EP2556140A1 - Optimized release of bleaching systems in laundry detergents - Google Patents
Optimized release of bleaching systems in laundry detergentsInfo
- Publication number
- EP2556140A1 EP2556140A1 EP11715128A EP11715128A EP2556140A1 EP 2556140 A1 EP2556140 A1 EP 2556140A1 EP 11715128 A EP11715128 A EP 11715128A EP 11715128 A EP11715128 A EP 11715128A EP 2556140 A1 EP2556140 A1 EP 2556140A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- unit dose
- laundry detergent
- weight
- dose laundry
- peroxygen source
- 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.)
- Ceased
Links
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- 238000004061 bleaching Methods 0.000 title claims abstract description 23
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- 239000011148 porous material Substances 0.000 description 1
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
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- AJTVWPGZWVJMEA-UHFFFAOYSA-N ruthenium tungsten Chemical compound [Ru].[Ru].[W].[W].[W] AJTVWPGZWVJMEA-UHFFFAOYSA-N 0.000 description 1
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
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- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
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- 150000005846 sugar alcohols Polymers 0.000 description 1
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- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
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- 235000010493 xanthan gum Nutrition 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/3917—Nitrogen-containing compounds
- C11D3/392—Heterocyclic compounds, e.g. cyclic imides or lactames
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
- C11D17/043—Liquid or thixotropic (gel) compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
- C11D17/045—Multi-compartment
Definitions
- the present invention relates to stable, convenient to use, unit dose laundry detergent articles that are capable of delivering good cleaning, including bleaching, while also being safe for fabrics.
- Peroxygen sources such as hydrogen peroxide, with or without bleach activators, are used for removing stains, and improving the whiteness of light coloured fabrics during laundry. However, such agents tend to have lower efficacy at colder temperatures.
- a means to achieve better low temperature bleaching performance is through the use of organic bleach catalysts in combination with activated peroxygen sources. To maximize the bleaching efficiency, it is desirable to rapidly and uniformly distribute the bleach catalyst, and preferably the activated peroxygen source, into the wash. In addition, by rapidly and uniformly distributing the bleach catalyst and activated peroxygen source, fabric damage due to spot bleaching is avoided.
- a means to achieve this is to incorporate a bleaching system, comprising organic bleach catalysts and activated peroxygen sources, into a liquid laundry detergent composition.
- the present invention provides for a unit dose laundry detergent article comprising: an anionic and/or nonionic surfactant; and a bleaching system comprising: an organic bleach catalyst consisting of an aryliminium ion selected from the group: cations, zwitterions, and mixtures thereof; and an activated peroxygen source selected from the group consisting of: a preformed peracid; a hydrogen peroxide source; and mixtures thereof; enclosed in a water-soluble or dispersible film, wherein: at least 50 % by weight of the anionic and/or nonionic surfactant, and at least 50 % by weight of the aryliminium ions are comprised in at least one fluid composition.
- unit dose laundry detergent article refers to any laundry treatment composition in single usage form.
- the unit dose laundry detergent article of the invention comprises at least one "fluid comprising compartment” and may optionally comprise a solid component. If present, the solid component may be in a separate compartment, suspended in a fluid-filled compartment, or as part of a paste.
- a fluid-filled compartment refers to a partition of the unit dose laundry detergent article comprising a fluid capable of wetting a fabric e.g., clothing.
- the term, fluid includes such forms as liquids, gels and pastes.
- the fluid contained in the fluid comprising compartment may include solids or gases in suitably subdivided form, but excludes forms which are non-fluid overall, such as tablets or granules.
- Unit dose laundry detergent articles of the present invention comprise, in single, easy to use dosage form: an anionic and/or nonionic surfactant, an aryliminium ion, and an activated peroxygen source.
- Such unit dose articles have the benefit of ensuring that the correct dosages of the bleaching ingredients are delivered.
- the amount of the aryliminium ion and the activated peroxygen source, as well as their ratio, is preferably carefully controlled.
- the unit dose laundry detergent article preferably also comprises anionic nonsoap surfactants; other surfactants, especially additional nonionic surfactants; non-aminofunctional organic solvents, and laundering adjuncts for improved cleaning and fabric care.
- the unit dose laundry detergent article comprises one or more compartments.
- a multicompartment unit dose form may be desirable for such reasons as: separating chemically incompatible ingredients; or where it is desirable for a portion of the ingredients to be released into the wash earlier or later.
- Detergent compositions of the present invention comprise, preferably from 1% to 70%, more preferably from 10% to 50%, and most preferably from 15% o 45% by weight of an anionic and/or nonionic surfactant.
- the unit dose laundry detergent articles of the present invention preferably comprise from 1 to 70 %, more preferably from 5 to 50 % by weight of one or more anionic surfactants.
- Preferred anionic surfactant are selected from the group consisting of: C11-C18 alkyl benzene sulfonates, C10-C20 branched-chain and random alkyl sulfates, C10-C18 alkyl ethoxy sulfates, mid-chain branched alkyl sulfates, mid-chain branched alkyl alkoxy sulfates, C10-C18 alkyl alkoxy carboxylates comprising 1-5 ethoxy units, modified alkylbenzene sulfonate, C12- C20 methyl ester sulfonate, C10-C18 alpha-olefin sulfonate, C6-C20 sulfosuccinates, and mixtures thereof.
