WO2020016194A1 - Particules de distribution d'agent bénéfique - Google Patents

Particules de distribution d'agent bénéfique Download PDF

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Publication number
WO2020016194A1
WO2020016194A1 PCT/EP2019/069044 EP2019069044W WO2020016194A1 WO 2020016194 A1 WO2020016194 A1 WO 2020016194A1 EP 2019069044 W EP2019069044 W EP 2019069044W WO 2020016194 A1 WO2020016194 A1 WO 2020016194A1
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WO
WIPO (PCT)
Prior art keywords
benefit agent
shell
methyl
particles
oil
Prior art date
Application number
PCT/EP2019/069044
Other languages
English (en)
Inventor
Craig Warren Jones
Andrew Philip Parker
Original Assignee
Unilever Plc
Unilever N.V.
Conopco, Inc., D/B/A Unilever
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Plc, Unilever N.V., Conopco, Inc., D/B/A Unilever filed Critical Unilever Plc
Priority to CN201980047653.6A priority Critical patent/CN112567013B/zh
Priority to EP19737568.6A priority patent/EP3824061B1/fr
Priority to BR112021000737-7A priority patent/BR112021000737B1/pt
Publication of WO2020016194A1 publication Critical patent/WO2020016194A1/fr
Priority to ZA2021/00030A priority patent/ZA202100030B/en

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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
    • C11D3/50—Perfumes
    • C11D3/502—Protected perfumes
    • C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
    • 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
    • C11D1/38—Cationic compounds
    • C11D1/65—Mixtures of anionic with cationic 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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
    • 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
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29—Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/38—Cationic compounds
    • C11D1/62—Quaternary ammonium compounds

Definitions

  • the present invention relates to benefit agent (such as fragrance) delivery particles and compositions (such as laundry treatment compositions) comprising them.
  • benefit agent such as fragrance
  • compositions such as laundry treatment compositions
  • the fragrance experienced by consumers is one of the most important attributes. Efficient delivery of the right fragrances to the fabric during the laundry process and release of that fragrance at key consumer moments is critical to the delivery of clean and fresh laundry.
  • fragrance at key moments is a difficult task since laundry detergents are usually designed to carry oily materials or particulate solids away from the laundered fabric. Fragrances, however, are also typically oily materials.
  • Encapsulation of fragrance allows for improved deposition of fragrance to fabric, as well as delaying the release of fragrance when the consumer garment is being worn.
  • the invention provides a benefit agent delivery particle having a core-shell structure in which a porous shell of polymeric material entraps a core containing the benefit agent; in which the pores in the shell are at least partially occluded by a wash-removable coating provided at the exterior surface of the shell; and characterized in that the wash-removable coating is formed from deposited particles of a complex of a cationic surfactant and an anionic surfactant.
  • the invention also provides a laundry treatment composition comprising a benefit agent delivery particle as defined above.
  • the core of the benefit agent delivery particle of the invention is typically formed in an inner region of the particle and provides a sink for the benefit agent.
  • the shell generally protects the benefit agent from the external environment and regulates the flow of benefit agent into and out of the core.
  • the presence of the wash-removable coating serves to reduce the leakage of the entrapped benefit agent through the pores in the shell. Removal of the coating during a washing operation facilitates release of the entrapped benefit agent.
  • washing operation generally denotes a method of laundering fabric using a laundry treatment composition according to the invention.
  • the wash-removable coating is formed from deposited particles of a complex of a cationic surfactant and an anionic surfactant.
  • the complex has a solubility in distilled water (at 25°C and at atmospheric pressure) of less than about 10mg/L, preferably less than about 1 mg/L, to prevent the coating being removed too quickly in the wash.
  • the cationic surfactant is first mixed with an aqueous slurry of pre-formed particles having a core-shell structure in which a porous shell of polymeric material surrounds a core containing the benefit agent (hereinafter termed“pre-formed core-shell particles”).
  • pre-formed core-shell particles a core-shell structure in which a porous shell of polymeric material surrounds a core containing the benefit agent
  • the cationic surfactant deposits onto the exterior surface of the shell of the pre-formed core- shell particles.
  • the anionic surfactant is then added to the mixture of particles so that it forms a complex with the deposited cationic surfactant on the exterior shell surface of the particles.
  • the charged heads of the respective surfactants are neutralized during complexation.
  • Anionic surfactants and cationic surfactants for use in the formation of the complex generally have molecular weights of about 1000 or below and solubilities in distilled water (at 25°C and at atmospheric pressure) of at least about 10mg/L, preferably at least about 100mg/L.
  • Suitable cationic surfactants for use in the formation of the complex may be selected from mono-long chain quaternary ammonium compounds of the general formula (I):
  • R 1 is selected from linear or branched alkyl or alkenyl chains containing from 6 to 24 carbon atoms and 0 or 1 double bond
  • R 2 ,R 3 and R 4 are each independently selected from C1 to C3 alkyl groups and -(C n H2 n O) x H groups in which n is 2 or 3 and x is from 1 to about 3)
  • X is an anion selected from chloride, bromide, iodide, nitrate, sulfate, methylsulfate, ethylsulfate, acetate and phosphate.
  • R 1 is selected from C16 to C22 linear saturated alkyl chains and R 2 , R 3 and R 4 are each independently selected from CH3 and CH2CH2OH, more preferably CH3.
  • Suitable cationic surfactants for use in the formation of the complex include cetyltrimethylammonium chloride (CTAC), stearyltri methyl ammonium chloride (STAC), behenyltrimethylammonium chloride (BTAC) and mixtures thereof.
  • Suitable anionic surfactants for use in the formation of the complex may be selected from salts of organic sulfates and sulfonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term“alkyl” being used to include the alkyl portion of higher acyl radicals.
  • alkyl sulfates examples include alkyl sulfates, alkyl ether sulfates, alkaryl sulfonates, alpha-olefin sulfonates and mixtures thereof.
  • the alkyl radicals preferably contain from 10 to 18 carbon atoms and may be unsaturated.
  • the alkyl ether sulfates may contain from one to ten ethylene oxide or propylene oxide units per molecule, and preferably contain one to three ethylene oxide units per molecule.
  • the counterion for anionic surfactants is generally an alkali metal such as sodium or potassium; or an ammoniacal counterion such as monoethanolamine, (MEA)
  • DEA diethanolamine
  • TAA triethanolamine
  • Preferred anionic surfactants for use in the formation of the complex include
  • alkylbenzene sulfonates particularly linear alkylbenzene sulfonates (LAS) with an alkyl chain length of from 10 to 18 carbon atoms.
