is a polyamino carboxylic acid consisting of a diethylenetriamine backbone modified with five carboxymethyl groups.
- DTPA is used as its conjugate base, which has a high affinity for metal cations.
- DTPA can be present in a compact liquid detergent composition preferably DTPA in metal salt form. More preferably the DTPA is present in compact liquid detergent composition in the form of sodium salt comprising from 2 to 5 moles of sodium per mole of DTPA.
- the chelants are added to the composition preferably in liquid form and they preferably stay in liquid form during preparation, storage and usage.
- DTPA is water-soluble in 1:2 ratio with sodium
- EDDS is water-soluble in aminoethanol neurtalised form or in 1:2 ratio with sodium.
- the combination of chelants in the present invention comprises from ten moles of EDDS MEA neutralized form per one mole of DTPA sodium salt to one mole of EDDS MEA neutralized form per ten moles of DTPA sodium salt.
- composition of the present invention comprises mixture of chelants from 0.05% to 5% by weight of a composition, preferably from 0.1% to 4% by weight of the composition and most preferably from 0.5% to 2.0% by weight of the composition.
- compositions of the present invention may comprise one or more of the ingredients as discussed below.
- the solvent system in the present compact liquid detergent compositions can be a mixture of organic solvents.
- the present composition does not contain any added water. High water content may have an unwanted effect on the film properties. Additionally too high or too low water content may have negative impact on detergent composition i.e. by causing phase separation.
- the water in the composition origins from the raw materials.
- Preferred organic solvents include 1,2-propanediol, ethanol, glycerol, dipropylene glycol, methyl propane diol and mixtures thereof. Other lower alcohols, C 1 -C 4 alkanolamines such as monoethanolamine and triethanolamine, can also be used.
- Solvent systems can be absent, for example from anhydrous solid embodiments of the invention, but more typically are present at levels in the range of from 0.1% to 98%, preferably at least 1% to 50%, more usually from 5% to 25%.
- Water is typically present at levels in the range from 5% to 25%, preferably from 7% to 20% more preferably from 8% to 15% by the weight of the compact liquid detergent composition.
- composition of the present invention may comprise surfactants, which are used in present invention as detersive surfactant for soil suspension purposes.
- Surfactants utilized can be of the anionic, nonionic, zwitterionic, ampholytic or cationic type or can comprise compatible mixtures of these types. More preferably surfactants are selected from the group consisting of anionic, nonionic, cationic surfactants and mixtures thereof. Preferably the compositions are substantially free of betaine surfactants.
- Detergent surfactants useful herein are described in U.S. Patent 3,664,961, Norris, issued May 23, 1972 , U.S. Patent 3,919,678, Laughlin et al., issued December 30, 1975 , U.S. Patent 4,222,905, Cockrell, issued September 16, 1980 , and in U.S. Patent 4,239,659, Murphy, issued December 16, 1980 .
- Anionic and nonionic surfactants are preferred.
- Useful anionic surfactants can themselves be of several different types.
- water-soluble salts of the higher fatty acids i.e., "soaps"
- This includes alkali metal soaps such as the sodium, potassium, ammonium, and alkyl ammonium salts of higher fatty acids containing from 8 to 24 carbon atoms, and preferably from 12 to 18 carbon atoms.
- Soaps can be made by direct saponification of fats and oils or by the neutralization of free fatty acids.
- Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium or potassium tallow and coconut soap.
- non-soap anionic surfactants which are suitable for use herein include the water-soluble salts, preferably the alkali metal, and ammonium salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from 10 to 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
- alkyl is the alkyl portion of acyl groups.
- this group of synthetic surfactants are a) the sodium, potassium and ammonium alkyl sulfates, especially those obtained by sulfating the higher alcohols (C 8 -C 18 carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; b) the sodium, potassium and ammonium alkyl polyethoxylate sulfates, particularly those in which the alkyl group contains from 10 to 22, preferably from 12 to 18 carbon atoms, and wherein the polyethoxylate chain contains from 1 to 15, preferably 1 to 6 ethoxylate moieties; and c) the sodium and potassium alkylbenzene sulfonates in which the alkyl group contains from 9 to 15 carbon atoms, in straight chain or branched chain configuration, e.g., those of the type described in U.S.
- Patents 2,220,099 and 2,477,383 Especially valuable are linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from 11 to 13, abbreviated as C 11 -C 13 LAS.
- Preferred nonionic surfactants are those of the formula R 1 (OC 2 H 4 ) n OH, wherein R 1 is a C 10 -C 16 alkyl group or a C 8 -C 12 alkyl phenyl group, and n is from 3 to 80.
- Particularly preferred are condensation products of C 12 -C 15 alcohols with from 5 to 20 moles of ethylene oxide per mole of alcohol, e.g., C 12 -C 13 alcohol condensed with 6.5 moles of ethylene oxide per mole of alcohol.
- composition of the present invention comprises from 1% to 80% surfactant by weight of a composition.
- Surfactant is a component of the first composition.
- Preferably said first composition comprises from 5% to 50% surfactant by weight of composition.