- compositions of the present invention preferably comprise at least one sulphonic acid surfactant, such as a linear alkyl benzene sulphonic acid, or the water-soluble salt forms.
- Anionic sulfonate or sulfonic acid surfactants suitable for use herein include the acid and salt forms of linear or branched C5-C20, more preferably C10-C16, most preferably C11-C13 alkylbenzene sulfonates, C5-C20 alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C5-C20 sulfonated polycarboxylic acids, and mixtures thereof.
- the aforementioned surfactants can vary widely in their 2-phenyl isomer content.
- Anionic sulphate salts suitable for use in compositions of the invention include: primary and secondary alkyl sulphates, having a linear or branched alkyl or alkenyl moiety having from 9 to 22 carbon atoms, more preferably from 12 tol8 carbon atoms; beta-branched alkyl sulphate surfactants; and mixtures thereof.
- Mid- chain branched alkyl sulphates or sulfonates are also suitable anionic surfactants for use in the compositions of the invention.
- Preferred are the C5-C22, preferably C10-C20 mid-chain branched alkyl primary sulphates.
- a suitable average total number of carbon atoms for the alkyl moieties is preferably within the range of from 14.5 to 17.5.
- Preferred mono-methyl -branched primary alkyl sulphates are selected from the group consisting of the 3- methyl to 13-methyl pentadecanol sulphates, the corresponding hexadecanol sulphates, and mixtures thereof. Dimethyl derivatives or other biodegradable alkyl sulphates having light branching can similarly be used.
- Other suitable anionic surfactants for use herein include fatty methyl ester sulphonates and/or alkyl ethyoxy sulphates (AES) and/or alkyl polyalkoxylated carboxylates (AEC). Mixtures of anionic surfactants can be used, for example mixtures of alkylbenzenesulphonates and AES.
- the anionic surfactants are typically present in the form of their salts with alkanolamines or alkali metals such as sodium and potassium.
- the anionic surfactants are neutralized with alkanolamines, such as monoethanolamine or triethanolamine, and are fully soluble in the fluid phase.
- Nonionic surfactants The unit dose laundry detergent articles of the present invention may include from 1 to 70 %, preferably from 5 to 50 % by weight of a nonionic surfactant.
- Suitable nonionic surfactants include, but are not limited to C12-C18 alkyl ethoxylates ("AE") including the so-called narrow peaked alkyl ethoxylates, C6-C12 alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxy/propoxy), block alkylene oxide condensate of C6-C12 alkyl phenols, alkylene oxide condensates of C8-C22 alkanols and ethylene oxide/propylene oxide block polymers (PluronicO-BASF Corp.), as well as semi polar nonionics (e.g., amine oxides and phosphine oxides).
- AE alkyl ethoxylates
- AE alkyl ethoxylates
- Alkylpolysaccharides such as disclosed in U.S. Pat. 4,565,647 are also useful nonionic surfactants for compositions of the invention.
- alkyl polyglucoside surfactants are also useful nonionic surfactants for compositions of the invention.
- suitable nonionic surfactants include those of the formula Rl(OC 2 H 4 ) n OH, wherein Rl is a C10-C16 alkyl group or a C8-C12 alkyl phenyl group, and n is from 3 to 80.
- the nonionic surfactants may be condensation products of C12-C15 alcohols with from 5 to 20 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with about 6.5 moles of ethylene oxide per mole of alcohol.
- Additional suitable nonionic surfactants include polyhydroxy fatty acid amides of the formula:
- R is a C9-C17 alkyl or alkenyl
- Rl is a methyl group
- Z is glycidyl derived from a reduced sugar or alkoxylated derivative thereof. Examples are N-methyl N-l-deoxyglucityl cocoamide and N-methyl N-l-deoxyglucityl oleamide.
- the unit dose laundry detergent article comprises an organic bleach catalyst and an activated peroxygen source.
- organic bleach catalysts improve the bleaching performance, particularly at low temperatures. They are capable of accepting an oxygen atom from an activated peroxygen source and transferring the oxygen atom to an oxidizable substrate.
- the organic bleach catalyst of the present invention comprises an aryliminium ion.
- the aryliminium ions may be cations, zwitterions, or a mixture thereof.
- at least 50%, preferably at least 80%, more preferably 100%, by weight of the aryliminium ions are comprised in the fluid comprising compartment of the unit dose laundry detergent article.
- the unit dose laundry detergent article may comprise from 0.001% to 10%, preferably from 0.01% to 5%, more preferably from 0.1% to 2% by weight percent of the aryliminium ion.
- the unit dose laundry detergent article may comprise from 0.1% to 30%, preferably from 0.5% to 20%, more preferably from 1% to 10% by weight percent of the activated peroxygen source.
- the aryliminium ions of the present invention react with activated peroxygen sources such as peracids to form aryloxaziridinium ions, which bleach oxidizable substrates.
- the unit dose laundry detergent article preferably comprises a weight ratio of the aryliminium ion to activated peroxygen source of from 2:1 to 1:500, preferably from 1:1 to 1:100, more preferably from 1:5 to 1:50, still more preferably from 1:10 to 1:30.