  • LAS is a mixture of closely related isomers and homologues alkyl chain homologues, each containing an aromatic ring sulfonated at the“para” position and attached to a linear alkyl chain at any position except the terminal carbons.
  • the linear alkyl chain typically has a chain length of from 1 1 to 15 carbon atoms, with the predominant materials having a chain length of about C12.
  • Each alkyl chain homologue consists of a mixture of all the possible sulfophenyl isomers except for the 1 -phenyl isomer.
  • alkyl ether sulfates having a straight or branched chain alkyl group having 10 to 18, more preferably 12 to 14 carbon atoms and containing an average of 1 to 3EO units per molecule.
  • a preferred example is sodium lauryl ether sulfate (SLES) in which the predominantly C12 lauryl alkyl group has been ethoxylated with an average of 3EO units per molecule.
  • Preferred pre-formed core-shell particles have a negative charge at their exterior shell surface and have a zeta potential of from -0.1 meV to -100meV, more preferably from - 10meV to -80 meV, and most preferably from - 20meV to -75meV.
  • the zeta potential is suitably measured by a dynamic light scattering (DLS) method using a Zetasizer NanoTM ZS90 (Malvern Instruments Ltd, UK) at 25° C.
  • a dispersion of the particles in deionised water with a solids content of around 500 ppm and a pH adjusted to about 7 is used for the measurement.
  • Pre-formed core-shell particles may suitably be made using methods known to those skilled in the art such as coacervation, interfacial polymerization, and polycondensation.
  • Coacervation typically involves encapsulation of a generally water- insoluble core material by the precipitation of colloidal material(s) onto the surface of droplets of the material.
  • Coacervation may be simple e.g. using one colloid such as gelatin, or complex where two or possibly more colloids of opposite charge, such as gelatin and gum arabic or gelatin and carboxymethyl cellulose, are used under carefully controlled conditions of pH, temperature and concentration.
  • Interfacial polymerisation typically proceeds with the formation of a fine dispersion of oil droplets (the oil droplets containing the core material) in an aqueous continuous phase.
  • the dispersed droplets form the core of the future core-shell particle and the dimensions of the dispersed droplets directly determine the size of the future core-shell particle.
  • Shell- forming materials are contained in both the dispersed phase (oil droplets) and the aqueous continuous phase and they react together at the phase interface to build a polymeric wall around the oil droplets thereby to encapsulate the droplets.
  • An example of a core-shell particle produced by this method has a polyurea shell formed by reaction of diisocyanates or polyisocyanates with diamines or
  • Polycondensation involves forming a dispersion or emulsion of the core material in an aqueous solution of precondensate of polymeric materials under appropriate conditions of agitation to produce dispersed core material of a desired particle size, and adjusting the reaction conditions to cause condensation of the precondensate by acid catalysis, resulting in the condensate separating from solution and surrounding the dispersed core material to produce a coherent film and the desired particles.
  • An example of a core-shell particle produced by this method has an aminoplast shell formed from the
  • polycondensation product of melamine (2,4,6-triamino-1 ,3,5-triazine) or urea with formaldehyde e.g. melamine (2,4,6-triamino-1 ,3,5-triazine) or urea with formaldehyde.
  • Suitable cross-linking agents e.g. toluene diisocyanate, divinyl benzene, butanediol diacrylate
  • secondary wall polymers may also be used as appropriate, e.g. anhydrides and their derivatives, particularly polymers and co- polymers of maleic anhydride.
  • the porous shell of polymeric material is preferably an aminoplast shell formed from the polycondensation product of melamine with formaldehyde.
  • the shell is preferably of a generally spherical shape; and will typically comprise at most 20% by weight based on the total weight of the benefit agent delivery particle.
  • the benefit agent delivery particle of the invention will generally have an average particle size between 100 nanometers and 50 microns. Particles larger than this are entering the visible range. Examples of particles in the sub-micron range include latexes and mini- emulsions with an average particle size ranging from 100 to 600 nanometers.
  • Core-shell particles suitable for use in the invention preferably have an average size of from 0.6 to 50 microns, more preferably from 2 to 30 microns and most preferably from 5 to 25 microns.
  • the particle size distribution can be narrow, broad or multimodal. If necessary, the particles as initially produced may be filtered or screened to produce a product of greater size uniformity.
  • Size refers to diameter unless otherwise stated.
  • diameter means the z-average particle size measured, for example, using dynamic light scattering (as set out in international standard ISO 13321 ) with an instrument such as a Zetasizer NanoTM
  • diameter means the apparent volume median diameter (D50), measurable for example, by laser diffraction (as set out in international standard ISO 13320) with an instrument such as a MastersizerTM 2000 (Malvern Instruments Ltd, UK).
  • the benefit agent delivery particle of the invention may be provided with a deposition aid at the exterior shell surface.
  • Deposition aids serve to modify the properties of the exterior shell surface, for example to make the particle more substantive to a desired substrate.
  • Desired substrates include cellulosics (including cotton) and polyesters (including those employed in the manufacture of polyester fabrics).
  • the deposition aid may suitably be provided at the exterior shell surface by means of covalent bonding, entanglement or strong adsorption.
  • a deposition aid is attached to the exterior shell surface by means of covalent bonding, either directly or via a linking species.
  • Deposition aids for use in the invention may suitably be selected from polysaccharides having an affinity for cellulose.
  • polysaccharides may be naturally occurring or synthetic and may have an intrinsic affinity for cellulose or may have been derivatised or otherwise modified to have an affinity for cellulose.
  • Suitable polysaccharides have a 1-4 linked b glycan (generalised sugar) backbone structure with at least 4, and preferably at least 10 backbone residues which are b1-4 linked, such as a glucan backbone (consisting of b1-4 linked glucose residues), a mannan backbone (consisting of b1-4 linked mannose residues) or a xylan backbone (consisting of b1 -4 linked xylose residues).
  • Examples of such b1 -4 linked polysaccharides include xyloglucans, glucomannans, mannans, galactomannans, b(1-3),(1-4) glucan and the xylan family incorporating glucurono-, arabino- and glucuronoarabinoxylans.
  • Preferred b1 -4 linked polysaccharides for use in the invention may be selected from xyloglucans of plant origin, such as pea xyloglucan and tamarind seed xyloglucan (TXG) (which has a b1 -4 linked glucan backbone with side chains of a-D xylopyranose and b-D-galactopyranosyl-(1-2)-a-D-xylo-pyranose, both 1-6 linked to the backbone); and galactomannans of plant origin such as locust bean gum (LBG) (which has a mannan backbone of b1 -4 linked mannose residues, with single unit galactose side chains linked a1-6 to the backbone).