- the second and third compositions, where present, may comprise surfactant at levels of from 0.1 to 99.9%.
- the composition comprises preferably from 5% to 30% of LAS by weight of the compact liquid detergent composition, more preferably from 7% to 25% of LAS by weight of the compact liquid detergent composition.
- composition of the present invention may optionally comprise polymers.
- Polymers suitable for the present invention can boost the efficacy of the surfactant, thus they are called surfactant boosting polymers.
- the most common purpose of a surfactant is to emulsify or disperse one liquid phase into another - usually the oil phase into water. When two immiscible liquids are in contact, a boundary forms between them. Increasing the interface area, results in the dispersion of one phase into another as small droplets. The lower the interfacial tension is the more one phase is emulsified into other. Therefore a low interfacial tension is correlated with cleaning efficiency in cleaning and laundering.
- surfactant boosting polymer is meant polymers capable of decreasing the time to reach the interfacial tension equilibrium of the surfactant.
- surfactant boosting polymers aid the collapse of micelles on fats.
- a key feature of the surfactant boosting polymer is their amphiphilicity. They have a balanced ratio of hydrophobic and hydrophilic structural elements. Hence they are firstly hydrophobic enough to absorb a hydrophobic soil and to remove it with the surfactants from a surface. Secondly it is hydrophilic enough to keep the detached hydrophobic soil in the washing and cleaning liquor and prevent it from redepositing onto the surface.
- polyethylene glycol polyvinyl acetate (PEG-PVAc) polymer For example in the polyethylene glycol polyvinyl acetate (PEG-PVAc) polymer; hydrophobic PVAc part of the PEG-PVAc polymer ensures interaction with surfactant and hydrophobic grease stains, while the hydrophilic polyethylene glycol PEG part of the PEG-PVAc polymer keeps polymer-surfactant structures dispersed in water.
- PEG-PVAc polyethylene glycol polyvinyl acetate
- amphiphilic surfactant boosting polymers in a present invention are preferably based on water-soluble polyalkylene oxides as the hydrophilic back bone and hydrophobic side chains formed by polymerization of a vinyl ester component.
- Said polymers preferably have an average of one or less graft site per 50 alkylene oxide units and mean molar masses M w from 3000 to 100,000.
- surfactant boosting polymers for the present invention are known under the trade reference Sokalan PG101 (PEG-PVAc), Sokalan and Sokalan HP22 sold by BASF Aktiengesellschaft, Ludwigshafen, Germany.
- Surfactant boosting polymers useful herein are described in WO 2007/138053 (BASF Aktiengesellesschaft), WO/2007/138054 (Procter & Gamble Company).
- the compact liquid detergent composition of the present application comprises from 0.1% to 10% surfactant boosting polymer by weight of the compact liquid detergent composition, preferably from 3% to 8% surfactant boosting polymer by weight of the compact liquid detergent composition and more preferably about 4% surfactant boosting polymer by weight of the compact liquid detergent composition.
- the compact liquid detergent composition may comprise an opacifier.
- An opacifier according to the present invention is a solid, inert compound which does not dissolve in the composition and refracts, scatters or absorbs most light wavelengths.
- the opacifier is preferably selected from the group consisting of styrene/acrylate latexes, titanium dioxide, tin dioxide, any forms of modified TiO 2 , for example carbon modified TiO 2 or metallic doped (e.g. Platinum, Rhodium) TiO 2 or stannic oxide, bismuth oxychloride or bismuth oxychloride coated TiO 2 /Mica, silica coated TiO 2 or metal oxide coated and mixtures thereof.
- Particularly preferred styrene/acrylate latexes are those available from the Rohm & Haas Company sold under the trademark Acusol.
- the latexes are characterized by pH of about 2 to about 3, having approximately 40% solids in water, with particle size of about 0.1 to about 0.5 micron.
- Acusol.RTM. polymers include Acusol.RTM. OP301 (styrene/acrylate) polymer, Acusol.RTM. OP302, (Styrene/Acrylate/Divinylbenzene Copolymer), Acusol.RTM. OP303 (Styrene/Acrylamide Copolymer), Acusol.RTM.
- OP305 (Styrene/PEG-10 Maleate/Nonoxynol-10 Maleate/Acrylate Copolymer) and (Styrene/Acrylate/PEG-10 Dimaleate Copolymer) and mixtures thereof.
- Preferred species have molecular weight of from 1000 to 1 000 000, more preferably from 2000 to 500 000, most preferably from 5000 to 20 000.
- the opacifier is preferably present in sufficient amount to leave the composition, in which it is incorporated, white.
- the opacifier is an inorganic opacifier (e.g. TriO 2 , or modifications thereof) the opacifier is preferably present at a level of from 0.001% to 1%, more preferably from 0.01% to 0.5%, most preferably from 0.05% to 0.15% by weight of the compact liquid detergent composition.
- the opacifier is an organic opacifier (e.g. styrene/acrylate latexes)
- the opacifier is preferably present at a level of from 0.001% to 2.5%, more preferably from 1% to 2.2%, most preferably from 1.4% to 1.8% by weight of the compact liquid detergent composition.
