EP2195410A1 - Performance ingredients in film particles - Google Patents
Performance ingredients in film particlesInfo
- Publication number
- EP2195410A1 EP2195410A1 EP08804761A EP08804761A EP2195410A1 EP 2195410 A1 EP2195410 A1 EP 2195410A1 EP 08804761 A EP08804761 A EP 08804761A EP 08804761 A EP08804761 A EP 08804761A EP 2195410 A1 EP2195410 A1 EP 2195410A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- film
- detergent composition
- granular detergent
- composition according
- preferred
- 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.)
- Granted
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
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/02—Floating bodies of detergents or of soaps
-
- 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
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0063—Photo- activating compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0084—Antioxidants; Free-radical scavengers
-
- 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
- C11D3/3753—Polyvinylalcohol; Ethers or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3935—Bleach activators or bleach catalysts granulated, coated or protected
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
-
- 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
Definitions
- This invention relates to granular detergent compositions comprising a plurality of film particles.
- the contrasting particles may deliver a functional ingredient or may simply provide a visual cue to the user.
- a minor proportion of contrastingly colored elongated soap particles is added to a detergent powder.
- the contrasting particles comprise a non fabric-substantive dye and a fluorescer.
- the powder comprises a detergency builder compound.
- the soap particles contribute detergency to the composition and reduce foaming. Because the soap particles could sink onto the fabric it is a stated advantage of the particles that they do not cause staining of the fabric with which they come into contact.
- a powder detergent composition having a major proportion of white or light-coloured particles has dry mixed into it a minor proportion of lamellar visually contrasting bodies of significantly larger average particle size in at least one dimension than the average particle size of the white or light-coloured particles.
- the visually contrasting bodies may optionally contain detergent functional ingredients.
- WO2006/079416 proposes to use a highly soluble film particle as a visual cue. It is suggested to be possible to include functional ingredients within the film e.g. surface active agents, perfume, antioxidant, antifoam. Examples in this application compare detergent powders containing 0.1 wt% visual cues made from polyvinyl alcohol with visual cues made from gum Arabic. Suitably, the film particles could be chosen to pass a 1400 ⁇ m sieve, but not a 500 ⁇ m sieve.
- US4176079 describes an alternative to post dosing granules.
- An enzyme is incorporated into a water soluble film and the functional film so produced is cut into squares, rectangles or strips and added to a detergent powder.
- Typical film additive compositions are polyvinyl alcohol 48.7 % and nonionic surfactant 43.8 % (balance water and enzyme) .
- the cut functional film additive has a surface area of 300 mm 2 .
- US 2005/0075261 Al relates to a water-soluble and/or water dispersible particle comprising an active ingredient, preferably an enzyme, in a matrix comprising from 20-95% of the particle of a specified polyvinylalcohol polymer.
- the examples make the particle by applying a chopping action to an extruded noodle. This would tend to make a granular (spherical) particle.
- Other active ingredients suggested for inclusion at levels of 0.1 to 55% include: bleaches, bleach activators, bleach catalysts, brighteners and photobleaches .
- the particle size ranges from 200 ⁇ m to 2000 ⁇ m, preferably 250 ⁇ m to 800 ⁇ m.
- the extruded (cylindrical) particle is not chopped up it can be up to 20mm long, but it is preferably less than lmm long and has a preferred particle size distribution of lOO ⁇ m to 800 ⁇ m.
- a major problem is to make a visual cue film particle that aids cleaning. Surprisingly, we have now found new benefits from delivery of specific benefit ingredients from a film particle .
- a granular detergent composition comprising a plurality of film particles, each film particle comprising at least 30% polymer and 0.01 to lwt% of a benefit ingredient selected from the group comprising: shading dye, shading pigment, photobleach, fluorescer, antioxidant, transition metal catalyst and mixtures thereof characterised in that the thickness of each film particle is less than 0.5 mm and the cross sectional area of each film particle is between 4 mm 2 and 100mm 2 .
- Granular laundry detergent compositions are mainly composed of surfactants and electrolytes.
- Typical surfactants include linear alkyl benzene sulphonates, primary alcohol sulphates, linear alcohol ethoxysulphates and alcohol ethoxylates.
- Typical electrolytes are inorganic materials such as sodium sulphate, sodium chloride, sodium tripolyphosphates, sodium carbonate, silicas, and zeolites and organic materials such as polycarboxylates and citric acid.
- benefit ingredients namely fluorescers, shading dyes, photobleaches antioxidant and catalysts
- benefit ingredients may be included at low levels.
- Such benefit ingredients are most cost-effective when added at very low levels, typically less than 0. lwt% of the composition.
- the benefit ingredients are usually granulated and then post- dosed into the granular composition. This inevitably results in localised high concentrations of the benefit ingredient, which can cause problems if they come into contact with certain fabrics before they have had an opportunity to dissolve or disperse into the wash liquor. This problem is caused by the localised high concentration of the benefit ingredient and not by the timing of its release.
- the problem occurs particularly for low molecular weight benefit ingredients that cause damage to fabrics when present at very high concentrations, particularly if delivered from a carrier substrate that has a higher solubility and/or dispersibilty than the benefit ingredient.
- the amount of benefit ingredient in the film particle is preferably 0.05 to 1.0 wt% of the film particle .
- the film particles are desirably rendered visible by non fabric-substantive dye that gives them a contrasting colour from the granules making up the remainder of the granular composition .
- Granular detergent compositions of lighter colour than the film particles advantageously include some fluorescer and/or shading dye in the granules to give a higher contrast between the granules and the film particles.