- the stability of the aryliminium ions (and resultant aryloxaziridinium ions) is affected by the wash temperature at dilutions typically found in the wash liquor. At lower wash temperatures, such as from 5 °C to 30 °C, the decomposition rate of the organic bleach catalyst is reduced, compared to at higher wash temperatures, such as above 40 °C. In contrast, typical bleaching agents, such as peroxides with or without bleach activators, are less effective at reduced wash temperatures. Therefore, aryliminium ions are particularly useful for improving the efficacy of bleaching systems for low temperature laundry applications.
- the bleaching system for use in the present invention may also include other bleaching agents such as: bleach activators, metal-containing bleach catalysts, transition metal complexes of macropolycyclic rigid ligands, and mixtures thereof.
- Suitable aryliminium zwitterions maybe selected from the group consisting of:
- R 1 is selected from the group consisting of: H, a branched alkyl group containing from 3 to 24 carbons, and a linear alkyl group containing from 1 to 24 carbons.
- R is a branched alkyl group comprising from 6 to 18 carbons, or a linear alkyl group comprising from 5 to 18 carbons, more preferably each R 1 is selected from the group consisting of: 2-propylheptyl, 2-butyloctyl, 2-pentylnonyl, 2-hexyldecyl, n-hexyl, n-octyl, n-decyl, n- dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl, iso-nonyl, iso-decyl, iso-tridecyl and iso- pentadecyl; R 2 is independently selected from the group consisting of: H, a branched alkyl group comprising from 3 to 12 carbons, and a linear alkyl group comprising from 1 to 12 carbons.
- Preferabl R 2 is independently selected from H
- R 1 is a branched alkyl group containing from 9 to 24 carbons or linear alkyl group containing from 11 to 24 carbons, preferably, each R 1 is a branched alkyl group containing from 9 to 18 carbons or linear alkyl group containing from 11 to 18 carbons, more preferably each R 1 is selected from the group consisting of 2-propylheptyl, 2-butyloctyl, 2-pentylnonyl, 2- hexyldecyl, n-dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl, iso-nonyl, iso-decyl, iso-tridecyl and iso-pentadecyl.
- Suitable aryliminium zwitterions include those listed in Table la, Table lb, and mixtures thereof.
- Preferred aryliminium zwitterions are those listed in Table lb, and mixtures thereof.
- Most preferred, are the inner salts of 3-(3,4-dihydroisoquinolinium) propane sulfonate, sulphuric acid mono-[2-(3,4-dihydro-isoquinolin-2-yl)-l-(2-butyl-octyloxymethyl)-ethyl] ester, and mixtures thereof.
- Other suitable examples of organic bleach catalysts can be found in US 5,576,282 and US 5,817,614, EP 923,636 Bl, WO 2001/16263 Al, WO 2000/42156 Al, WO 2007/001262 Al.
- Suitable cations and polycations include aryliminium ions
- R 3 is independently selected from the group consisting of: H and methyl groups.
- R 3 is H.
- R 4 and R 5 are independently selected from the group consisting of: H, a branched alkyl group containing from 3 to 12 carbons, and a linear alkyl group containing from 1 to 12 carbons.
- R 4 and R 5 are H or methyl, more preferably, R 4 and R 5 are H.
- X is a charge-balancing counterion; preferably a bleach-compatible counterion. Suitable aryliminium cations include those listed in Table 2, and mixtures thereof.
- N-methyl-3,4- dihydroisoquinolinium tetrafluoroborate N- methyl-3,4-dihydroisoquinolinium p-toluene sulphonate, and mixtures thereof.
- the stability of the aryliminium ion is improved when the fluid comprising compartment that contains the aryliminuim ion has a neat pH of less than 9, preferably less than 8.5, more preferably less than 8, even more preferably less than 7.
- the pH of the fluid comprising compartment that contains the aryliminuim ion is from 5 to 7.
- Activated peroxygen sources supply the oxygen atoms that are transferred to the oxidizeable substrate and as such, are an essential feature of the bleaching system.
- the activated peroxygen source is selected from the group consisting of: a preformed peracid, a hydrogen peroxide source, and mixtures thereof.
- the activated peroxygen source is preferably at least partially physically separated from the aryliminium ions, such that the activated peroxygen source and organic bleach catalyst are unable to interact chemically.
- at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source is a solid.
- catalyzed degradation of the peroxygen source by the aryliminium ions is inhibited by the solid-liquid phase boundary.
- at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source is encapsulated by a water-soluble or dispersible barrier which keeps the majority of the activated peroxygen source isolated from the aryliminium ions.
- Suitable water-soluble or dispersible barrier materials include carbohydrates, natural or synthetic gums, chitin and chitosan, cellulose and cellulose derivatives, polyvinyl alcohol and polyvinyl alcohol derivatives, polyvinyl acetate, polyethylene glycol, synthetic and natural waxes, gelatin, alginates, acrylic polymers and their derivatives, starch materials, an inorganic coating (silicates, phosphates, carbonates, zeolites, alumina and mixtures thereof), urea-formaldehyde, melamine-formaldehyde, fatty acids, polyurethanes, polyamides, polyureas, polyesters and mixtures thereof.