- the compact liquid detergent composition may comprise an antioxidant.
- the second and third compositions when present, may also comprise antioxidant.
- antioxidant Although not wishing to be bound by theory, the Applicants believe that the presence of antioxidant reduced or preferably stops the reaction of reactive compounds in the formula e.g. perfumes, which tend to be oxidized over time and higher temperature and which can lead to yellowing.
- An antioxidant according to the present invention is a molecule capable of slowing or preventing the oxidation of other molecules. Oxidation reactions can produce free radicals, which in turn can start chain reactions of degradation. Antioxidants terminate these chain reactions by removing the free radical intermediates and inhibiting other oxidation reactions by being oxidized themselves. As a result antioxidants are often reducing agents.
- the antioxidant is preferably selected from the group consisting of butylated hydroxyl toluene (BHT), butylated hydroxyl anisole (BHA), trimethoxy benzoic acid (TMBA), ⁇ , ⁇ , ⁇ and ⁇ tocophenol (vitamin E acetate), 6 hydroxy-2,5,7,8 - tetra-methylchroman -2-carboxylic acid (trolox), 1,2, benzisothiazoline - 3-one (proxel GLX), tannic acid, galic acid, Tinoguard AO-6, Tinoguard TS, ascorbic acid, alkylated phenol, ethoxyquine 2,2,4 trimethyl, 1-2-dihydroquinoline, 2,6 di or tert or butyl hydroquinone, tert, butyl, hydroxyl anisole, lignosulphonic acid and salts thereof, benzofuran, benzopyran, tocopherol sorbate, butylated hydroxyl benzo
- the antioxidant is preferably present at a level of from 0.01% to 2%, more preferably from 0.1% to 1%, most preferably from 0.3% to 0.5% by weight of the compact liquid detergent composition.
- the opacifier and antioxidant are preferably present at a ratio of from 0.1 to 0.5, more preferably from 0.12 to 0.35. Whereas, where an organic opacifier is used, opacifier and antioxidant are preferably present at a ratio of from 2 to 6, more preferably from 3 to 5.
- the compact liquid detergent composition comprises a rheology modifier.
- the rheology modifier is selected from the group consisting of non-polymeric crystalline, hydroxy-functional materials, polymeric rheology modifiers which impart shear thinning characteristics to the aqueous liquid matrix of the composition.
- Crystalline, hydroxy-functional materials are rheology modifiers which form thread-like structuring systems throughout the matrix of the composition upon in situ crystallization in the matrix.
- Specific examples of preferred crystalline, hydroxyl-containing rheology modifiers include castor oil and its derivatives. Especially preferred are hydrogenated castor oil derivatives such as hydrogenated castor oil and hydrogenated castor wax.
- polymeric rheology modifiers are preferably selected from polyacrylates, polymeric gums, other non-gum polysaccharides, and combinations of these polymeric materials.
- Preferred polymeric gum materials include pectine, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, xanthan gum, guar gum and mixtures thereof.
- the compact liquid detergent compositions may comprise a fabric care benefit agent.
- fabric care benefit agent refers to any material that can provide fabric care benefits such as fabric softening, color protection, pill/fuzz reduction, anti-abrasion, anti-wrinkle, and the like to garments and fabrics, particularly on cotton and cotton-rich garments and fabrics, when an adequate amount of the material is present on the garment/fabric.
- fabric care benefit agents include cationic surfactants, silicones, polyolefin waxes, latexes, oily sugar derivatives, cationic polysaccharides, polyurethanes, fatty acids and mixtures thereof.
- Fabric care benefit agents when present in the compact liquid detergent composition are suitably at levels of up to 30% by weight of the compact liquid detergent composition, more typically from 1% to 20%, preferably from 2% to 10%.
- Suitable detersive enzymes for use herein include protease, amylase, lipase, cellulase, carbohydrase including mannanase and endoglucanase, and mixtures thereof. Enzymes can be used at their art-taught levels, for example at levels recommended by suppliers such as Novo and Genencor. Typical levels in the compact liquid detergent compositions are from 0.0001% to 5%. When enzymes are present, they can be used at very low levels, e.g., from 0.001% or lower, in certain embodiments of the invention; or they can be used in heavier-duty laundry detergent formulations in accordance with the invention at higher levels, e.g., 0.1% and higher. In accordance with a preference of some consumers for "non-biological" detergents, the present invention includes both enzyme-containing and enzyme-free embodiments.
- deposition aid refers to any cationic polymer or combination of cationic polymers that significantly enhance the deposition of a fabric care benefit agent onto the fabric during laundering.
- the deposition aid is a cationic or amphoteric polymer.
- the amphoteric polymers of the present invention will also have a net cationic charge, i.e.; the total cationic charges on these polymers will exceed the total anionic charge.
- Nonlimiting examples of deposition enhancing agents are cationic polysaccharides, chitosan and its derivatives and cationic synthetic polymers.
- Preferred cationic polysaccharides include cationic cellulose derivatives, cationic guar gum derivatives, chitosan and derivatives and cationic starches.