- the granular detergent composition is preferably highly alkaline when dissolved in deionised water.
- a 0.1% solution at 25 0 C is > pH 10.5.
- the granular detergent composition may advantageously comprise silicate and/or carbonate.
- the film particle is preferably more near to a neutral pH to protect the benefit ingredient or ingredients contained therein. It has a pH of 3 to 9, preferably 6 to 8 when dissolved to form a 0.1% solution in deionised water. Although many soluble polymers could be suitable for inclusion in the film particle, a preferred polymeric material is polyvinyl alcohol. To improve its solubility and to facilitate easy inclusion of the benefit ingredients the film particles desirably further comprise 5 to 50 wt% surfactant. Preferred surfactant content of the film particles is at least 5 wt% anionic surfactant, most preferably an alkyl sulphate.
- Preferred film compositions are those that comprise a polymer and a surfactant.
- a colorant is also included as a preferred ingredient of the film, in addition to the performance ingredient.
- adjuncts to assist in the manufacture of the film for instance release agents and water.
- water also assists in plasticising the film and regulates its solubility.
- the polymer may be selected from water soluble film forming polymers, especially those used in formulation of detergent powders.
- Preferred polymers include polymers which dissolve and/disperse completely in water within 30 minutes with agitation at a temperature anywhere in the range of from 293 to 333K.
- Preferred water soluble polymers are those capable of being cast into a film or solid mass, for example as described in Davidson and Sittig, Water-Soluble Resins, Van Nostrand
- Preferred water-soluble resins include polyvinyl alcohol, cellulose ethers, polyethylene oxide, starch, polyvinylpyrrolidone, polyacrylamide, polyvinyl methyl ether-maleic anhydride, polymaleic anhydride, styrene maleic anhydride, hydroxyethylcellulose, hydroxypropylmethylcellulose, polyethylene glycols, carboxymethylcellulose, polyacrylic acid salts, alginates, acrylamide copolymers, guar gum, casein, ethylene-maleic anhydride resin series, polyethyleneimine, ethyl hydroxyethylcellulose, ethyl methylcellulose, hydroxyethyl methylcellulose, sugars. Lower molecular weight water-soluble, polyvinyl alcohol film- forming resins are preferred.
- Polyvinyl alcohols preferred for use therein have an average molecular weight anywhere between 1,000 and 1,000,000, preferably between 5,000 and 250,000, for example between 15,000 and 150,000.
- Hydrolysis, or alcoholysis is defined as the percent completion of the reaction where acetate groups on the resin are substituted with hydroxyl, -OH, groups,
- a hydrolysis range of from 60-99% of polyvinyl alcohol film-forming resin is preferred, while a more preferred range of hydrolysis is from about 70-90% for water-soluble, polyvinyl alcohol film-forming resins. The most preferred range of hydrolysis is 80-89%.
- polyvinyl alcohol includes polyvinyl acetate compounds with levels of hydroloysis disclosed herein.
- Another suitable polymer is a polyvinyl alcohol film, made of a polyvinyl alcohol copolymer having a comonomer having a carboxylate function.
- the preferred grade of PVA picks up water only at an RH well above that of granular detergent compositions. Thereby, it protects the other film ingredients from decomposition by water and soluble dyes from bleeding.
- the visual cue film particle may comprise 10 to 80% polymer or polymer mixture.
- the surfactant is preferably an anionic surfactant, especially if the granular composition comprises a builder.
- Suitable anionic surfactants include are well-known to those skilled in the art.
- Examples of high-foaming sulphonate or sulphate type surfactants include alkylbenzene sulphonates, particularly linear alkylbenzene sulphonates having an alkyl chain length of Cs-Ci 5 ; primary and secondary alkylsulphates, particularly Cs-Ci 5 primary alkyl sulphates; olefin sulphonates; alkyl xylene sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
- Sodium salts are generally preferred.
- the preferred anionic surfactants are alkylbenzene sulphonates, more especially linear alkylbenzene sulphonate (LAS) , which is preferably present in an amount of from 12 to 24 wt%, more preferably from 12 to 22 wt% and especially from 15 to 22 wt%.
- LAS linear alkylbenzene sulphonate
- Even more preferred are primary alcohol sulphates (PAS) , particularly Cs-Cis, preferably C12-C15, primary alcohol sulphates.
- a particularly preferred surfactant is primary alcohol sulphate (PAS) with a carbon chain length of 12. Visual cue Film particles containing up to 50 % PAS, may be used.
- the film may additionally include a second surfactant.
- the second surfactant is preferably chosen from amphoteric surfactants, zwitterionic surfactants, nonionic surfactants and ethoxylated anionic surfactants.
- Preferred amphoteric second surfactants are amine oxides.
- the most preferred amine oxide is coco dimethylamine oxide.
- Preferred zwitterionic second surfactants are betaines, and especially amidobetaines, for example, coco amidopropyl betaine .
- Preferred nonionic second surfactants include the primary and secondary alcohol ethoxylates, especially the C8-C20 aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C10-C15 primary and secondary aliphatic alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol.
- Preferred ethoxylated anionic second surfactants include alkyl ether sulphates (ethoxylated alcohol sulphates) .
- alkyl ether sulphates ethoxylated alcohol sulphates
- Cs-Cis alkyl monoethanolamides for example, coco monoethanolamide .
- the second surfactant system used in the film particle may additionally comprise minor amounts, e.g. less than 5% of the film, of cationic surfactant.