- At least 50%, preferably at least 80%, more preferably 100%, by weight of the activated peroxygen source is in a different compartment comprising less than 25%, preferable less than 10%, more preferably, less than 1 %, by weight of the aryliminium ions.
- the activated peroxygen source can be physically separated from ingredients such as enzymes and perfumes that are sensitive to bleaching agents.
- Such embodiments include unit dose laundry detergent articles, further comprising a detersive enzyme selected from the group consisting of: lipase, protease, amylase, cellulase, pectate lyase, xyloglucanase, and mixtures thereof; wherein at least part of the activated peroxygen source is physically separated from the detersive enzyme by a means selected from the group consisting of: at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being a solid; at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being encapsulated by a water-soluble or dispersible barrier; and at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being in a different compartment comprising less than 25%, preferable less than 10%, more preferably
- the unit dose laundry detergent articles further comprising a perfume; wherein at least part of the activated peroxygen source is physically separated from the perfume by a means selected from the group consisting of: at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being a solid; at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being encapsulated by a water-soluble or dispersible barrier; and at least 50%, preferably 80%, more preferably 100%, by weight of the activated peroxygen source being in a different compartment comprising less than 25%, preferable less than 10%, more preferably, less than 1%, by weight of the perfume.
- Suitable preformed peracids include, but are not limited to, compounds selected from the group consisting of: phthalimido peroxycaproic acid (PAP), percarboxylic acids and salts, percarbonic acids and salts, perimidic acids and salts, peroxymonosulphuric acids and salts, and mixtures thereof. Phthalimido peroxycaproic acid (PAP) is preferred.
- a suitable salt of a peroxymonosulphuric acid is potassium peroxymonosulphate (potassium monopersulphate), or its triple salt: 2KHSO5.KHSO4.K2SO4.
- the stability of fluid comprising compartments containing a preformed peracid is improved by having a neat pH of from 4 to 10, preferably from 6.5 to 9, more preferably from 7 to 8.5.
- peracids such as phthalimido peroxycaproic acid are less prone to ring-opening in such a pH range. It is believed that more of the peracid is protonated in this pH range, resulting in slower availability of the peracid. This gives more time for the organic bleach booster to distribute over the substrate, leading to improved stain bleaching.
- the preformed peracid may be present at a level of from 0.1% to 30%, preferably from 0.5% to 25%, more preferably from 1% to 10%, most preferably from 2% to 4% by weight of the encapsulated portion of the unit dose laundry detergent article.
- an even higher level of peracid may be present for unit dose laundry detergent articles for use primarily as a bleach additive.
- such compositions may comprise from 10% to 40%, preferably from 15% to 30%, more preferably from 15% to 25%, by weight preformed peracid.
- at least 80% by weight of the preformed peracid is encapsulated in a compartment comprising less than 25% by weight of the aryliminium ions.
- Hydrogen peroxide sources include: peroxides, persalts, and mixtures thereof. Embodiments of the invention may comprise from 0.1% to 30%, preferably from 0.5% to 20%, more preferably from 1% to 10% by weight of a hydrogen peroxide source. Hydrogen peroxide is one of the most powerful oxidizers known. It is a very selective bleaching agent causing less textile fibre damage compared to many other peroxygen sources and tends to be less aggressive on fabric dyes, detergent enzymes and optical brighteners. When incorporated into unit dose laundry detergent articles of the invention, add-on levels of 0.1% to 10%, preferably 0.5 to 5%, by weight of hydrogen peroxide are preferred.
- Suitable peroxides also include organic peroxides, such as diacyl peroxides, that do not cause visible spotting or filming.
- organic peroxides such as diacyl peroxides
- dibenzoyl peroxide is one example.
- suitable hydrogen peroxide sources are described in detail in Kirk Othmer's Encyclopaedia of Chemical Technology, 4th Ed (1992, John Wiley & Sons), Vol. 4, pp. 271-300 "Bleaching Agents (Survey)".
- Suitable persalts include: percarbonates, perborates, persulphates, perphosphates, persilicates. Percarbonates and perborates are preferred. Percarbonates are particularly preferred for their greater rate of dissolution, a more environmentally friendly profile and the advantage of concurrently generating hydrogen peroxide, while also liberating carbonate. Thus, they give a higher pH than perborates and favour perhydrolysis. Sodium percarbonate is a suitable percarbonate.
- Perborate sources such as sodium perborate, have good stability and selectivity. Other preferred perborate sources include the tetrahydrate and/or the monohydrate. For improved stability, the persalt may be coated.
- the bleaching system of the present invention can be formulated with a bleach activator in combination with a persalt and/or peroxide.
- Persalts particularly percarbonates and/or perborates, are preferred.
- An example of a suitable peroxide is dibenzoyl peroxide.
- the bleach activator is preferably selected from the group consisting of: nonanoyloxybenzene sulphonate (NOBS), sodium 4-(isononanoyloxy)benzenesulphonate (iso-NOBS), tetraacetyl ethylene diamine (TAED) or mixtures thereof.