- the compact liquid detergent compositions may optionally comprise a builder.
- Suitable builders include polycarboxylate builders include cyclic compounds, particularly alicyclic compounds, such as those described in U.S. Patents 3,923,679 ; 3,835,163 ; 4,158,635 ; 4,120,874 and 4,102,903 .
- Particularly preferred are citrate builders, e.g., citric acid and soluble salts thereof (particularly sodium salt).
- Other preferred builders include aluminosilicates such as zeolite A, B or MAP; fatty acids or salts, preferably sodium salts, thereof, preferably C12-C18 saturated and/or unsaturated fatty acids; and alkali or alkali earth metal carbonates preferably sodium carbonate.
- the compact liquid detergent composition of the present application comprises from 2% to 20% fatty acids by weight of the compact liquid detergent composition, preferably from 5% to 15% fatty acids by weight of the compact liquid detergent composition and most preferably from 6% to 10% fatty acids by the weight of the compact liquid detergent composition.
- Bleaching agents suitable herein include chlorine and oxygen bleaches, especially inorganic perhydrate salts such as sodium perborate mono-and tetrahydrates and sodium percarbonate optionally coated to provide controlled rate of release (see, for example, GB-A-1466799 on sulfate/carbonate coatings), preformed organic peroxyacids and mixtures thereof with organic peroxyacid bleach precursors and/or transition metal-containing bleach catalysts (especially manganese or cobalt).
- Inorganic perhydrate salts are typically incorporated at levels in the range from 1% to 40% by weight, preferably from 2% to 30% by weight and more preferably from 5% to 25% by weight of compact liquid detergent composition.
- Peroxyacid bleach precursors preferred for use herein include precursors of perbenzoic acid and substituted perbenzoic acid; cationic peroxyacid precursors; peracetic acid precursors such as TAED, sodium acetoxybenzene sulfonate and pentaacetylglucose; pernonanoic acid precursors such as sodium 3,5,5-trimethylhexanoyloxybenzene sulfonate (iso-NOBS) and sodium nonanoyloxybenzene sulfonate (NOBS); amide substituted alkyl peroxyacid precursors ( EP-A-0170386 ); and benzoxazin peroxyacid precursors ( EP-A-0332294 and EP-A-0482807 ).
- Bleach precursors are typically incorporated at levels in the range from 0.5% to 25%, preferably from 1% to 10% by weight of composition while the preformed organic peroxyacids themselves are typically incorporated at levels in the range from 0.5% to 25% by weight, more preferably from 1% to 10% by weight of compact liquid detergent composition.
- Bleach catalysts preferred for use herein include the manganese triazacyclononane and related complexes ( US-A-4246612 , US-A-5227084 ); Co, Cu, Mn and Fe bispyridylamine and related complexes ( US-A-5114611 ); and pentamine acetate cobalt(III) and related complexes( US-A-4810410 ).
- a compact liquid detergent composition may comprise a whitening agent.
- a whitening agent Such dyes have been found to exhibit good tinting efficiency during a laundry wash cycle without exhibiting excessive undesirable build up during laundering.
- the whitening agent is included in the total laundry detergent composition in an amount sufficient to provide a tinting effect to fabric washed in a solution containing the detergent.
- a multi-compartment pouch comprises, by weight, from 0.0001% to 1%, more preferably from 0.0001% to 0.5% by weight of the compact liquid detergent composition, and even more preferably from 0.0001% to 0.3% by weight of the compact liquid detergent composition.
- the compact liquid detergent compositions of the present invention may comprise a pearlescent agent.
- Said pearlescent agent may be organic or inorganic, but is preferably inorganic. Most preferably the pearlescent agent is selected from mica, TiO 2 coated mica, bismuth oxychloride or mixtures thereof.
- Perfumes are preferably incorporated into the compact liquid detergent compositions of the present invention.
- the perfumes may be prepared as a premix liquid, may be linked with a carrier material, such as cyclodextrin or may be encapsulated.
- a carrier material such as cyclodextrin
- cleaning adjunct materials include, but are not limited to; enzyme stabilizing systems; scavenging agents including fixing agents for anionic dyes, complexing agents for anionic surfactants, and mixtures thereof; optical brighteners or fluorescers; soil release polymers; dispersants; suds suppressors; dyes; colorants; hydrotropes such as toluenesulfonates, cumenesulfonates and naphthalenesulfonates; color speckles; colored beads, spheres or extrudates; clay softening agents and mixtures thereof.
- the compact detergent compositions herein can generally be prepared by mixing the ingredients together. If a pearlescent material is used it should be added in the late stages of mixing. If a rheology modifier is used, it is preferred to first form a pre-mix within which the rheology modifier is dispersed in a portion of the water and optionally other ingredients eventually used to comprise the compositions. This pre-mix is formed in such a way that it forms a structured liquid. To this structured pre-mix can then be added, while the pre-mix is under agitation, the surfactant(s) and essential laundry adjunct materials, along with water and whatever optional detergent composition adjuncts are to be used.