  • xyloglucans of plant origin such as pea xyloglucan and tamarind seed xyloglucan (TXG) (which has a b1 -4 linked glucan backbone with side chains of a-D
  • polysaccharides which may gain an affinity for cellulose upon hydrolysis, such as cellulose mono-acetate; or modified polysaccharides with an affinity for cellulose such as hydroxypropyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl
  • methylcellulose hydroxypropyl guar, hydroxyethyl ethylcellulose and methylcellulose.
  • Deposition aids for use in the invention may also be selected from phthalate containing polymers having an affinity for polyester.
  • phthalate containing polymers may have one or more nonionic hydrophilic segments comprising oxyalkylene groups (such as oxyethylene, polyoxyethylene, oxypropylene or polyoxypropylene groups), and one or more hydrophobic segments comprising terephthalate groups.
  • the oxyalkylene groups will have a degree of polymerization of from 1 to about 400, preferably from 100 to about 350, more preferably from 200 to about 300.
  • a suitable example of a phthalate containing polymer of this type is a copolymer having random blocks of ethylene terephthalate and polyethylene oxide terephthalate.
  • Deposition aids for use in the invention will generally have a weight average molecular weight (M w ) in the range of from about 5 kDa to about 500 kDa, preferably from
  • the core contains a benefit agent.
  • Preferred benefit agents in the context of fabric laundering include fragrance formulations, clays, enzymes, antifoams, fluorescers, bleaching agents and precursors thereof
  • conditioning agents for example cationic surfactants including water-insoluble quaternary ammonium materials, fatty alcohols and/or silicones
  • lubricants e.g. sugar polyesters
  • colour and photo-protective agents including sunscreens
  • antioxidants e.g. ceramides
  • reducing agents e.g. sodium sulfate
  • sequestrants e.g. sodium sulfate
  • colour care additives including dye fixing agents
  • unsaturated oil emollients, moisturizers, insect repellents and/or pheromones
  • drape modifiers e.g. polymer latex particles such as PVAc
  • antimicrobial or microbe control agents e.g. polymer latex particles such as PVAc
  • fragrance formulations are fragrance formulations.
  • Fragrance formulations for use in the invention will typically contain a blend of selected fragrant components, optionally mixed with one or more excipients.
  • the combined odours of the various fragrant components produce a pleasant or desired fragrance.
  • the term“fragrant component” in the context of this invention denotes a material which is used essentially for its ability to impart a pleasant odour to a composition (into which it is incorporated), and/or a surface (to which it is applied), either on its own or in admixture with other such materials. Materials having these characteristics are generally small, lipophilic molecules of sufficient volatility to be transported to the olfactory system in the upper part of the nose.
  • Fragrant components for use in the invention will typically have molecular weights of less than 325 atomic mass units, preferably less than 300 atomic mass units and more preferably less than 275 atomic mass units.
  • the molecular weight is preferably greater than 100 atomic mass units and more preferably greater than 125 atomic mass units, since lower masses may be too volatile and/or insufficiently lipophilic to be effective.
  • Fragrant components for use in the invention will preferably have a molecular structure which does not contain halogen atoms and/or strongly ionizing functional groups such as sulfonates, sulfates, or quaternary ammonium ions.
  • Fragrant components for use in the invention will more preferably have a molecular structure containing only atoms from among, but not necessarily all, of the following: hydrogen, carbon, oxygen, nitrogen and sulphur. Most preferably the fragrant components will have a molecular structure containing only atoms from among, but not necessarily all, of the following: hydrogen, carbon and oxygen.
  • fragrant components include aromatic, aliphatic and araliphatic
  • hydrocarbons having molecular weights from about 90 to about 250; aromatic, aliphatic and araliphatic esters having molecular weights from about 130 to about 250; aromatic, aliphatic and araliphatic nitriles having molecular weights from about 90 to about 250; aromatic, aliphatic and araliphatic alcohols having molecular weights from about 90 to about 240; aromatic, aliphatic and araliphatic ketones having molecular weights from about 150 to about 270; aromatic, aliphatic and araliphatic lactones having molecular weights from about 130 to about 290; aromatic, aliphatic and araliphatic aldehydes having molecular weights from about 90 to about 230; aromatic, aliphatic and araliphatic ethers having molecular weights from about 150 to about 270; and condensation products of aldehydes and amines having molecular weights from about 180 to about 320.
  • cyclic and cycloaliphatic alcohols such as, for example, 4-tert-butylcyclohexanol, 3,3,5-trimethylcyclohexanol, 3-isocamphylcyclohexanol, 2,6,9-trimethyl-Z2,Z5,E9- cyclododecatrien-1-ol, 2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, alpha, 3,3- trimethylcyclo-hexylmethanol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopent-1 -yl)butanol, 2- methyl-4-(2,2,3-trimethyl-3-cyclopent-1-yl)-2-buten-1 -ol, 2-ethyl-4-(2,2,3-trimethyl-3- cyclopent-1 -yl)-2
  • aromatic and araliphatic aldehydes and ketones such as, for example, benzaldehyde; phenylacetaldehyde, 3-phenylpropanal, 2-phenyl propanal, 4-methylbenzaldehyde, 4- methylphenylacetaldehyde, 3-(4-ethylphenyl)-2,2-dimethylpropanal, 2-methyl-3-(4- isopropylphenyl)propanal, 2-methyl-3-(4-tert-butylphenyl)propanal, 3-(4-tert- butylphenyl)propanal, cinnamaldehyde, alpha-butylcinnamaldehyde, alpha- amylcinnamaldehyde, alpha-hexylcinnamaldehyde,
  • Naturally occurring exudates such as essential oils extracted from plants may also be used as fragrant components in the invention.
  • Essential oils are usually extracted by processes of steam distillation, solid-phase extraction, cold pressing, solvent extraction, supercritical fluid extraction, hydrodistillation or simultaneous distillation-extraction.
  • Essential oils may be derived from several different parts of the plant, including for example leaves, flowers, roots, buds, twigs, rhizomes, heartwood, bark, resin, seeds and fruits.
  • the major plant families from which essential oils are extracted include Asteraceae, Myrtaceae, Lauraceae, Lamiaceae, Myrtaceae, Rutaceae and Zingiberaceae.
  • the oil is "essential" in the sense that it carries a distinctive scent, or essence, of the plant.
  • Essential oils are understood by those skilled in the art to be complex mixtures which generally consist of several tens or hundreds of constituents. Most of these constituents possess an isoprenoid skeleton with 10 atoms of carbon (monoterpenes), 15 atoms of carbon (sesquiterpenes) or 20 atoms of carbon (diterpenes). Lesser quantities of other constituents can also be found, such as alcohols, aldehydes, esters and phenols.