- Surfactant may be included at a level of up to 90 wt%, preferably up to 75 wt%, most preferably up to 60 wt% in the film.
- Non fabric-substantive colorants may be included in the film composition at a level of 0.001 to 0.5 wt%, preferably 0.1 to 0.3 wt% of the film.
- Suitable colorants include any that are used to colour detergent liquids or powders. Yellow, blue, violet, purple, red, orange, green, pink are preferred colours.
- This problem may be overcome by incorporating the benefit ingredients in a soluble polymer film that is then cut into discrete pieces having a low cross sectional area of less than 100mm 2 .
- Such film particles may also serve the purpose of visual cues if they also include dye. Their function as a visual cue may be further enhanced by cutting the film particles into the shape of a flower with petals, or some other such natural object.
- the cross-sectional area should be at least 4mm 2 . By cross-sectional area we mean the actual surface area of one side of the planar film particle.
- the film particles have the additional advantage of keeping the often sensitive benefit ingredients away from the aggressive high pH of a base laundry detergent composition. It provides a clear visual cue to the user that the benefit ingredient is present. It is particularly desirable that the film particle floats when first added to water. This enhances the visibility of the film particle in use and can also assist with the reduction of spotting or other fabric damage due to the initial dissolution taking place on the surface, which is likely to be remote from most of the fabrics being washed. To ensure that the film particle floats it is preferred that its relative density is less than 0.8, more preferably less than 0.5 and most preferably less than 0.4.
- the thickness of the planar film of the film particle is at most 0.5mm. Preferably it is less than 0.3mm, most preferably 0.2mm.
- the film is of relatively uniform thickness to allow predictable dissolution characteristics.
- the thickness tolerance is at most plus or minus 20%, preferably plus or minus 10%.
- the film particles comprise 0.01 to 1 wt% of a benefit ingredient selected from shading dye and pigment, for fabric whiteness.
- the shading dye, or pigment is selected from:
- Pigments are coloured particles preferably of 0.05 to 10 micron size, which are practically insoluble in aqueous media that contain surfactants. Preferred pigments are blue or violet.
- pigment blue 29 or pigment violet 15 may be used, however, organic pigments are preferred.
- Preferred organic pigments are pigment violet 1, 1:1, 1:2, 2, 3, 5:1, 13, 19, 23, 25, 27, 31, 32, 37, 39, 42, 44, 50 and Pigment blue 1, 2, 9, 10, 14, 15, 15:1, 15:2, 15:3, 15:4, 15:6, 16, 18, 19, 24:1, 25, 56, 60, 61, 62, 66, 75, 79 and 80. More preferred pigments are pigment violet 3, 13, 23, 27, 37, 39, pigment blue 14, 25, 66 and 75.
- pigment violet 23 The most preferred is pigment violet 23.
- White pigments may also be used; these are especially suitable if the granular detergent composition is a deep hue, for example green or blue. Suitable White pigments are listed in the color index (Society of Dyers and Colourists and American Association of Textile Chemists and Colorists 2002 ), pigment white 1 through pigment white 35 may be used to whiten the petal. Preferred are pigment white 18, pigment white 26, pigment white 27, pigment white 6, pigment white 4 and metal stearate salts where the metals are selected from Ba, Ca, Mg or Zn .
- White pigments are described in detail in ' Industrial Inorganic Pigments' (3rd edition 2005 G.Buxbaum, G.Pfaff eds, Wiley VCH) and include TiO2, zinc white (ZnO), zinc sulfide and lithopone.
- Direct violet and direct blue dyes are even more preferred than pigments.
- the dyes are bis or tris - azo dyes.
- the carcinogenic benzidene based dyes are not preferred.
- the direct dye is a direct violet of the following structure
- Ri is hydrogen or alkyl
- R2 is hydrogen, alkyl or substituted or unsubstituted aryl, preferably phenyl
- R3 and R4 are independently hydrogen or alkyl
- n is 0, 1 or 2, preferably 1 or 2.
- Preferred dyes are direct violet 7, direct violet 9, direct violet 11, direct violet 26, direct violet 31, direct violet
- the direct dye may be covalently linked to a photobleach, for example as described in WO2006/024612.
- Cotton substantive acid dyes give benefits to cotton containing fabrics.
- Preferred dyes and mixes of dyes are blue or violet.
- Preferred acid dyes are:
- R a , R b , R c and R d are selected from: H, a branched or linear Cl to C7-alkyl chain, benzyl, a phenyl, and a naphthyl; the dye is substituted with at least one S ⁇ 3 ⁇ or - COO ⁇ group; the B ring does not carry a negatively charged group or salt thereof; and the A ring may further substituted to form a naphthyl; the dye is optionally substituted by groups selected from: amine, methyl, ethyl, hydroxyl, methoxy, ethoxy, phenoxy, Cl, Br, I, F, and NO2.
- Preferred azine dyes are: acid blue 98, acid violet 50, and acid blue 59, more preferably acid violet 50 and acid blue 98.
- the benefit ingredient may comprise one or more hydrophobic dyes selected from benzodifuranes, methine, triphenylmethanes, napthalimides, pyrazole, napthoquinone, anthraquinone and mono-azo or di-azo dye chromophores .
- Hydrophobic dyes are dyes that do not contain any charged water solubilising group. Hydrophobic dyes may be selected from the groups of disperse and solvent dyes. Blue and violet anthraquinone and mono-azo dye are preferred.