- the pouch is preferably made of a film material which is soluble or dispersible in water, and has a water-solubility of at least 50%, preferably at least 75% or even at least 95%.
- the water-solubility is measured by the method set out here after using a glass-filter with a maximum pore size of 20 microns: 50 grams ⁇ 0.1 gram of pouch material is added in a pre-weighed 400 ml beaker and 245ml ⁇ 1ml of distilled water is added. This is stirred vigorously on a magnetic stirrer set at 600 rpm, for 30 minutes.
- the mixture is filtered through a folded qualitative sintered-glass filter with a pore size as defined above (max. 20 micron).
- the water is dried off from the collected filtrate by any conventional method, and the weight of the remaining material is determined (which is the dissolved or dispersed fraction). Then, the percentage solubility or dispersability can be calculated.
- Preferred pouch materials are polymeric materials, preferably polymers which are formed into a film or sheet.
- the pouch material can, for example, be obtained by casting, blow-moulding, extrusion or blown extrusion of the polymeric material, as known in the art.
- Preferred polymers, copolymers or derivatives thereof suitable for use as pouch material are described in WO03/045812 (Procter & Gamble Company), WO04/085586 (Procter & Gamble Company) and WO07/130684 (Procter & Gamble Company).
- the level of polymer in the pouch material is at least 60%.
- the polymer can have any weight average molecular weight, preferably from 1000 to 1,000,000, more preferably from 10,000 to 300,000 yet more preferably from 20,000 to 150,000.
- Mixtures of polymers can also be used as the pouch material. This can be beneficial to control the mechanical and/or dissolution properties of the compartments or pouch, depending on the application thereof and the required needs.
- Suitable mixtures include for example mixtures wherein one polymer has a higher water-solubility than another polymer, and/or one polymer has a higher mechanical strength than another polymer. Also suitable are mixtures of polymers having different weight average molecular weights.
- compartments of the present invention may be employed in making the compartments of the present invention.
- a benefit in selecting different films is that the resulting compartments may exhibit different solubility or release characteristics.
- Most preferred pouch materials are PVA films known under the trade reference Monosol M8630, as sold by MonoSol LLC of Gary, Indiana, US, and PVA films of corresponding solubility and deformability characteristics.
- Other films suitable for use herein include films known under the trade reference PT film or the K-series of films supplied by Aicello, or VF-HP film supplied by Kuraray.
- the pouch material herein can also comprise one or more additive ingredients.
- plasticisers for example glycerol, ethylene glycol, diethyleneglycol, propylene glycol, sorbitol and mixtures thereof.
- Other additives include functional detergent additives to be delivered to the wash water, for example organic polymeric dispersants, etc.
- pouches or pouch compartments containing a component which is liquid will preferably contain an air bubble having a volume of up to 50%, preferably up to 40%, more preferably up to 30%, more preferably up to 20%, more preferably up to 10% of the volume space of said compartment.
- the process of making the water-soluble pouch may be made using any suitable equipment and method.
- Single compartment pouches are made using vertical, but preferably horizontal form filling techniques commonly known in the art.
- the multi-compartment pouches of the present invention are preferably further packaged in an outer package.
- Said outer package may be a see-through or partially see-through container, for example a transparent or translucent bag, tub, carton or bottle.
- the pack can be made of plastic or any other suitable material, provided the material is strong enough to protect the pouches during transport. This kind of pack is also very useful because the user does not need to open the pack to see how many pouches there are left.
- the pack can have non-see-through outer packaging, perhaps with indicia or artwork representing the visually-distinctive contents of the pack.
- the compact liquid detergent of the present invention is suitable for laundry cleaning applications.
- the compact liquid detergent is suitable for hand or machine washing conditions.
- the compact liquid detergent may be delivered from the dispensing drawer or may be added directly into the washing machine drum either in a form of water-soluble pouches or in a form of compact liquid.
- composition A Composition B
- Ingredient Name WT% WT% Linear Alkyl benzene sulfonic acid 16 14 C12-14 alkyl ethoxy 3-sulfate MEA salt 10 13 C12-14 alkyl 7-ethoxylate 9 15 C 12-18
- Fatty acid 15 8
- Solvent 15 14 Buffer (Monoethanol amine) To pH 7.5 To pH 7.5 Water 10 15 Miscellaneous/Minors to 100 to 100 1 H-EDDS: Ethylenediamine-N,N'-disuccinic acid
- the performance of the chelants were measured on wine and tea.
- Wine and tea stains were applied to cotton and obtained from EMC (US). Stains and ballast load consisting of 0.5kg of T-shirt was added to a MiniWasher representing a medium US wash conditions.
- the wash water was set at 32.2 °C ⁇ 1 °C and 6gpg (1mmol/L) hardness and the rinse water was set at 15.5 °C ⁇ 1 °C.
- the water volume was 15 liters and wash time 12 minutes.
- SRI stain removal index
- the Laundry Image Analysis system measures stain removal on technical stain swatches.