  • an individual essential oil is usually considered as a single ingredient in the context of practical fragrance formulation. Therefore, an individual essential oil may be considered as a single fragrant component for the purposes of this invention.
  • essential oils for use as fragrant components in the invention include cedarwood oil, juniper oil, cumin oil, cinnamon bark oil, camphor oil, rosewood oil, ginger oil, basil oil, eucalyptus oil, lemongrass oil, peppermint oil, rosemary oil, spearmint oil, tea tree oil, frankincense oil, chamomile oil, clove oil, jasmine oil, lavender oil, rose oil, ylang-ylang oil, bergamot oil, grapefruit oil, lemon oil, lime oil, orange oil, fir needle oil, galbanum oil, geranium oil, grapefruit oil, pine needle oil, caraway oil, labdanum oil, lovage oil, marjoram oil, mandarin oil, clary sage oil, nutmeg oil, myrtle oil, clove oil, neroli oil, patchouli oil, sandalwood oil, thyme oil, verbena oil, vetiver oil and wintergreen oil.
  • the number of different fragrant components contained in the fragrance formulation will generally be at least 4, preferably at least 6, more preferably at least 8 and most preferably at least 10, such as from 10 to 200 and more preferably from 10 to 100.
  • no single fragrant component will comprise more than 70% by weight of the total weight of the fragrance formulation.
  • no single fragrant component will comprise more than 60% by weight of the total weight of the fragrance formulation and more preferably no single fragrant component will comprise more than 50% by weight of the total weight of the fragrance formulation.
  • the term“fragrance formulation” in the context of this invention denotes the fragrant components as defined above, plus any optional excipients. Excipients may be included within fragrance formulations for various purposes, for example as solvents for insoluble or poorly-soluble components, as diluents for the more potent components or to control the vapour pressure and evaporation characteristics of the fragrance formulation.
  • Excipients may have many of the characteristics of fragrant components but they do not have strong odours in themselves. Accordingly, excipients may be distinguished from fragrant components because they can be added to fragrance formulations in high proportions such as 30% or even 50% by weight of the total weight of the fragrance formulation without significantly changing the odour quality of the fragrance formulation.
  • suitable excipients include ethanol, isopropanol, diethylene glycol monoethyl ether, dipropylene glycol, diethyl phthalate and triethyl citrate. Mixtures of any of the above described materials may also be suitable.
  • a suitable fragrance formulation for use in the invention comprises a blend of at least 10 fragrant components selected from hydrocarbons i); aliphatic and araliphatic alcohols ii); aliphatic aldehydes and their acetals iv); aliphatic carboxylic acids and esters thereof viii); acyclic terpene alcohols ix); cyclic terpene aldehydes and ketones xii); cyclic and cycloaliphatic ethers xiii); esters of cyclic alcohols xvi); esters of araliphatic alcohols and aliphatic carboxylic acids xviii); araliphatic ethers and their acetals xix); aromatic and araliphatic aldehydes and ketones xx) and aromatic and araliphatic carboxylic acids and esters thereof xxi); as are further described and exemplified above.
  • the content of fragrant components preferably ranges from 50 to 100%, more preferably from 60 to 100% and most preferably from 75 to 100% by weight based on the total weight of the fragrance formulation; with one or more excipients (as described above) making up the balance of the fragrance formulation as necessary.
  • the fragrance formulation will typically comprise from about 10 to about 60% and preferably from about 20 to about 40% by weight based on the total weight of the benefit agent delivery particle.
  • the amount of fragrance formulation may be measured by taking a slurry of the benefit agent delivery particles, extracting into ethanol and measuring by liquid chromatography.
  • the benefit agent delivery particles of the invention are suitable for incorporation into laundry treatment compositions of all physical forms.
  • the level of benefit agent delivery particles will generally range from 0.01 to 10%, preferably from 0.1 to 5%, more preferably from 0.3 to 3% (by weight based on the total weight of the composition).
  • the benefit agent delivery particles as described above may be separately prepared and then combined with other ingredients to form the final laundry treatment composition.
  • the benefit agent delivery particles may also be formed in situ during preparation of, for example, a liquid laundry detergent including anionic surfactant.
  • cationic surfactant is first deposited onto the exterior surface of the shell of the pre-formed core-shell particles.
  • the mixture of particles is then combined with liquid laundry detergent ingredients including anionic surfactant (as is further described below).
  • Anionic surfactant from the liquid laundry detergent ingredients then forms a complex with the deposited cationic surfactant on the exterior shell surface of the particles.
  • the charged heads of the respective surfactants are neutralized during complexation. If desired, further ingredients may be added to the mixture to form the final liquid laundry detergent.
  • a laundry treatment composition according to the invention is preferably in liquid form.
  • liquid in the context of this invention denotes that a continuous phase or predominant part of the composition is liquid and that the composition is flowable at 15°C and above. Accordingly, the term“liquid” may encompass emulsions, suspensions, and compositions having flowable yet stiffer consistency, known as gels or pastes.
  • the viscosity of the composition may suitably range from about 200 to about 10,000 mPa.s at 25°C at a shear rate of 21 sec 1 . This shear rate is the shear rate that is usually exerted on the liquid when poured from a bottle.
  • Pourable liquid compositions generally have a viscosity of from 200 to 2,500 mPa.s, preferably from 200 to 1500 mPa.s.
  • Liquid compositions which are pourable gels generally have a viscosity of from 1 ,500 mPa.s to 6,000 mPa.s, preferably from 1 ,500 mPa.s to 2,000 mPa.s.
  • the laundry treatment composition according to the invention is a laundry detergent.
  • laundry detergent in the context of this invention denotes formulated compositions intended for and capable of wetting and cleaning domestic laundry such as clothing, linens and other household textiles.
  • the term“linen” is often used to describe certain types of laundry items including bed sheets, pillow cases, towels, tablecloths, table napkins and uniforms.
  • Textiles can include woven fabrics, non-woven fabrics, and knitted fabrics; and can include natural or synthetic fibres such as silk fibres, linen fibres, cotton fibres, polyester fibres, polyamide fibres such as nylon, acrylic fibres, acetate fibres, and blends thereof including cotton and polyester blends.
  • laundry detergents include heavy-duty detergents for use in the wash cycle of automatic washing machines, as well as fine wash and colour care detergents such as those suitable for washing delicate garments (e.g. those made of silk or wool) either by hand or in the wash cycle of automatic washing machines.