- NOBS nonanoyloxybenzene sulphonate
- iso-NOBS sodium 4-(isononanoyloxy)benzenesulphonate
- TAED tetraacetyl ethylene diamine
- DAP diacyl peroxide
- bleach activators may be selected from the group consisting of: benzoylcaprolactam (BzCL), 4-nitrobenzoylcaprolactam, 3-chlorobenzoyl-icaprolactam, benzoyloxybenzenesulphonate (BOBS), phenyl benzoate (PhBz), decanoyloxybenzenesulphonate (CIO-OBS), benzoylvalerolactam (BZVL), octanoyloxybenzenesulphonate (C8-OBS), perhydrolyzable esters and mixtures thereof, alternatively benzoylcaprolactam and benzoylvalerolactam, 4-[N-(nonaoyl) amino hexanoyloxy] -benzene sulfonate sodium salt (NACA-OBS) (See U.S.
- LOBS dodecanoyloxy-benzenesulphonate
- UOBS 10-undecenoyloxybenzenesulfonate
- DOBA decanoyloxybenzoic acid
- suitable bleach activators including quaternary substituted bleach activators, are described in US 6,855,680.
- the aryliminium ion may be selected to incorporate bleach activation properties.
- Preferred bleach catalysts include manganese and cobalt- containing bleach catalysts.
- Other suitable metal-containing bleach catalysts include catalyst systems comprising a transition metal cation of defined bleach catalytic activity, such as copper, iron, titanium, ruthenium tungsten, molybdenum, or manganese cations; an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminium cations; and a sequestrate having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra (methylenephosphonic acid) and water- soluble salts thereof.
- Suitable catalyst systems are disclosed in US 4,430,243.
- the unit dose laundry detergent articles herein may also include bleach catalysts comprising a transition metal complex, preferably of a macropolycyclic rigid ligand.
- the amount used is preferably from 0.0001% to 5%, more preferably from 0.001% to 2%, most preferably from 0.01% to 1% by weight of the encapsulated portion of the unit dose laundry detergent article.
- the unit dose laundry detergent article of the present invention may also include conventional laundry detergent ingredients selected from the group consisting of: additional surfactants, non- aminofunctional organic solvents, enzymes, enzyme stabilizers, amphiphilic alkoxylated grease cleaning polymers, clay soil cleaning polymers, soil release polymers, soil suspending polymers, bleaching systems, optical brighteners, hueing dyes, particulate material, perfume and other odour control agents, hydrotropes, suds suppressors, fabric care benefit agents, pH adjusting agents, dye transfer inhibiting agents, preservatives, non-fabric substantive dyes and mixtures thereof.
- additional surfactants selected from the group consisting of: additional surfactants, non- aminofunctional organic solvents, enzymes, enzyme stabilizers, amphiphilic alkoxylated grease cleaning polymers, clay soil cleaning polymers, soil release polymers, soil suspending polymers, bleaching systems, optical brighteners, hueing dyes, particulate material, perfume and other odour control agents, hydrotropes, suds suppressor
- the unit dose laundry detergent articles of the present invention may comprise additional surfactant selected from the group consisting: anionic, cationic, nonionic, amphoteric and/or zwitterionic surfactants and mixtures thereof.
- Suitable cationic surfactants can be water-soluble, water-dispersible or water-insoluble. Such cationic surfactants have at least one quaternized nitrogen and at least one long-chain hydrocarbyl group. Compounds comprising two, three or even four long-chain hydrocarbyl groups are also included. Examples include alkyltrimethylammonium salts, such as C12 alkyltrimethylammonium chloride, or their hydroxyalkyl substituted analogues. The present invention may comprise 1% or more of cationic surfactants.
- Amphoteric detersive surfactants suitable for use in the composition include those surfactants broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight or branched chain and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulphonate, sulphate, phosphate, or phosphonate.
- Suitable amphoteric detersive surfactants for use in the present invention include, but are not limited to: cocoamphoacetate, cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixtures thereof.
- Zwitterionic detersive surfactants suitable for use in unit dose laundry detergent articles are well known in the art, and include those surfactants broadly described as derivatives of aliphatic quaternary ammonium, phosphonium, and sulphonium compounds, in which the aliphatic radicals can be straight or branched chain, and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulfonate, sulphate, phosphate or phosphonate. Zwitterionics such as betaines are also suitable for this invention.
- amine oxide surfactants having the formula: R(EO)x(PO)y(BO) z N(0)(CH 2 R') 2 -qH20 are also useful in compositions of the present invention.
- R is a relatively long-chain hydrocarbyl moiety which can be saturated or unsaturated, linear or branched, and can contain from 8 to 20, preferably from 10 to 16 carbon atoms, and is more preferably C12-C16 primary alkyl.
- R' is a short-chain moiety preferably selected from hydrogen, methyl and -CH 2 OH.
- EO is ethyleneoxy
- PO propyleneneoxy
- BO butyleneoxy.
- Amine oxide surfactants are illustrated by C12-C14 alkyldimethyl amine oxide.
- Non-limiting examples of other anionic, zwitterionic, amphoteric or optional additional surfactants suitable for use in the compositions are described in McCutcheon's, Emulsifiers and Detergents, 1989 Annual, published by M. C. Publishing Co., and U.S. Pat. Nos. 3,929,678, 2,658,072; 2,438,091 ; 2,528,378.