- the system utilizes a video camera to acquire color images of swatches. An image of the swatch is taken before and after it is washed. The acquired image is then analyzed by computer software (Global R&D computing). The software compares the unwashed stain to the washed stain, as well as the unwashed fabric to the washed fabric and produces five figures of merit which describe stain removal. The data are then analyzed statistically to determine statistically significant differences between the detergent performances.
- the stain removal index uses the initial fabric as the reference against which to measure color differences between unwashed and washed stains. A higher value indicates a better cleaning and stain removal thus a better detergent.
- the standard deviation is 1. Stain Removal Index Stain Removal Index Nil Chelant 54.6 22.8 Chelant Wine Tea Na-DTPA - 1ppm 55.2 27.6 Na-DTPA - 2 ppm 55.8 29.0 Na-DTPA - 3 ppm 56.4 27.1 Na-EDDS - 1 ppm 58.3 28.2 Na-EDDS - 2 ppm 59.0 29.3 Na-EDDS - 3 ppm 56.8 26.1 Na-DTPA(0.5ppm) 57.1 28.7 Na-EDDS (0.5 ppm) Na-DTPA (1ppm) 58.9 32.4 Na-EDDS (1ppm) Na-DTPA (1.5 ppm) 59.9 33.9 Na-EDDS (1.5 ppm)
- Products (I through III) were prepared by combining Composition C and the 3 different chelant combinations.
- the products (75g) were stored for 4 weeks at 4°C, 20°C and 35°C in a Glass Jar (100mL kie).
- the product stability was then assessed visually. If there is a visual precipitate or a product phase split, the stability is considered Fail. Stability is considered Pass if there is no signs of changes during the storage period.
- Composition C Ingredient Name WT% Linear Alkyl benzene sulfonic acid 16 C12-14 alkyl ethoxy 3 sulfate MEA salt 10 C12-14 alkyl 7-ethoxylate 9 C12-18 Fatty acid 15 Enzymes 2.3 Solvent 15 Monoethanol amine To pH 7.5 Water 10 Miscellaneous/Minors to 100 Product Chelant Pass/Fail I Na-DTPA - 0.7% Pass II Na-DTPA - 1.4% Fail III Na-EDDS/Na-DTPA (0.7%/0.7 %) Pass
- the stability test shows the synenergy between the chelants DTPA and EDDS.
- a compact liquid detergent composition comprising 0.7% of Na-DTPA is stable, however it does not provide desired cleaning efficacy. By increasing the quantity of Na-DTPA to the effective level, the composition does not meet the stability requirements. Combination of 0.7% Na-EDDS and 0.7% Na-DTPA does provide desired cleaning efficacy and meets the stability requirements.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL10748205T PL2334776T3 (pl) | 2009-09-15 | 2010-08-26 | Kompozycja detergentu zawierająca mieszaninę środków chelatujących |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24240709P | 2009-09-15 | 2009-09-15 | |
PCT/US2010/046716 WO2011034701A1 (en) | 2009-09-15 | 2010-08-26 | Detergent composition comprising mixture of chelants |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2334776A1 EP2334776A1 (en) | 2011-06-22 |
EP2334776B1 true EP2334776B1 (en) | 2012-11-14 |
Family
ID=43086222
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10748205A Not-in-force EP2334776B1 (en) | 2009-09-15 | 2010-08-26 | Detergent composition comprising mixture of chelants |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP2334776B1 (es) |
JP (1) | JP5133460B2 (es) |
CN (1) | CN102549135A (es) |
AR (1) | AR078366A1 (es) |
BR (1) | BR112012005841A2 (es) |
CA (1) | CA2770477C (es) |
ES (1) | ES2399703T3 (es) |
MX (1) | MX2012003186A (es) |
PL (1) | PL2334776T3 (es) |
RU (1) | RU2499817C2 (es) |
WO (1) | WO2011034701A1 (es) |
ZA (1) | ZA201202653B (es) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10538631B2 (en) | 2016-09-13 | 2020-01-21 | The Procter & Gamble Company | Benefit agent containing delivery particle |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103196857A (zh) * | 2013-04-19 | 2013-07-10 | 陈军 | 洗涤评估用人工污渍样本的制备方法 |
JP6594419B2 (ja) * | 2014-10-17 | 2019-10-23 | ビーエーエスエフ ソシエタス・ヨーロピア | Mgda含有の洗剤組成物を包んだ包装体 |
EP3026102B1 (en) * | 2014-11-26 | 2018-12-26 | The Procter and Gamble Company | Cleaning pouch |
ES2690336T3 (es) * | 2014-11-26 | 2018-11-20 | The Procter & Gamble Company | Bolsa limpiadora |
ES2690335T3 (es) * | 2014-11-26 | 2018-11-20 | The Procter & Gamble Company | Bolsa limpiadora |
PL3026099T3 (pl) * | 2014-11-26 | 2021-06-14 | The Procter & Gamble Company | Saszetka czyszcząca |
US20170369819A1 (en) * | 2016-06-27 | 2017-12-28 | The Procter & Gamble Company | Removal of hydrophilic body soils |
EP3594319B1 (en) * | 2018-07-12 | 2021-05-05 | The Procter & Gamble Company | A solid free-flowing particulate laundry detergent composition |
EP3733826B1 (en) * | 2019-05-03 | 2024-07-17 | The Procter & Gamble Company | Particle treatment compositions comprising an antioxidant |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2220099A (en) | 1934-01-10 | 1940-11-05 | Gen Aniline & Flim Corp | Sulphonic acids |
US2477383A (en) | 1946-12-26 | 1949-07-26 | California Research Corp | Sulfonated detergent and its method of preparation |