- Preferred dyes include solvent violet 13, disperse violet 27 disperse violet 26, disperse violet 28, disperse violet 63 and disperse violet 77.
- Basic dyes are organic dyes that carry a net positive charge. They deposit onto cotton. They are of particular utility for used in composition that contain predominantly cationic surfactants. Dyes may be selected from the basic violet and basic blue dyes listed in the colour index. Preferred examples include triarylmethane basic dyes, methane basic dye, anthraquinone basic dyes, basic blue 16, basic blue 65, basic blue 66, basic blue 67, basic blue 71, basic blue 159, basic violet 19, basic violet 35, basic violet 38, basic violet 48; basic blue 3, basic blue 75, basic blue 95, basic blue 122, basic blue 124, basic blue 141.
- Blue and violet thiazolium mono-azo dyes may also be used as described in WO 2007/084729.
- Reactive dyes are dyes that contain an organic group capable of reacting with cellulose and linking the dye to cellulose with a covalent bond. They deposit onto cotton.
- the reactive group is hydrolysed or the dye has been reacted with an organic species such as a polymer, so - I i
- Dyes may be selected from the reactive violet and reactive blue dyes listed in the colour index. Examples are reactive blue 19, reactive blue 163, reactive blue 182 and reactive blue, reactive blue 96.
- Dye conjugates are formed by binding direct, acid or basic dyes to polymers or particles via physical forces. Dependent on the choice of polymer or particle they deposit on cotton or synthetics. A description is given in WO2006/055787. They may be used as benefit ingredients but are not preferred.
- the benefit ingredient in the film particles comprises 0.01 to lwt% of a photobleach for fabric whiteness and cleaning.
- PB Singlet oxygen photo-bleaches
- the photo-bleach molecule absorbs light and attains an electronical excited state, PB*. This electronically excited state is quenched by triplet oxygen, 3 O 2 , in the surroundings to form singlet 1 O 2 .
- Singlet oxygen is a highly reactive bleach.
- Suitable singlet oxygen photo-bleaches may be selected from, water soluble phthalocyanine compounds, particularly metallated phthalocyanine compounds where the metal is Zn or Al-Zl where Zl is a halide, sulphate, nitrate, carboxylate, alkanolate or hydroxyl ion.
- the phthalocyanine has 1-4 SO3X groups covalently bonded to it where X is an alkali metal or ammonium ion. Such compounds are described in WO2005/014769.
- Xanthene type dyes are preferred, particularly based on the structure :
- the dye may be substituted by halogens and other elements/groups.
- Particularly preferred examples are Food Red 14 and Rose Bengal, Phloxin B, Eosin Y.
- Quantum yields for photosensitized formation of singlet oxygen may be found in J. Phys . Chem.Ref . Data 1993, vol 22, nol ppll3-262. It is preferred if the quantum yield for singlet oxygen formation measured in an organic solvent or D2O is greater than 0.05, more preferably greater than 0.1.
- singlet oxygen producing compounds include chlorophyll, coumarin, porphyrins, myoglobin, riboflavin, bilirubin, and methylene blue.
- the film particles comprise as benefit ingredient 0.01 to 1 wt% of a fluorescent agent (fluorescer), for fabric whiteness.
- a fluorescent agent fluorescer
- Fluorescent agents are well known and many such fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts.
- the total amount of the fluorescent agent or agents used in a laundry detergent composition is from 0.005 to 2 wt %, more preferably 0.01 to 0.1 wt %.
- Preferred fluorescers are: sodium 2 (4-styryl-3-sulfophenyl) -2H-napthol [ 1, 2- d]triazole, disodium 4, 4 ' -bis ⁇ [ (4-anilino-6- (N methyl-N-2 hydroxyethyl) amino 1, 3, 5-triazin-2-yl) ] amino ⁇ stilbeno-2-2 ' disulfonate, disodium 4, 4 ' -bis [ (4-anilino-6-morpholino- 1, 3, 5-triazin-2-yl) amino] stilbene-2-2 ' disulfonate, and disodium 4 , 4 ' -bis (2-sulfostyryl) biphenyl .
- the film particles comprise as benefit ingredient 0.01 to lwt% of an antioxidant, to enhance the lifetime of the fabric.
- a bleach catalyst (other than photobleach) should not be present.
- antioxidants suitable for use in the present invention is alkylated phenols having the general formula:
- R is C1-C22 linear or branched alkyl, preferably methyl or branched C3-C6 alkyl; C3-C6 alkoxy, preferably methoxy; Rl is a C3-C6 branched alkyl, preferably tert- butyl; x is 1 or 2.
- Hindered phenolic compounds are preferred as antioxidant.
- antioxidants suitable for use in the present invention is a benzofuran or benzopyran derivative having the formula:
- Rl and R2 are each independently alkyl or Rl and R2 can be taken together to form a C5-C6 cyclic hydrocarbyl moiety;
- B is absent or CH2 ;
- R4 is C1-C6 alkyl;
- R5 is hydrogen or -C(O)R3 wherein R3 is hydrogen or C1-C19 alkyl;
- R6 is C1-C6 alkyl;
- R7 is hydrogen or C1-C6 alkyl;
- X is - CH2OH, or -CH2A wherein A is a nitrogen comprising unit, phenyl, or substituted phenyl.
- Preferred nitrogen comprising A units include amino, pyrrolidino, piperidino, morpholino, piperazino, and mixtures thereof.
- antioxidants are found as follows. A derivative of ⁇ -tocopherol, beta-tocopherol, gamma- tocopherol, delta-tocopherol, and alkyl esters of gallic acid, especially octyl gallate and dodecyl gallate.