- the fluid comprising compartments of the unit dose laundry detergent article preferably comprise less than 20%, more preferably less than 15%, most preferably less than 10% by weight water.
- the fluid comprising compartment may be almost entirely non-aqueous, preferably comprising from 2% to 40 %, more preferably from 5 to 25 % by weight of a non-aminofunctional organic solvent.
- Such fluid comprising compartments may comprise very little water, for instance, that which is introduced with other raw materials.
- non-aminofunctional organic solvent refers to any organic solvent which contains no amino functional groups.
- Preferred non-aminofunctional organic solvents include monohydric alcohols, dihydric alcohols, polyhydric alcohols, glycerol, glycols, polyalkylene glycols such as polyethylene glycol, and mixtures thereof. Highly preferred are mixtures of solvents, especially mixtures of two or more of the following: lower aliphatic alcohols such as ethanol, propanol, butanol, isopropanol; diols such as 1,2-propanediol or 1,3 -propanediol; and glycerol.
- embodiments of unit dose laundry detergent articles of the present invention may include embodiments in which propanediols are used but methanol and ethanol are not used.
- non-aminofunctional organic solvents are liquid at ambient temperature and pressure (i.e. 21°C and 1 atmosphere), and comprise carbon, hydrogen and oxygen.
- Non-aminofunctional organic solvents may be present when preparing a premix of the external structuring system, or in the final unit dose laundry detergent article.
- the unit dose laundry detergent articles of the present invention may comprise from 0.0001 % to 8 % by weight of a detersive enzyme which provides cleaning performance and/or fabric care benefits.
- a detersive enzyme which provides cleaning performance and/or fabric care benefits.
- Such compositions preferably have a composition pH of from 6 to 10.5.
- Suitable enzymes can be selected from the group consisting of: lipase, protease, amylase, cellulase, pectate lyase, xyloglucanase, and mixtures thereof.
- a preferred enzyme combination comprises a cocktail of conventional detersive enzymes such as lipase, protease, cellulase and amylase. Detersive enzymes are described in greater detail in U.S. Patent No. 6,579,839.
- Enzyme Stabilizers Enzymes can be stabilized using any known stabilizer system such as calcium and/or magnesium compounds, boron compounds and substituted boric acids, aromatic borate esters, peptides and peptide derivatives, polyols, low molecular weight carboxylates, relatively hydrophobic organic compounds [e.g.
- esters dialkyl glycol ethers, alcohols or alcohol alkoxylates], alkyl ether carboxylate in addition to a calcium ion source, benzamidine hypochlorite, lower aliphatic alcohols and carboxylic acids, N,N-bis(carboxymethyl) serine salts; (meth) acrylic acid- (meth) acrylic acid ester copolymer and PEG; lignin compound, polyamide oligomer, glycolic acid or its salts; poly hexamethylene biguanide or N,N-bis-3-amino-propyl- dodecyl amine or salt; and mixtures thereof.
- the unit dose laundry detergent article comprises from 0.1% to 7%, more preferably from 0.2% to 3%, of a polymer deposition aid.
- polymer deposition aid refers to any cationic polymer or combination of cationic polymers that significantly enhance deposition of a fabric care benefit agent onto the fabric during laundering.
- Suitable polymer deposition aids can comprise a cationic polysaccharide and/or a copolymer.
- Fabric care benefit agent refers to any material that can provide fabric care benefits.
- Non-limiting examples of fabric care benefits include, but are not limited to: fabric softening, colour protection, colour restoration, pill/fuzz reduction, anti-abrasion and anti- wrinkling.
- fabric care benefit agents include: silicone derivatives, oily sugar derivatives, dispersible polyolefins, polymer latexes, cationic surfactants and combinations thereof.
- the unit dose laundry detergent articles herein may optionally contain from 0.01 to 20% by weight of one or more cleaning polymers that provide for broad-range soil cleaning of surfaces and fabrics and/or suspension of the soils. Any suitable cleaning polymer may be of use.
- Useful cleaning polymers are described in US 2009/0124528A1. Non-limiting examples of useful categories of cleaning polymers include: amphiphilic alkoxylated grease cleaning polymers; clay soil cleaning polymers; soil release polymers; and soil suspending polymers.
- Optical brighteners These are also known as fluorescent whitenening agents for textiles. Preferred levels are from 0.001% to 2% by weight of the encapsulated portion of the unit dose laundry detergent article. Suitable brighteners are disclosed in EP 68669 IB and include hydrophobic as well as hydrophilic types. Brightener 49 is preferred for use in the present invention.
- Hueing dyes or fabric shading dyes are useful laundering adjuncts in unit dose laundry detergent articles. Suitable dyes include blue and/or violet dyes having a hueing or shading effects. See, for example, WO 2009/087524 Al, WO2009/087034A1 and references therein. Recent developments that are suitable for the present invention include sulfonated phthalocyanine dyes having a zinc or aluminium central atom.
- the unit dose laundry detergent articles herein may comprise from 0.00003% to 0.1%, preferably from 0.00008% to 0.05% by weight of the fabric hueing dye.