US3664961A (en) | 1970-03-31 | 1972-05-23 | Procter & Gamble | Enzyme detergent composition containing coagglomerated perborate bleaching agent |
FR2226460B1 (es) | 1973-04-20 | 1976-12-17 | Interox | |
US3835163A (en) | 1973-08-02 | 1974-09-10 | Monsanto Co | Tetrahydrofuran polycarboxylic acids |
US3919678A (en) | 1974-04-01 | 1975-11-11 | Telic Corp | Magnetic field generation apparatus |
US4102903A (en) | 1977-01-05 | 1978-07-25 | Monsanto Company | Tetrahydropyran and 1,4-dioxane polycarboxylate compounds, methods for making such compounds and compositions and methods employing same |
US4120874A (en) | 1977-01-05 | 1978-10-17 | Monsanto Company | Diesters of 6-cyano-2,2-tetrahydropyrandicarboxylates |
US4222905A (en) | 1978-06-26 | 1980-09-16 | The Procter & Gamble Company | Laundry detergent compositions having enhanced particulate soil removal performance |
US4158635A (en) | 1977-12-05 | 1979-06-19 | Monsanto Company | Detergent formulations containing tetrahydropyran or 1,4-dioxane polycarboxylates and method for using same |
US4239659A (en) | 1978-12-15 | 1980-12-16 | The Procter & Gamble Company | Detergent compositions containing nonionic and cationic surfactants, the cationic surfactant having a long alkyl chain of from about 20 to about 30 carbon atoms |
GB2048606B (en) | 1979-02-28 | 1983-03-16 | Barr & Stroud Ltd | Optical scanning system |
GB8415909D0 (en) | 1984-06-21 | 1984-07-25 | Procter & Gamble Ltd | Peracid compounds |
GB8629837D0 (en) | 1986-12-13 | 1987-01-21 | Interox Chemicals Ltd | Bleach activation |
GB8803114D0 (en) | 1988-02-11 | 1988-03-09 | Bp Chem Int Ltd | Bleach activators in detergent compositions |
GB8908416D0 (en) | 1989-04-13 | 1989-06-01 | Unilever Plc | Bleach activation |
GB9023000D0 (en) | 1990-10-23 | 1990-12-05 | Bp Chem Int Ltd | Barrier coatings |
GB9108136D0 (en) | 1991-04-17 | 1991-06-05 | Unilever Plc | Concentrated detergent powder compositions |
ES2185764T3 (es) * | 1995-02-28 | 2003-05-01 | Procter & Gamble | Pretratamiento de la colada con agentes de blanqueo peroxigenados que contienen agentes quelantes para hierro, cobre o manganeso para reducir el daño al tejido. |
CA2264555A1 (en) * | 1996-09-27 | 1998-04-02 | Unilever Plc | Aqueous structured liquid detergent composition comprising aminocarboxylate sequestrant |
WO1999002636A1 (en) * | 1997-07-11 | 1999-01-21 | The Procter & Gamble Company | Detergent compositions comprising a specific cellulase and a nil-phosphate containing chelant |
GB2329188A (en) * | 1997-09-11 | 1999-03-17 | Procter & Gamble | Detergent composition containing a stabilised percarboxylic bleaching system |
WO2001083668A1 (en) | 2000-04-28 | 2001-11-08 | The Procter & Gamble Company | Pouched compositions |
AU2001263062A1 (en) | 2000-05-11 | 2001-11-20 | The Procter And Gamble Company | Highly concentrated fabric softener compositions and articles containing such compositions |
GB2369083A (en) | 2000-11-17 | 2002-05-22 | Procter & Gamble | Process for preparing pouches |
ES2279287T5 (es) | 2000-11-27 | 2015-10-20 | The Procter & Gamble Company | Envase para detergente |
GB2373254A (en) | 2001-03-16 | 2002-09-18 | Procter & Gamble | Detergent product |
EP1314652B1 (en) | 2001-11-23 | 2006-03-08 | The Procter & Gamble Company | Water-soluble pouch |
US20040186035A1 (en) | 2003-03-19 | 2004-09-23 | The Procter & Gamble Company | Water-soluble, liquid-containing pouch |
US20080015135A1 (en) * | 2006-05-05 | 2008-01-17 | De Buzzaccarini Francesco | Compact fluid laundry detergent composition |
WO2007130684A1 (en) | 2006-05-05 | 2007-11-15 | The Procter & Gamble Company | Films with microcapsules |
US8519060B2 (en) | 2006-05-31 | 2013-08-27 | Basf Se | Amphiphilic graft polymers based on polyalkylene oxides and vinyl esters |
GB0714575D0 (en) | 2007-07-26 | 2007-09-05 | Innospec Ltd | Composition |
GB0714569D0 (en) | 2007-07-26 | 2007-09-05 | Innospec Ltd | Composition |
-
2010
- 2010-08-26 PL PL10748205T patent/PL2334776T3/pl unknown
- 2010-08-26 ES ES10748205T patent/ES2399703T3/es active Active
- 2010-08-26 EP EP10748205A patent/EP2334776B1/en not_active Not-in-force
- 2010-08-26 MX MX2012003186A patent/MX2012003186A/es unknown
- 2010-08-26 RU RU2012105130/04A patent/RU2499817C2/ru not_active IP Right Cessation
- 2010-08-26 JP JP2011535801A patent/JP5133460B2/ja not_active Expired - Fee Related
- 2010-08-26 CA CA2770477A patent/CA2770477C/en not_active Expired - Fee Related
- 2010-08-26 WO PCT/US2010/046716 patent/WO2011034701A1/en active Application Filing
- 2010-08-26 BR BR112012005841A patent/BR112012005841A2/pt not_active IP Right Cessation
- 2010-08-26 CN CN2010800419123A patent/CN102549135A/zh active Pending
- 2010-09-14 AR ARP100103346A patent/AR078366A1/es active IP Right Grant
-
2012
- 2012-04-12 ZA ZA2012/02653A patent/ZA201202653B/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10538631B2 (en) | 2016-09-13 | 2020-01-21 | The Procter & Gamble Company | Benefit agent containing delivery particle |