- antioxidants are the class of hindered amine light stabilisers (HALS), particularly those based 2,2,6, 6-tetramethylpipiridines .
- HALS hindered amine light stabilisers
- Non-limiting examples of antioxidants suitable for use in the present invention include phenols inter alia 2,6-di- tert-butylphenol, 2, 6-di-tert-butyl-4-methylphenol, mixtures of 2 and 3- tert-butyl-4-methoxyphenol . Mixtures of antioxidants may be used and in particular mixtures that have synergic antioxidant effects as found in, for example, WO02/072746. Bleach catalyst
- the film particles comprise 0.01 to 1 wt% of a transition metal catalyst, as benefit ingredient, to enhance cleaning of fabric.
- the catalyst is formed from a ligand containing 3 to 5 nitrogen atoms that coordinate to the transition metal.
- Ligands containing pyridine substituents are especially preferred.
- transition metals Fe and Mn are particularly preferred ions.
- the ligand is preferably in the form of a complex of the general formula (Al) :
- M represents a metal selected from Mn(II)-(III)-(IV)- (V), Cu(I)-(II)-(III), Fe(II)-(III)-(IV)-(V), Co(I)-(II)- (III), Ti(II)-(III)-(IV), V(II)-(III)-(IV)-(V), Mo(II)- (IH)-(IV)-(V)-(VI) and W(IV) - (V) - (VI) , preferably selected from Fe (II) - (III) - (IV) - (V) , Mn(II)-(III)-(IV)-(V) or Co(I)- (H)-(III), most preferably Fe (II) - (III) - (IV) - (V) or Mn(II)- (HI)-(IV)-(V); L represents a ligand as herein defined, or its protonated or
- Y in formula (Al) balance the charge z on the complex formed by the ligand L, metal M and coordinating species X.
- Y may be an anion such as RCOO “ , BPh 4 “ , ClO 4 “ , BF 4 “ , PF 6 “ , RSO 3 “ , RSO 4 “ , SO 4 2” , NO 3 “ , F “ , Cl “ , Br “ , or I “ , with R being hydrogen, optionally substituted alkyl or optionally substituted aryl.
- Y may be a common cation such as an alkali metal, alkaline earth metal or (alkyl) ammonium cation.
- Suitable counter ions Y include those that give rise to the formation of storage-stable solids.
- Preferred counter ions for the preferred metal complexes are selected from R 7 COO “ , ClO 4 " , BF 4 “ , PF 6 “ , RSO 3 “ (in particular CF 3 SO 3 “ ), RSO 4 “ , SO 4 2” , NO 3 “ , F “ , Cl “ , Br “ , and I “ , wherein R represents hydrogen or optionally substituted phenyl, naphthyl or Ci-C 4 alkyl.
- Ligands of the form are preferred.
- Rl to R4 may be the same or different and are H, and linear or branched, substituted or unsubstituted C1-C20 alkyl, alkylaryl, alkenyl or alkynyl.
- opposite R groups may together form a bridge, preferably an ethylene bridge, and
- Ligands may be substituted as appropriate. For example they may be substituted by sulphonic and carboxylic acid groups; amines; quaternary amines; alkyl and alkoxy groups such as methyl, methoxy, ethyl and ethoxy; halogens; CN; and NO2.
- a preferred ligand is of the form:
- R 1 is independently selected from H, and linear or branched, substituted or unsubstituted C1-C20 alkyl, alkylaryl, alkenyl or alkynyl.
- R 1 is methyl, most preferably ethyl.
- a preferred ligand is of the form:
- -NR6R7 is selected from the group consisting of -
- the ethylene bridge carrying the tertiary nitrogen is substituted by an alkyl group, preferably a methyl group. Most preferably the alkyl group is alpha to the bicyclo nitrogen carrying tertiary nitrogen.
- a film containing the [nitrolotris (2, 1-ethanediyloxy) ] tris [propanol] salt of direct violet 9 was prepared as follows :
- the resulting film is taken from the glass plate and cut into the desired film particle shapes.
- the solution had an optical absorption at 550 nm (lcm path length) of 0.875.
- the film particle is calculated to contain 13 times more dye per weight than the granules .
- the powder contained 18 wt% sodium LAS, 73 wt% salts (silicate, sodium tripolyphosphate, sodium sulphate, sodium carbonate) , remainder impurities water and minors (enzymes and fluorescer) .
- the three samples were labelled A, B and C.
- To A was added 0.100g of the carbonate granule of Example 2.
- To B was added O.Ollg of the dye benefit ingredient containing film particles of Example 1.
- To C was added 0.084g of the film particles of Example 1.
- the amounts of shading dye benefit ingredient in the samples were in the ratio A:B:C of 1:1.4:11.
- Example B and C the dye film was cut into film particles with a cross sectional area of 5 to 6 mm 2 .
- a 1.7g piece of bleached non-mercerised, white woven cotton sheeting was placed in a beaker, so that the fabric filled the bottom of the beaker in a single flat layer. To this was added 100ml of demineralised water, then sample A was sprinkled over the cloth. The solution was gently agitated for a minute then left for 5 minutes. The cloth was removed and thoroughly rinsed twice, and left to dry.
- the petal is a film particle with cross-sectional area of 10 to 20 mm 2 and a film composition consisting of primary alkyl sulphate surfactant and polyvinyl alcohol polymer.