- the unit dose laundry detergent article may include particulate material such as clays, suds suppressors, encapsulated oxidation- sensitive and/or thermally sensitive ingredients such as perfumes (perfume microcapsules), bleaches and enzymes; or aesthetic adjuncts such as pearlescent agents including mica, pigment particles, or the like. Suitable levels are from 0.0001% to 10%, or from 0.1% to 5% by weight of the encapsulated portion of the unit dose laundry detergent article.
- the unit dose laundry detergent article comprises a free and/or micro-encapsulated perfume. If present, the free perfume is typically incorporated at a level from 0.001 to 10%, preferably from 0.01% to 5%, more preferably from 0.1% to 3% by weight of the encapsulated portion of the unit dose laundry detergent article.
- the perfume raw materials can be protected from oxidation by the bleach system.
- the perfume microcapsule is formed by at least partially surrounding the perfume raw materials with a wall material.
- the microcapsule wall material comprises: melamine crosslinked with formaldehyde, polyurea, urea crosslinked with formaldehyde or urea crosslinked with gluteraldehyde.
- Suitable perfume microcapsules and perfume nanocapsules include those described in the following references: US 2003215417 Al ; US 2003216488 Al ; US 2003158344 Al ; US 2003165692 Al; US 2004071742 Al ; US 2004071746 Al ; US 2004072719 Al; US 2004072720 Al ; EP 1393706 Al ; US 2003203829 Al ; US 2003195133 Al; US 2004087477 Al ; US 20040106536 Al ; US 6645479; US 6200949; US 4882220; US 4917920; US 4514461 ; US RE 32713; US 4234627.
- the unit dose laundry detergent article comprises odour control agents such as uncomplexed cyclodextrin, as described in US 5,942,217.
- odour control agents such as uncomplexed cyclodextrin, as described in US 5,942,217.
- suitable odour control agents include those described in: US 5,968,404, US 5,955,093, US 6,106,738, US 5,942,217, and US 6,033,679.
- the encapsulated portion of the unit dose laundry detergent article typically comprises a hydrotrope in an effective amount, preferably up to 15%, more preferably from 1 % to 10 %, most preferably from 3 % o 6 % by weight, so that the fluid laundry detergent compositions are compatible in water.
- Suitable hydrotropes for use herein include anionic-type hydrotropes, particularly sodium, potassium, and ammonium xylene sulfonate, sodium, potassium and ammonium toluene sulfonate, sodium potassium and ammonium cumene sulfonate, and mixtures thereof, as disclosed in US 3,915,903.
- External structuring system is a compound or mixture of compounds which provide either a sufficient yield stress or low shear viscosity to stabilize the fluid independently from, or extrinsic from, the structuring effect of any detersive surfactants in the composition.
- the fluid within any compartment of the present invention may comprise from 0.01% to 5%, preferably from 0.1% to 1% by weight of an external structuring system.
- Suitable external structuring systems include non-polymeric crystalline, hydroxy-functional structurants, polymeric structurants, or mixtures thereof.
- the external structurant system imparts a high shear viscosity at 20 s "1 at 21°C of from 1 to 1500 cps, and a viscosity at low shear (0.05 s "1 at 21°C) of greater than 5000 cps.
- the viscosity is measured using an AR 550 rheometer from TA instruments using a plate steel spindle at 40 mm diameter and a gap size of 500 ⁇ .
- the high shear viscosity at 20s "1 and low shear viscosity at 0.5s " can be obtained from a logarithmic shear rate sweep from 0.1s "1 to 25s "1 in 5 minutes time at 21°C.
- the external structuring system may comprise from 0.01 to 1% by weight of a non-polymeric crystalline, hydroxyl functional structurant.
- a non-polymeric crystalline, hydroxyl functional structurant generally comprise a crystallisable glyceride which can be pre-emulsified to aid dispersion into the final unit dose laundry detergent article.
- Preferred crystallisable glycerides include hydrogenated castor oil or "HCO" or derivatives thereof, provided that it is capable of crystallizing in the fluid detergent composition.
- suitable external structuring systems may comprise from 0.01 to 5% by weight of a naturally derived and/or synthetic polymeric structurant.
- Suitable naturally derived polymeric structurants include: hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose, polysaccharide derivatives and mixtures thereof.
- Suitable polysaccharide derivatives include: pectine, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, xanthan gum, guar gum and mixtures thereof.
- suitable synthetic polymeric structurants include: polycarboxylates, polyacrylates, hydrophobically modified ethoxylated urethanes, hydrophobically modified non-ionic polyols and mixtures thereof.
- Unit dose pouch material
- the contents of the unit-dose compartments can generally be prepared by mixing the ingredients together.
- the contents of the unit-dose compartments are enclosed in a water-soluble or dispersible film.
- the water-soluble or dispersible film preferably has a water- solubility of at least 50%, more preferably at least 75% or even at least 95%.
- the water-solubility is measured by the method set out here: 5.0 grams ⁇ 0.1 gram of the water-soluble or dispersible film 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 sintered-glass filter with a pore size of maximum 20 microns.
- 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 dispersibility can be calculated.
- Preferred polymers, copolymers or derivatives thereof suitable for use as water-soluble or dispersible films are selected from: polyvinyl pyrrolidone, polyalkylene oxides, acrylamide, acrylic acid, cellulose, cellulose ethers, cellulose esters, cellulose amides, polyvinyl acetates, polycarboxylic acids and salts, polyaminoacids or peptides, polyamides, polyacrylamide, copolymers of maleic/acrylic acids, polysaccharides including starch and gelatine, natural gums such as xanthan and carragum.