  • a laundry detergent according to the invention generally comprises at least 3%, such as from 5 to 60% (by weight based on the total weight of the composition) of one or more detersive surfactants.
  • detersive surfactant and the amount present, will depend on the intended use of the laundry detergent. For example, different surfactant systems may be chosen for hand-washing products and for products intended for use in different types of automatic washing machine.
  • the total amount of surfactant present will also depend on the intended end use and may, in fully formulated products, be as high as 60% (by weight based on the total weight of the composition) in a composition for washing fabrics by hand. In compositions for machine washing of fabrics, an amount of from 5 to 40%, such as 15 to 35% (by weight based on the total weight of the composition) is generally appropriate.
  • detersive surfactant in the context of this invention denotes a surfactant which provides a detersive (i.e. cleaning) effect to laundry treated as part of a domestic laundering process.
  • Preferred detersive surfactants may be selected from non-soap anionic surfactants, nonionic surfactants and mixtures thereof.
  • Non-soap anionic surfactants are principally used to facilitate particulate soil removal.
  • suitable non-soap anionic surfactants for use in the invention include those salts of organic sulfates and sulfonates which are described above in relation to the wash-removable coating, in particular linear alkylbenzene sulfonate (preferably Cn to C1 5 linear alkyl benzene sulfonate) and sodium lauryl ether sulfate (preferably C1 0 to C1 8 alkyl sulfate ethoxylated with an average of 1 to 3 EO) and mixtures thereof.
  • linear alkylbenzene sulfonate preferably Cn to C1 5 linear alkyl benzene sulfonate
  • sodium lauryl ether sulfate preferably C1 0 to C1 8 alkyl sulfate ethoxylated with an average of 1 to 3 EO
  • the total level of non-soap anionic surfactant may suitably range from 5 to 30% (by weight based on the total weight of the composition).
  • Nonionic surfactants may provide enhanced performance for removing very hydrophobic oily soil and for cleaning hydrophobic polyester and polyester/cotton blend fabrics.
  • Nonionic surfactants for use in the invention are typically polyoxyalkylene compounds, i.e the reaction product of alkylene oxides (such as ethylene oxide or propylene oxide or mixtures thereof) with starter molecules having a hydrophobic group and a reactive hydrogen atom which is reactive with the alkylene oxide.
  • Such starter molecules include alcohols, acids, amides or alkyl phenols. Where the starter molecule is an alcohol, the reaction product is known as an alcohol alkoxylate.
  • the polyoxyalkylene compounds can have a variety of block and heteric (random) structures. For example, they can comprise a single block of alkylene oxide, or they can be diblock alkoxylates or triblock alkoxylates.
  • the blocks can be all ethylene oxide or all propylene oxide, or the blocks can contain a heteric mixture of alkylene oxides.
  • examples of such materials include Ce to C22 alkyl phenol ethoxylates with an average of from 5 to 25 moles of ethylene oxide per mole of alkyl phenol; and aliphatic alcohol ethoxylates such as Cs to C18 primary or secondary linear or branched alcohol ethoxylates with an average of from 2 to 40 moles of ethylene oxide per mole of alcohol.
  • a preferred class of nonionic surfactant for use in the invention includes aliphatic Cs to C18, more preferably C12 to C15 primary linear alcohol ethoxylates with an average of from 3 to 20, more preferably from 5 to 10 moles of ethylene oxide per mole of alcohol.
  • the total level of nonionic surfactant may suitably range from 0 to 25% (by weight based on the total weight of the
  • a laundry detergent according to the invention is preferably in liquid form.
  • a liquid laundry detergent according to the invention may generally comprise from 5 to 95%, preferably from 10 to 90%, more preferably from 15 to 85% water (by weight based on the total weight of the composition).
  • the composition may also incorporate non- aqueous carriers such as hydrotropes, co-solvents and phase stabilizers.
  • Such materials are typically low molecular weight, water-soluble or water-miscible organic liquids such as C1 to C5 monohydric alcohols (such as ethanol and n- or i-propanol); C2 to C6 diols (such as monopropylene glycol and dipropylene glycol); C3 to C9 triols (such as glycerol); polyethylene glycols having a weight average molecular weight (M w ) ranging from about 200 to 600; C1 to C3 alkanolamines such as mono-, di- and triethanolamines; and alkyl aryl sulfonates having up to 3 carbon atoms in the lower alkyl group (such as the sodium and potassium xylene, toluene, ethylbenzene and isopropyl benzene (cumene) sulfonates).
  • C1 to C5 monohydric alcohols such as ethanol and n- or i-propanol
  • Non-aqueous carriers when included in a liquid laundry detergent according to the invention, may be present in an amount ranging from 0.1 to 20%, preferably from 1 to 15%, and more preferably from 3 to 12% (by weight based on the total weight of the composition).
  • a laundry detergent according to the invention may contain one or more builders. Builders enhance or maintain the cleaning efficiency of the surfactant, primarily by reducing water hardness. This is done either by sequestration or chelation (holding hardness minerals in solution), by precipitation (forming an insoluble substance), or by ion exchange (trading electrically charged particles).
  • Builders for use in the invention can be of the organic or inorganic type, or a mixture thereof. Non-phosphate builders are preferred.
  • Inorganic, non-phosphate builders for use in the invention include hydroxides, carbonates, silicates, zeolites, and mixtures thereof.
  • Suitable hydroxide builders for use in the invention include sodium and potassium hydroxide.
  • Suitable carbonate builders for use in the invention include mixed or separate, anhydrous or partially hydrated alkali metal carbonates, bicarbonates or sesquicarbonates.
  • the alkali metal is sodium and/or potassium, with sodium carbonate being particularly preferred.
  • Suitable silicate builders include amorphous forms and/or crystalline forms of alkali metal (such as sodium) silicates. Preferred are crystalline layered sodium silicates
  • M is sodium or hydrogen
  • x is a number from 1.9 to 4, preferably 2 or 3
  • y is a number from 0 to 20.
  • Sodium disilicates of the above formula in which M is sodium and x is 2 are particularly preferred. Such materials can be prepared with different crystal structures, referred to as a, b, y and d phases, with d-sodium disilicate being most preferred.
  • Zeolites are naturally occurring or synthetic crystalline aluminosilicates composed of (Si0 4 ) 4 and (AI0 4 ) 5 tetrahedra, which share oxygen-bridging vertices and form cage-like structures in crystalline form.
  • the frameworks acquire their negative charge by substitution of some Si by Al. The negative charge is neutralised by cations and the frameworks are sufficiently open to contain, under normal conditions, mobile water molecules.