- the quantity given in this line includes the minor quantities of benefit ingredients included in the film particle and identified separately by "(petal)".
- NI (7EO) refers to R- (OCH 2 CH 2 ) n 0H, where R is an alkyl chain of C12 to C15, and n is 7.
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)
- Biochemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08804761.8A EP2195410B1 (en) | 2007-10-12 | 2008-09-25 | Performance ingredients in film particles |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2037MU2007 | 2007-10-12 | ||
EP08150103 | 2008-01-08 | ||
PCT/EP2008/062876 WO2009047128A1 (en) | 2007-10-12 | 2008-09-25 | Performance ingredients in film particles |
EP08804761.8A EP2195410B1 (en) | 2007-10-12 | 2008-09-25 | Performance ingredients in film particles |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2195410A1 true EP2195410A1 (en) | 2010-06-16 |
EP2195410B1 EP2195410B1 (en) | 2016-07-20 |
Family
ID=40090417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08804761.8A Not-in-force EP2195410B1 (en) | 2007-10-12 | 2008-09-25 | Performance ingredients in film particles |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP2195410B1 (en) |
CN (1) | CN101878291A (en) |
AR (1) | AR068860A1 (en) |
BR (1) | BRPI0818084A2 (en) |
CL (1) | CL2008003020A1 (en) |
ES (1) | ES2598487T3 (en) |
WO (1) | WO2009047128A1 (en) |
ZA (1) | ZA201001429B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019144371A1 (en) * | 2018-01-26 | 2019-08-01 | The Procter & Gamble Company | Unitary laundry detergent article |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2012012096A (en) | 2010-04-26 | 2012-12-17 | Novozymes As | Enzyme granules. |
BR112013009698B1 (en) * | 2010-10-22 | 2020-04-28 | Milliken & Co | composed of bluing agents |
US8378083B2 (en) | 2010-10-22 | 2013-02-19 | Milliken & Company | Bis-azo colorants for use as bluing agents |
CN107475235B (en) | 2011-06-20 | 2022-09-13 | 诺维信公司 | Particulate composition |
WO2012175708A2 (en) | 2011-06-24 | 2012-12-27 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
CN112662734B (en) | 2011-06-30 | 2024-09-10 | 诺维信公司 | Method for screening alpha-amylase |
CN103797104A (en) | 2011-07-12 | 2014-05-14 | 诺维信公司 | Storage-stable enzyme granules |
WO2013024021A1 (en) | 2011-08-15 | 2013-02-21 | Novozymes A/S | Polypeptides having cellulase activity and polynucleotides encoding same |
WO2013041689A1 (en) | 2011-09-22 | 2013-03-28 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
US20140342433A1 (en) | 2011-11-25 | 2014-11-20 | Novozymes A/S | Subtilase Variants and Polynucleotides Encoding Same |
US20140335596A1 (en) | 2011-12-20 | 2014-11-13 | Novozymes A/S | Subtilase Variants and Polynucleotides Encoding Same |
AU2013213601B8 (en) | 2012-01-26 | 2018-01-18 | Novozymes A/S | Use of polypeptides having protease activity in animal feed and detergents |
EP2814956B1 (en) | 2012-02-17 | 2017-05-10 | Novozymes A/S | Subtilisin variants and polynucleotides encoding same |
WO2013131964A1 (en) | 2012-03-07 | 2013-09-12 | Novozymes A/S | Detergent composition and substitution of optical brighteners in detergent compositions |
AR090971A1 (en) | 2012-05-07 | 2014-12-17 | Novozymes As | POLYPEPTIDES THAT HAVE XANTANE DEGRADATION ACTIVITY AND POLYCINOCYLODES THAT CODE THEM |
US20150140165A1 (en) | 2012-06-20 | 2015-05-21 | Novozymes A/S | Use of polypeptides having protease activity in animal feed and detergents |
US9551042B2 (en) | 2012-12-21 | 2017-01-24 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
US9902946B2 (en) | 2013-01-03 | 2018-02-27 | Novozymes A/S | Alpha-amylase variants and polynucleotides encoding same |
WO2014183921A1 (en) | 2013-05-17 | 2014-11-20 | Novozymes A/S | Polypeptides having alpha amylase activity |
CN114634921B (en) | 2013-06-06 | 2024-09-10 | 诺维信公司 | Alpha-amylase variants and polynucleotides encoding same |
EP3013955A1 (en) | 2013-06-27 | 2016-05-04 | Novozymes A/S | Subtilase variants and polynucleotides encoding same |
US10378001B2 (en) | 2013-06-27 | 2019-08-13 | Novozymes A/S | Subtilase variants and compositions comprising same |
US20160152925A1 (en) | 2013-07-04 | 2016-06-02 | Novozymes A/S | Polypeptides Having Anti-Redeposition Effect and Polynucleotides Encoding Same |
EP3339436B1 (en) | 2013-07-29 | 2021-03-31 | Henkel AG & Co. KGaA | Detergent composition comprising protease variants |
RU2670946C9 (en) | 2013-07-29 | 2018-11-26 | Новозимс А/С | Protease variants and polynucleotides encoding them |
WO2015014803A1 (en) | 2013-07-29 | 2015-02-05 | Novozymes A/S | Protease variants and polynucleotides encoding same |
WO2015049370A1 (en) | 2013-10-03 | 2015-04-09 | Novozymes A/S | Detergent composition and use of detergent composition |
US10030239B2 (en) | 2013-12-20 | 2018-07-24 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
US20160348035A1 (en) | 2014-03-05 | 2016-12-01 | Novozymes A/S | Compositions and Methods for Improving Properties of Non-Cellulosic Textile Materials with Xyloglucan Endotransglycosylase |
US20160333292A1 (en) | 2014-03-05 | 2016-11-17 | Novozymes A/S | Compositions and Methods for Improving Properties of Cellulosic Textile Materials with Xyloglucan Endotransglycosylase |
EP3126479A1 (en) | 2014-04-01 | 2017-02-08 | Novozymes A/S | Polypeptides having alpha amylase activity |
US20170121695A1 (en) | 2014-06-12 | 2017-05-04 | Novozymes A/S | Alpha-amylase variants and polynucleotides encoding same |
EP3739029A1 (en) | 2014-07-04 | 2020-11-18 | Novozymes A/S | Subtilase variants and polynucleotides encoding same |
EP3878960A1 (en) | 2014-07-04 | 2021-09-15 | Novozymes A/S | Subtilase variants and polynucleotides encoding same |