- More preferred polymers are selected from polyacrylates and water-soluble acrylate copolymers, methylcellulose, carboxymethylcellulose sodium, dextrin, ethylcellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, maltodextrin, polymethacrylates, and most preferred are: polyvinyl alcohols, polyvinyl alcohol copolymers, hydroxypropyl methyl cellulose (HPMC), and combinations thereof.
- HPMC hydroxypropyl methyl cellulose
- films comprising polyvinyl alcohol, polyvinyl alcohol copolymers, or mixtures thereof, makes them especially preferred for use in the present invention. Such films dissolve particularly swiftly, such that the aryliminium ions are able to distribute rapidly and uniformly throughout the wash.
- 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.
- Example la and lb Single compartment unit-dose laundry detergent articles of the present invention, encapsulated in a polyvinyl alcohol film.
- Example 2a and 2b Single compartment unit-dose laundry detergent articles of the present invention, encapsulated in a polyvinyl alcohol film.
- Example 3a, 3b and 3c Dual compartment unit-dose laundry detergent articles of the present invention, encapsulated in a polyvinyl alcohol film, wherein the activated peroxygen source is in a separate compartment from the other laundry ingredients.
- Example 5a and 5b Dual compartment unit-dose laundry detergent articles of the present invention, encapsulated in a polyvinyl alcohol film, wherein the activated peroxygen source and the organic catalyst are in separate compartments.
- Amylase and protease Example 6 A 3 -compartment unit-dose laundry detergent article of the present invention, encapsulated in a polyvinyl alcohol film, wherein the activated peroxygen source, the organic catalyst, and the enzymes, are in separate compartments.
- Examples 7a and 7b Dual compartment unit-dose laundry detergent articles of the present invention, encapsulated in a polyvinyl alcohol film, wherein the activated peroxygen source is separated from the other active ingredients.
- the stability of the aryliminium ion at different pH was evaluated by adjusting the pH of the composition of Example la to a pH of 7, 8, and 9 (using either HCl or NaOH), and measuring the percentage of the aryliminium ion remaining after storage for two weeks at 21°C and also 32°C: Organic Bleach Catalyst Stability (% Remaining) at 2 weeks pH Storage temp (°C) % Aryliminium ion remaining
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Abstract
Description
Claims
Applications Claiming Priority (2)
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US32125810P | 2010-04-06 | 2010-04-06 | |
PCT/US2011/031312 WO2011127102A1 (en) | 2010-04-06 | 2011-04-06 | Optimized release of bleaching systems in laundry detergents |
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EP2556140A1 true EP2556140A1 (en) | 2013-02-13 |
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EP11715128A Ceased EP2556140A1 (en) | 2010-04-06 | 2011-04-06 | Optimized release of bleaching systems in laundry detergents |
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US (1) | US20110240510A1 (en) |
EP (1) | EP2556140A1 (en) |
JP (1) | JP5863767B2 (en) |
CN (1) | CN102869760A (en) |
AR (1) | AR080838A1 (en) |
BR (1) | BR112012025395A2 (en) |
CA (1) | CA2795176C (en) |
MX (1) | MX2012011514A (en) |
RU (1) | RU2569297C2 (en) |
WO (1) | WO2011127102A1 (en) |
ZA (1) | ZA201207401B (en) |
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- 2011-04-06 MX MX2012011514A patent/MX2012011514A/en unknown
- 2011-04-06 AR ARP110101155A patent/AR080838A1/en not_active Application Discontinuation
- 2011-04-06 BR BR112012025395A patent/BR112012025395A2/en not_active IP Right Cessation
- 2011-04-06 RU RU2012142725/04A patent/RU2569297C2/en not_active IP Right Cessation
- 2011-04-06 JP JP2013503863A patent/JP5863767B2/en not_active Expired - Fee Related
- 2011-04-06 EP EP11715128A patent/EP2556140A1/en not_active Ceased
- 2011-04-06 CA CA2795176A patent/CA2795176C/en not_active Expired - Fee Related
- 2011-04-06 WO PCT/US2011/031312 patent/WO2011127102A1/en active Application Filing
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2012
- 2012-10-03 ZA ZA2012/07401A patent/ZA201207401B/en unknown
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Also Published As
Publication number | Publication date |
---|---|
AR080838A1 (en) | 2012-05-09 |
MX2012011514A (en) | 2012-11-06 |
BR112012025395A2 (en) | 2016-06-28 |
ZA201207401B (en) | 2013-12-23 |
CN102869760A (en) | 2013-01-09 |
CA2795176C (en) | 2015-05-26 |
JP5863767B2 (en) | 2016-02-17 |
RU2012142725A (en) | 2014-05-20 |
CA2795176A1 (en) | 2011-10-13 |
RU2569297C2 (en) | 2015-11-20 |
US20110240510A1 (en) | 2011-10-06 |
WO2011127102A1 (en) | 2011-10-13 |
WO2011127102A4 (en) | 2011-12-01 |
JP2013523976A (en) | 2013-06-17 |
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