  • Suitable zeolite builders for use in the invention may be defined by the general formula (II):
  • x and y are integers of at least 6, the molar ratio of x to y is in the range from about 1 to about 0.5, and z is an integer of at least 5, preferably from about 7.5 to about 276, more preferably from about 10 to about 264.
  • Preferred inorganic, non-phosphate builders for use in the invention may be selected from zeolites (of the general formula (II) defined above), sodium carbonate, d-sodium disilicate and mixtures thereof.
  • Suitable organic, non-phosphate builders for use in the invention include
  • alkali metal e.g. sodium and potassium
  • alkanolammonium salts are preferred.
  • Specific examples of such materials include sodium and potassium citrates, sodium and potassium tartrates, the sodium and potassium salts of tartaric acid monosuccinate, the sodium and potassium salts of tartaric acid disuccinate, sodium and potassium
  • Polymeric polycarboxylates may also be used, such as polymers of unsaturated monocarboxylic acids (e.g. acrylic, methacrylic, vinylacetic, and crotonic acids) and/or unsaturated dicarboxylic acids (e.g. maleic, fumaric, itaconic, mesaconic and citraconic acids and their anhydrides).
  • unsaturated monocarboxylic acids e.g. acrylic, methacrylic, vinylacetic, and crotonic acids
  • unsaturated dicarboxylic acids e.g. maleic, fumaric, itaconic, mesaconic and citraconic acids and their anhydrides
  • Such materials include polyacrylic acid, polymaleic acid, and copolymers of acrylic and maleic acid.
  • the polymers may be in acid, salt or partially neutralised form and may suitably have a molecular weight (Mw) ranging from about 1 ,000 to 100,000, preferably from about 2,000 to about 85,000, and more preferably from about 2,500 to about 75,000.
  • Preferred organic, non-phosphate builders for builders for use in the invention may be selected from polycarboxylates (e.g. citrates) in acid and/or salt form and mixtures thereof.
  • polycarboxylates e.g. citrates
  • the level of phosphate builders in a laundry detergent of the invention is no more than 1 %, more preferably no more than 0.1% and most preferably 0% (by weight based on the total weight of the composition).
  • phosphate builder in the context of this invention denotes alkali metal, ammonium and alkanolammonium salts of polyphosphate, orthophosphate, and/or metaphosphate (e.g. sodium tripolyphosphate).
  • the overall level of builder when included, may range from about 0.1 to about 80%, preferably from about 0.5 to about 50% (by weight based on the total weight of the composition).
  • a laundry detergent according to the invention may also include one or more polymeric cleaning boosters such as antiredeposition polymers, soil release polymers and mixtures thereof.
  • Anti-redeposition polymers stabilise the soil in the wash solution thus preventing redeposition of the soil.
  • Suitable anti-redeposition polymers for use in the invention include alkoxylated polyethyleneimines.
  • Polyethyleneimines are materials composed of ethylene imine units -CH2CH2NH- and, where branched, the hydrogen on the nitrogen is replaced by another chain of ethylene imine units.
  • Preferred alkoxylated polyethyleneimines are materials composed of ethylene imine units -CH2CH2NH- and, where branched, the hydrogen on the nitrogen is replaced by another chain of ethylene imine units.
  • polyethylenimines for use in the invention have a polyethyleneimine backbone of about 300 to about 10000 weight average molecular weight (M w ).
  • the polyethyleneimine backbone may be linear or branched. It may be branched to the extent that it is a dendrimer.
  • the alkoxylation may typically be ethoxylation or propoxylation, or a mixture of both. Where a nitrogen atom is alkoxylated, a preferred average degree of alkoxylation is from 10 to 30, preferably from 15 to 25 alkoxy groups per modification.
  • a preferred material is ethoxylated polyethyleneimine, with an average degree of ethoxylation being from 10 to 30, preferably from 15 to 25 ethoxy groups per ethoxylated nitrogen atom in the polyethyleneimine backbone.
  • Another type of suitable anti-redeposition polymer for use in the invention includes cellulose esters and ethers, for example sodium
  • the overall level of anti-redeposition polymer when included, may range from 0.05 to 6%, more preferably from 0.1 to 5% (by weight based on the total weight of the composition).
  • Soil release polymers help to improve the detachment of soils from fabric by modifying the fabric surface during washing.
  • the adsorption of a SRP over the fabric surface is promoted by an affinity between the chemical structure of the SRP and the target fibre.
  • SRPs for use in the invention may include a variety of charged (e.g. anionic) as well as non-charged monomer units and structures may be linear, branched or star-shaped.
  • the SRP structure may also include capping groups to control molecular weight or to alter polymer properties such as surface activity.
  • the weight average molecular weight (M w ) of the SRP may suitably range from about 1000 to about 20,000 and preferably ranges from about 1500 to about 10,000.
  • SRPs for use in the invention may suitably be selected from copolyesters of dicarboxylic acids (for example adipic acid, phthalic acid or terephthalic acid), diols (for example ethylene glycol or propylene glycol) and polydiols (for example polyethylene glycol or polypropylene glycol).
  • the copolyester may also include monomeric units substituted with anionic groups, such as for example sulfonated isophthaloyl units.
  • oligomeric esters produced by transesterification/oligomerization of poly(ethyleneglycol) methyl ether, dimethyl terephthalate (“DMT”), propylene glycol (“PG”) and poly(ethyleneglycol) (“PEG”); partly- and fully-anionic-end-capped oligomeric esters such as oligomers from ethylene glycol (“EG”), PG, DMT and Na-3,6-dioxa-8- hydroxyoctanesulfonate; nonionic-capped block polyester oligomeric compounds such as those produced from DMT, Me-capped PEG and EG and/or PG, or a combination of DMT, EG and/or PG, Me-capped PEG and Na-dimethyl-5-sulfoisophthalate, and copolymeric blocks of ethylene terephthalate or propylene terephthalate with polyethylene oxide or polypropylene oxide terephthalate
  • cellulosic derivatives such as hydroxyether cellulosic polymers, Ci-C4 alkylcelluloses and C 4 hydroxyalkyl celluloses
  • Preferred SRPs for use in the invention include copolyesters formed by condensation of terephthalic acid ester and diol, preferably 1 ,2 propanediol, and further comprising an end cap formed from repeat units of alkylene oxide capped with an alkyl group. Examples of such materials have a structure corresponding to general formula (I):
  • R 1 and R 2 independently of one another are X-(OC2H4) n -(OC3H6) m ;
  • X is C1-4 alkyl and preferably methyl
  • n is a number from 12 to 120, preferably from 40 to 50;
  • n is a number from 1 to 10, preferably from 1 to 7;
  • a is a number from 4 to 9. Because they are averages, m, n and a are not necessarily whole numbers for the polymer in bulk.