CN107075489A (en) | 2014-11-20 | 2017-08-18 | 诺维信公司 | Alicyclic acid bacillus variant and the polynucleotides for encoding them |
CN107075493B (en) | 2014-12-04 | 2020-09-01 | 诺维信公司 | Subtilase variants and polynucleotides encoding same |
EP3234121A1 (en) | 2014-12-15 | 2017-10-25 | Henkel AG & Co. KGaA | Detergent composition comprising subtilase variants |
EP3310912B1 (en) | 2015-06-18 | 2021-01-27 | Novozymes A/S | Subtilase variants and polynucleotides encoding same |
EP3106508B1 (en) | 2015-06-18 | 2019-11-20 | Henkel AG & Co. KGaA | Detergent composition comprising subtilase variants |
CN108291215A (en) | 2015-10-14 | 2018-07-17 | 诺维信公司 | Polypeptide with proteinase activity and encode their polynucleotides |
US10479981B2 (en) | 2015-10-14 | 2019-11-19 | Novozymes A/S | DNase variants |
CN109715792A (en) | 2016-06-03 | 2019-05-03 | 诺维信公司 | Subtilase variants and the polynucleotides that it is encoded |
WO2018011276A1 (en) | 2016-07-13 | 2018-01-18 | The Procter & Gamble Company | Bacillus cibi dnase variants and uses thereof |
EP3476936B1 (en) | 2017-10-27 | 2022-02-09 | The Procter & Gamble Company | Detergent compositions comprising polypeptide variants |
EP3701017A1 (en) | 2017-10-27 | 2020-09-02 | Novozymes A/S | Dnase variants |
WO2019201793A1 (en) | 2018-04-17 | 2019-10-24 | Novozymes A/S | Polypeptides comprising carbohydrate binding activity in detergent compositions and their use in reducing wrinkles in textile or fabric. |
BR112021018731A2 (en) | 2019-03-21 | 2021-12-21 | Novozymes As | Alpha-amylase variants and polynucleotides encoding them |
WO2020207944A1 (en) | 2019-04-10 | 2020-10-15 | Novozymes A/S | Polypeptide variants |
WO2021037895A1 (en) | 2019-08-27 | 2021-03-04 | Novozymes A/S | Detergent composition |
WO2021053127A1 (en) | 2019-09-19 | 2021-03-25 | Novozymes A/S | Detergent composition |
EP4038170A1 (en) | 2019-10-03 | 2022-08-10 | Novozymes A/S | Polypeptides comprising at least two carbohydrate binding domains |
EP3892708A1 (en) | 2020-04-06 | 2021-10-13 | Henkel AG & Co. KGaA | Cleaning compositions comprising dispersin variants |
EP4225905A2 (en) | 2020-10-07 | 2023-08-16 | Novozymes A/S | Alpha-amylase variants |
EP4291646A2 (en) | 2021-02-12 | 2023-12-20 | Novozymes A/S | Alpha-amylase variants |
WO2022268885A1 (en) | 2021-06-23 | 2022-12-29 | Novozymes A/S | Alpha-amylase polypeptides |
WO2024131880A2 (en) | 2022-12-23 | 2024-06-27 | Novozymes A/S | Detergent composition comprising catalase and amylase |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2374082A (en) * | 2001-04-04 | 2002-10-09 | Procter & Gamble | Particles for a detergent product |
DE10360842A1 (en) | 2003-12-20 | 2004-12-16 | Henkel Kgaa | Dye-containing shaped body with delayed dye release, e.g. useful in detergents, comprises a water-soluble thermoplastic polymer, an ionic salt, an at least bi-ionic dye and a particulate acarrier |
WO2007130684A1 (en) | 2006-05-05 | 2007-11-15 | The Procter & Gamble Company | Films with microcapsules |
DE102008026584A1 (en) | 2008-06-03 | 2009-12-10 | Clariant International Limited | Improved cyan colorant |
-
2008
- 2008-09-25 ES ES08804761.8T patent/ES2598487T3/en active Active
- 2008-09-25 BR BRPI0818084A patent/BRPI0818084A2/en not_active Application Discontinuation
- 2008-09-25 WO PCT/EP2008/062876 patent/WO2009047128A1/en active Application Filing
- 2008-09-25 EP EP08804761.8A patent/EP2195410B1/en not_active Not-in-force
- 2008-09-25 CN CN2008801117706A patent/CN101878291A/en active Pending
- 2008-10-10 CL CL2008003020A patent/CL2008003020A1/en unknown
- 2008-10-14 AR ARP080104470A patent/AR068860A1/en unknown
-
2010
- 2010-02-26 ZA ZA2010/01429A patent/ZA201001429B/en unknown
Non-Patent Citations (1)
Title |
---|
See references of WO2009047128A1 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019144371A1 (en) * | 2018-01-26 | 2019-08-01 | The Procter & Gamble Company | Unitary laundry detergent article |
CN111511887A (en) * | 2018-01-26 | 2020-08-07 | 宝洁公司 | Integrated laundry detergent article |
CN111511887B (en) * | 2018-01-26 | 2022-04-08 | 宝洁公司 | Integrated laundry detergent article |
Also Published As
Publication number | Publication date |
---|---|
AR068860A1 (en) | 2009-12-09 |
CL2008003020A1 (en) | 2009-06-05 |
EP2195410B1 (en) | 2016-07-20 |
ZA201001429B (en) | 2011-05-25 |
CN101878291A (en) | 2010-11-03 |
ES2598487T3 (en) | 2017-01-27 |
BRPI0818084A2 (en) | 2017-07-04 |
WO2009047128A1 (en) | 2009-04-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2009047128A1 (en) | Performance ingredients in film particles | |
EP2201092A1 (en) | Granular detergent compositions with contrasting lamellar visual cues | |
ES2413054T3 (en) | Incorporation of dye in granular laundry composition | |
CA2569559C (en) | Laundry detergent compositions with efficient hueing dye | |
ES2372328T3 (en) | COMPOSITION OF MATIZED. | |
EP2300589B1 (en) | Shading composition | |
CN102985521B (en) | Compositions comprising optical benefit agents | |
US7208459B2 (en) | Laundry detergent compositions with efficient hueing dye | |
EP1902122A1 (en) | Dye delivery granules | |
AU2011315791A1 (en) | Laundry detergent particles | |
WO2012048947A1 (en) | Laundry detergent particles | |
EP2316915B1 (en) | Fabric treatment composition with a fabric substantive dye | |
ES2368976T3 (en) | DARK COMPOSITION. | |
US20070203052A1 (en) | Laundry Composition | |
EP3775121B1 (en) | Dye granule | |
EP2721135B1 (en) | Incorporation of dye into granular laundry composition | |
EP2441822A1 (en) | Laundry detergent particles | |
EP2331670B1 (en) | Cationic isothiazolium dyes |