US10556995B2 (en) | 2016-09-13 | 2020-02-11 | The Procter & Gamble Company | Process for making a composition comprising benefit agent delivery particles |
Also Published As
Publication number | Publication date |
---|---|
BR112012005841A2 (pt) | 2019-09-24 |
WO2011034701A1 (en) | 2011-03-24 |
EP2334776A1 (en) | 2011-06-22 |
CN102549135A (zh) | 2012-07-04 |
ES2399703T3 (es) | 2013-04-02 |
CA2770477C (en) | 2014-07-08 |
RU2012105130A (ru) | 2013-10-27 |
PL2334776T3 (pl) | 2013-04-30 |
AR078366A1 (es) | 2011-11-02 |
MX2012003186A (es) | 2012-04-30 |
ZA201202653B (en) | 2014-10-29 |
JP2012508307A (ja) | 2012-04-05 |
JP5133460B2 (ja) | 2013-01-30 |
RU2499817C2 (ru) | 2013-11-27 |
CA2770477A1 (en) | 2011-03-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2334776B1 (en) | Detergent composition comprising mixture of chelants | |
CA2770037C (en) | Detergent composition comprising surfactant boosting polymers | |
US8629093B2 (en) | Detergent composition comprising mixture of chelants | |
EP2258820B1 (en) | Water-soluble pouch | |
EP2130897B1 (en) | Surfactant concentrate | |
US20030148908A1 (en) | Detergent package | |
WO2015148461A1 (en) | Printed water soluble pouch | |
CA2491057C (en) | A detergent composition comprising an amine oxide surfactant | |
EP3004305A1 (en) | Concentrated surfactant composition | |
EP2295530B2 (en) | Detergent composition | |
AU715749B2 (en) | Aqueous structured liquid detergent composition comprising aminocarboxylate sequestrant | |
EP1378562A1 (en) | Detergent compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20110407 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME RS |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
DAX | Request for extension of the european patent (deleted) | ||
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP Ref country code: AT Ref legal event code: REF Ref document number: 584028 Country of ref document: AT Kind code of ref document: T Effective date: 20121115 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602010003644 Country of ref document: DE Effective date: 20130110 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2399703 Country of ref document: ES Kind code of ref document: T3 Effective date: 20130402 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: VDEP Effective date: 20121114 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 584028 Country of ref document: AT Kind code of ref document: T Effective date: 20121114 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130214 |
|
REG | Reference to a national code |
Ref country code: PL Ref legal event code: T3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130215 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130314 Ref country code: BE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130214 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
REG | Reference to a national code |
Ref country code: HU Ref legal event code: AG4A Ref document number: E016593 Country of ref document: HU |
|
26N | No opposition filed |
Effective date: 20130815 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20130822 Year of fee payment: 4 Ref country code: CZ Payment date: 20130815 Year of fee payment: 4 Ref country code: HU Payment date: 20130726 Year of fee payment: 4 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: PL Payment date: 20130808 Year of fee payment: 4 Ref country code: FR Payment date: 20130725 Year of fee payment: 4 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602010003644 Country of ref document: DE Effective date: 20130815 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20130831 Year of fee payment: 4 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130826 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20130902 Year of fee payment: 4 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602010003644 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20140826 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140826 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140831 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140831 Ref country code: CZ Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140826 Ref country code: HU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140827 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20150430 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602010003644 Country of ref document: DE Effective date: 20150303 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130826 Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20150303 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140826 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140901 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20150925 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140827 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140826 |
|
REG | Reference to a national code |
Ref country code: PL Ref legal event code: LAPE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20121114 |