  • the overall level of SRP when included, may range from 0.1 to 10%, preferably from 0.3 to 7%, more preferably from 0.5 to 5% (by weight based on the total weight of the composition).
  • Transition metal ion chelating agents
  • a liquid or particulate laundry detergent according to the invention may contain one or more chelating agents for transition metal ions such as iron, copper and manganese. Such chelating agents may help to improve the stability of the composition and protect for example against transition metal catalysed decomposition of certain ingredients.
  • Suitable transition metal ion chelating agents include phosphonates, in acid and/or salt form. When utilized in salt form, alkali metal (e.g. sodium and potassium) or
  • alkanolammonium salts are preferred.
  • specific examples of such materials include aminotris(methylene phosphonic acid) (ATMP), 1-hydroxyethylidene diphosphonic acid (HEDP) and diethylenetriamine penta(methylene phosphonic acid (DTPMP) and their respective sodium or potassium salts.
  • HEDP is preferred.
  • Mixtures of any of the above described materials may also be used.
  • Transition metal ion chelating agents when included, may be present in an amount ranging from about 0.1 to about 10%, preferably from about 0.1 to about 3% (by weight based on the total weight of the composition).
  • a laundry detergent according to the invention may in some cases contain one or more fatty acids and/or salts thereof.
  • Suitable fatty acids in the context of this invention include aliphatic carboxylic acids of formula RCOOH, where R is a linear or branched alkyl or alkenyl chain containing from 6 to 24, more preferably 10 to 22, most preferably from 12 to 18 carbon atoms and 0 or 1 double bond.
  • Preferred examples of such materials include saturated C12-18 fatty acids such as lauric acid, myristic acid, palmitic acid or stearic acid; and fatty acid mixtures in which 50 to 100% (by weight based on the total weight of the mixture) consists of saturated C12-18 fatty acids.
  • Such mixtures may typically be derived from natural fats and/or optionally hydrogenated natural oils (such as coconut oil, palm kernel oil or tallow).
  • the fatty acids may be present in the form of their sodium, potassium or ammonium salts and/or in the form of soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • Fatty acids and/or their salts when included, may be present in an amount ranging from about 0.25 to 5%, more preferably from 0.5 to 5%, most preferably from 0.75 to 4% (by weight based on the total weight of the composition).
  • fatty acids and/or their salts are not included in the level of surfactant or in the level of builder.
  • a liquid laundry detergent according to the invention may comprise one or more rheology modifiers.
  • rheology modifiers include polymeric thickeners and/or structurants such as hydrophobically modified alkali swellable emulsion (HASE) copolymers.
  • Exemplary HASE copolymers for use in the invention include linear or crosslinked copolymers that are prepared by the addition polymerization of a monomer mixture including at least one acidic vinyl monomer, such as (meth)acrylic acid (i.e. methacrylic acid and/or acrylic acid); and at least one associative monomer.
  • the term“associative monomer” in the context of this invention denotes a monomer having an ethylenically unsaturated section (for addition polymerization with the other monomers in the mixture) and a hydrophobic section.
  • a preferred type of associative monomer includes a polyoxyaikylene section between the ethylenically unsaturated section and the
  • Preferred HASE copolymers for use in the invention include linear or crosslinked copolymers that are prepared by the addition polymerization of (meth)acrylic acid with (i) at least one associative monomer selected from linear or branched C8-C40 alkyl (preferably linear C12-C22 alkyl) polyethoxylated (meth)acrylates; and (ii) at least one further monomer selected from C1-C4 alkyl (meth) acrylates, polyacidic vinyl monomers (such as maleic acid, maleic anhydride and/or salts thereof) and mixtures thereof.
  • the polyethoxylated portion of the associative monomer (i) generally comprises about 5 to about 100, preferably about 10 to about 80, and more preferably about 15 to about 60 oxyethylene repeating units.
  • Polymeric thickeners when included, may be present in an amount ranging from 0.1 to 5% (by weight based on the total weight of the composition).
  • a liquid laundry detergent according to the invention may also have its rheology modified by use of one or more external structurants which form a structuring network within the composition.
  • external structurants include hydrogenated castor oil, microfibrous cellulose and citrus pulp fibre.
  • the presence of an external structurant may provide shear thinning rheology and may also enable materials such as encapsulates and visual cues to be suspended stably in the liquid.
  • a laundry detergent according to the invention may comprise an effective amount of one or more enzymes selected from the group comprising, pectate lyase, protease, amylase, cellulase, lipase, mannanase and mixtures thereof.
  • the enzymes are preferably present with corresponding enzyme stabilizers.
  • a liquid laundry detergent according to the invention preferably has a pH in the range of 5 to 9, more preferably 6 to 8, when measured on dilution of the composition to 1% (by weight based on the total weight of the composition) using demineralised water.
  • a laundry treatment composition of the invention may contain further optional ingredients to enhance performance and/or consumer acceptability.
  • ingredients include foam boosting agents, preservatives (e.g. bactericides), antioxidants, sunscreens, anticorrosion agents, colorants, pearlisers and/or opacifiers, and shading dye.
  • foam boosting agents e.g. bactericides
  • preservatives e.g. bactericides
  • sunscreens e.g. bactericides
  • anticorrosion agents e.g. bactericides
  • colorants e.g. bactericides
  • pearlisers and/or opacifiers e.g. opacifiers
  • these optional ingredients are included individually at an amount of up to 5% (by weight based on the total weight of the composition).
  • a laundry treatment composition of the invention may be packaged as unit doses in polymeric film soluble in the wash water.
  • a composition of the invention may be supplied in multidose plastics packs with a top or bottom closure.
  • a dosing measure may be supplied with the pack either as a part of the cap or as an integrated system.
  • a method of treating fabric using a laundry detergent according to the invention will usually involve diluting the dose of detergent to obtain a wash liquor, and washing fabrics with the wash liquor so formed.
  • the method of laundering fabric may suitably be carried out in an automatic washing machine, or can be carried out by hand.
  • the dose of detergent is typically put into a dispenser and from there it is flushed into the machine by the water flowing into the machine, thereby forming the wash liquor.
  • the dose of detergent may be added directly into the drum.
  • Dosages for a typical front-loading washing machine (using 10 to 15 litres of water to form the wash liquor) may range from about 10 ml to about 60 ml, preferably about 15 to 40 ml.
  • Dosages for a typical top-loading washing machine (using from 40 to 60 litres of water to form the wash liquor) may be higher, e.g. up to about 100 ml. Lower dosages of detergent (e.g.