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: 20100224 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA MK RS |
|
RAX | Requested extension states of the european patent have changed |
Extension state: BA Payment date: 20100224 |
|
17Q | First examination report despatched |
Effective date: 20150821 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C11D 3/37 20060101ALI20160310BHEP Ipc: C11D 17/02 20060101ALI20160310BHEP Ipc: C11D 3/39 20060101ALI20160310BHEP Ipc: C11D 17/04 20060101ALI20160310BHEP Ipc: C11D 3/42 20060101ALI20160310BHEP Ipc: C11D 17/06 20060101AFI20160310BHEP Ipc: C11D 3/40 20060101ALI20160310BHEP |
|
INTG | Intention to grant announced |
Effective date: 20160404 |
|
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): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
DAX | Request for extension of the european patent (deleted) | ||
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 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 814129 Country of ref document: AT Kind code of ref document: T Effective date: 20160815 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602008045218 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: RO Ref legal event code: EPE |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 9 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20160720 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 814129 Country of ref document: AT Kind code of ref document: T Effective date: 20160720 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2598487 Country of ref document: ES Kind code of ref document: T3 Effective date: 20170127 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20160720 Ref country code: IT 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: 20160720 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: 20160720 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: 20160720 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: 20161120 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: 20161020 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: 20160720 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160720 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: 20160720 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: 20161021 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: 20161121 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: 20160720 Ref country code: PL 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: 20160720 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: 20160720 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R026 Ref document number: 602008045218 Country of ref document: DE |
|
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: 20160720 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: 20160720 |
|
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
26 | Opposition filed |
Opponent name: HENKEL AG & CO. KGAA Effective date: 20170420 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20160720 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: 20160720 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: 20161020 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: 20160720 |
|
PLAX | Notice of opposition and request to file observation + time limit sent |
Free format text: ORIGINAL CODE: EPIDOSNOBS2 |
|
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: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160930 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160930 Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160925 |
|
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: 20160925 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: 20160720 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 10 |
|
PLBB | Reply of patent proprietor to notice(s) of opposition received |
Free format text: ORIGINAL CODE: EPIDOSNOBS3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20080925 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: 20160720 |
|
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 NON-PAYMENT OF DUE FEES Effective date: 20160930 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 11 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R100 Ref document number: 602008045218 Country of ref document: DE |
|
PLCK | Communication despatched that opposition was rejected |
Free format text: ORIGINAL CODE: EPIDOSNREJ1 |
|
PLBN | Opposition rejected |
Free format text: ORIGINAL CODE: 0009273 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: OPPOSITION REJECTED |
|
27O | Opposition rejected |
Effective date: 20181017 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20190927 Year of fee payment: 12 Ref country code: RO Payment date: 20190824 Year of fee payment: 12 Ref country code: DE Payment date: 20190918 Year of fee payment: 12 Ref country code: TR Payment date: 20190919 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20190925 Year of fee payment: 12 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20191022 Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602008045218 Country of ref document: DE |
|
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 NON-PAYMENT OF DUE FEES Effective date: 20200925 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20200925 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20210401 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200925 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20220119 |
|
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: 20200926 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200925 |