  • any input of water during any optional rinsing step(s) is not included when determining the volume of the wash liquor.
  • the laundry drying step can take place either in an automatic dryer or in the open air.
  • Melamine-formaldehyde core-shell particles were prepared having a shell of melamine- formaldehyde, a core containing a 15-component model fragrance, an average particle diameter of approximately 13pm and a zeta potential of approximately -20mV (when measured as described above). The particles were obtained in an aqueous slurry having a solids content of about 30 wt.%. A laundry liquid was separately prepared having ingredients shown in Table 1.
  • the aqueous particle slurry was diluted with water to reduce the solids content to about 10 wt.%.
  • a formulation according to the invention (Example 1 ) was prepared by first adding CTAC (cetyl trimethylammonium chloride) to the 10 wt% aqueous particle slurry and mixing for 30 minutes. A 1 ml aliquot of the CTAC-treated particle slurry so obtained was then mixed with 9ml of the laundry liquid to form the Example 1 formulation.
  • a control formulation was also prepared by adding a 1 ml aliquot of the 10 wt.% aqueous particle slurry (not mixed with CTAC) to 9ml of the laundry liquid.
  • test samples of the control and Example 1 formulations respectively were placed on a roller for 24 hours, followed by centrifugation for 30 minutes at 1 10OOrpm. The supernatant liquid was then removed and filtered through a 3.1 pm filter. 1 ml of the filtrate was then placed in a 20ml headspace vial. The headspace above the filtrate was measured after incubation for 10 minutes at 40°C on a CombiPAL autosampler. Sampling was achieved using a DMS/Carboxen/DVB fibre with an exposure time of 60 seconds. The fibre was then desorbed for 5 minutes at 270°C in the inlet of an Agilent 6890 gas chromatograph.
  • Example 1 demonstrate a significantly lower fragrance leakage percentage than the uncoated control particles when incorporated into laundry liquid.
  • the laundry liquid is diluted in a washing operation (typically 35ml liquid into 21 L water) the coating is removed.
  • the particles of the invention provide an improvement in the stability of the fragrance toward leakage in product, whilst providing an enhanced fragrance experience in the early stages post wash.

Abstract

L'invention concerne une particule de distribution d'agent bénéfique présentant une structure cœur-écorce dans laquelle une écorce poreuse de matériau polymère piège un cœur contenant l'agent bénéfique ; dans laquelle les pores dans l'écorce sont au moins partiellement occlus par un revêtement éliminable par lavage disposé au niveau de la surface extérieure de l'écorce ; et caractérisée en ce que le revêtement éliminable par lavage est formé à partir de particules déposées d'un complexe d'un tensioactif cationique et d'un tensioactif anionique. L'invention concerne également une composition de traitement du linge comprenant une particule de distribution d'agent bénéfique telle que définie ci-dessus.
PCT/EP2019/069044 2018-07-17 2019-07-15 Particules de distribution d'agent bénéfique WO2020016194A1 (fr)

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CN201980047653.6A CN112567013B (zh) 2018-07-17 2019-07-15 有益剂递送颗粒
EP19737568.6A EP3824061B1 (fr) 2018-07-17 2019-07-15 Particules de distribution d'agent bénéfique
BR112021000737-7A BR112021000737B1 (pt) 2018-07-17 2019-07-15 Partículas de distribuição de agente de benefício, processo de preparação de partícula de distribuição de agente de benefício e composição de tratamento para a lavagem de roupas
ZA2021/00030A ZA202100030B (en) 2018-07-17 2021-01-04 Benefit agent delivery particles

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022152689A1 (fr) * 2021-01-13 2022-07-21 Unilever Ip Holdings B.V. Particules d'administration d'agent bénéfique

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060172909A1 (en) * 2003-06-13 2006-08-03 Peter Schmiedel Peroxycarboxylic acid-based polyelectrolyte capsule system having a long shelf life
WO2009103576A1 (fr) * 2008-02-21 2009-08-27 Unilever Plc Agent bénéfique encapsulé
US20160376535A1 (en) * 2009-11-06 2016-12-29 The Procter & Gamble Company Hepmc
US20180009996A1 (en) * 2016-07-11 2018-01-11 Microtek Laboratories Inc. Capsules having surfactant tethered outer shells and methods for making same

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10241942A1 (de) * 2002-09-10 2004-03-18 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Mikrokapseln für die Kautschukherstellung und Verfahren zu deren Herstellung
US20070138671A1 (en) * 2005-12-15 2007-06-21 Anastasiou Theodore J Encapsulated active material with reduced formaldehyde potential
ES2713983T3 (es) * 2012-10-24 2019-05-24 Unilever Nv Mejoras relacionadas con agentes beneficiosos encapsulados
CN105121616A (zh) * 2013-04-24 2015-12-02 宝洁公司 香料体系
CN105492588A (zh) * 2013-08-28 2016-04-13 宝洁公司 包含微胶囊的洗涤剂或清洁剂
US9610228B2 (en) * 2013-10-11 2017-04-04 International Flavors & Fragrances Inc. Terpolymer-coated polymer encapsulated active material
WO2016023145A1 (fr) * 2014-08-11 2016-02-18 The Procter & Gamble Company Détergent textile
CN106999896B (zh) * 2014-12-16 2020-10-30 诺赛尔股份有限公司 包衣微胶囊
WO2016176241A1 (fr) * 2015-04-29 2016-11-03 The Procter & Gamble Company Composition détergente
CA2985473A1 (fr) * 2015-05-29 2016-12-08 The Procter & Gamble Company Compositions assouplissantes fluides pour textile

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060172909A1 (en) * 2003-06-13 2006-08-03 Peter Schmiedel Peroxycarboxylic acid-based polyelectrolyte capsule system having a long shelf life
WO2009103576A1 (fr) * 2008-02-21 2009-08-27 Unilever Plc Agent bénéfique encapsulé
US20160376535A1 (en) * 2009-11-06 2016-12-29 The Procter & Gamble Company Hepmc
US20180009996A1 (en) * 2016-07-11 2018-01-11 Microtek Laboratories Inc. Capsules having surfactant tethered outer shells and methods for making same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022152689A1 (fr) * 2021-01-13 2022-07-21 Unilever Ip Holdings B.V. Particules d'administration d'agent bénéfique

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CN112567013A (zh) 2021-03-26
BR112021000737B1 (pt) 2024-01-09
ZA202100030B (en) 2022-07-27
EP3824061A1 (fr) 2021-05-26
EP3824061B1 (fr) 2023-03-29
CN112567013B (zh) 2023-05-26

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