BENEFIT AGENT DELIVERY PARTICLES

The present invention relates to delivery particles for benefit agents for use in the treatment of fabrics and compositions (such as laundry treatment compositions) comprising such particles.

Benefit agents offer fabric treatment e.g. care benefits but are expensive and can have poor efficacy when employed even at high levels in aqueous treatment processes, especially those involving surfactants particularly linear alkylbenzene sulfonates.

Effective encapsulation techniques typically comprise polymers such as melamine formaldehyde polymers. However, consumer find these are less desirable environmentally.

Despite the prior art, there remains a need for environmentally friendly delivery particles which can be used to deliver fabric benefits such as care benefits in laundry formulations, especially LAS-containing formulations.

The invention provides in a first aspect a benefit agent delivery particle comprising a coreshell structure in which a shell of polymeric material entraps a core containing a nonvolatile benefit agent, wherein said shell comprises a polyester.

In a second aspect the invention provides a laundry treatment composition comprising a non-volatile benefit agent delivery particle as defined above.

In a further aspect the invention provides a method of making a benefit agent delivery particle according to first aspect of the invention, the method comprising the step of encapsulating a non-volatile benefit agent with a polyester.

In a yet further aspect, the invention provides a method of making a laundry treatment composition comprising adding a non-volatile benefit agent delivery particle to said composition. The arrangement of the invention allows for efficient and effective encapsulation of nonvolatile benefit agents and for their efficient deposition to fabrics which are thereby more effectively treated (by the benefit agent). The particles perform when formulated in laundry treatment compositions, including LAS-rich compositions providing a measurable improvement to said fabric by means of the deposited benefit agent.

Definitions

As used herein, the following terms are defined:

The articles “a” and “an” when used in a claim, are understood to mean one or more of what is claimed or described; and "include", "includes" and "including" are meant to be non-limiting.

“Alkyl” means an unsubstituted or substituted saturated hydrocarbon chain having from 1 to 18 carbon atoms. The chain may be linear or branched.

"Biodegradable" means the ability of a compound to ultimately be degraded completely into CO2 and water or biomass by microorganisms and/or natural environmental factors, preferably within 6 months.

“Detergent composition” in the context of this invention denotes formulated detergent (cleaning) compositions, generally containing detersive surfactants, and intended for and capable of treating substrates as defined herein

“Detersive surfactant” in the context of this invention denotes a surfactant which provides a detersive (i.e. cleaning) effect to a substrate such as fabric treated as part of a domestic treatment e.g. laundering process.

“Encapsulate” encompasses microcapsules, including “benefit agent containing microcapsules@ and the terms “core-shell particles”, “encapsulate” or “benefit agent containing delivery particle” and “microcapsule” are synonymous and may be used interchangeably and may further comprise deposition aids as herein described.

Linking agent” is used interchangeably with “coupling agent” and “grafting agent”, “Washing operation” as used herein generally denotes a method of laundering fabric using a laundry treatment composition according to the invention.

"Substantially free of' or "substantially free from" refers to either the complete absence of an ingredient or a minimal amount thereof merely as impurity or unintended by-product of another ingredient. A composition that is "substantially free" of/from a component means that the composition comprises less than 0.5%, 0.25%, 0.1%, 0.05%, or 0.01 %, or even 0%, by weight of the composition, of the component.

"Size" refers to diameter unless otherwise stated. For samples with particle diameter no greater than 1 micron, 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 Nano™ ZS90 (Malvern Instruments Ltd, UK). For samples with particle diameter greater than 1 micron, 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 Mastersizer™ 2000 (Malvern Instruments Ltd, UK).

"Substrate” preferably is any suitable substrate and includes but is not limited to fabric substrates. Fabric substrates includes clothing, linens and other household textiles etc. In the context of fabrics, wherein the term “linen” is used to describe certain types of laundry items including bed sheets, pillow cases, towels, tablecloths, table napkins and uniforms and the term “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.

“Treatment” in the context of treating substrates may include cleaning, soil removal, stain removal conditioning, lubricating, care, softening, easy-ironing, anti-wrinkle, fragrancing, de-pilling, rejuvenation preferably including colour rejuvenation (reduction in colour fade), colour treatments soaking, washing, pre-treatment of substrates, bleaching, and any combination thereof. llnless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.

Dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a value disclosed as "50 microns’ is intended to mean "about 50 microns."

All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. It should be understood that every maximum numerical limitation given throughout this specification includes every lower numerical limitation, as if such lower numerical limitations were expressly written herein. Every minimum numerical limitation given throughout this specification will include every higher numerical limitation, as if such higher numerical limitations were expressly written herein. Every numerical range given throughout this specification will include every narrower numerical range that falls within such broader numerical range, as if such narrower numerical ranges were all expressly written herein

Benefit agent delivery particle

The core of the particle is suitably formed in an inner region, inner being relative to the shell. Particles may be prepared using methods known to those skilled in the art such as coacervation, interfacial polymerization, and polycondensation.

The process of coacervation typically involves encapsulation of a generally waterinsoluble 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 subsequent core-shell particles. Shell-forming materials (monomers or oligomers) 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 and form core-shell particles. An example of a core-shell particle produced by this method is a polyurea core-shell particle with a shell formed by reaction of diisocyanates or polyisocyanates with diamines or polyamines.

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 core-shell particles. An example of a core-shell particle produced by this method is an aminoplast core-shell particle with a shell formed from the polycondensation product of 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) may also be used and secondary wall polymers may also be used as appropriate, e.g. anhydrides and their derivatives, particularly polymers and co-polymers of maleic anhydride.

Polyester shell

The polyester may comprise a synthetic or natural polyester.

Preferably the polyester is hydrophobic.

Preferably the shell comprises an aliphatic polyester. More preferably the shell comprises a biodegradable polyester, and in this regard most preferably the shell comprises a linear aliphatic polyester. Firmicutes and proteobacteria can degrade PCL.[9] Penicillium sp. strain 26-1 can degrade high density PCL; though not as quickly as thermotolerant Aspergillus sp. strain ST-01. Species of Clostridium can degrade PCL under anaerobic conditions

The polyester may comprise a synthetic or natural polyester.

Polyesters may be produced by biosynthesis using fermentation, using random polymerization, ring opening polymerization, and the block copolymerization techniques. The polyester may comprise any of polylactic acid (PLA), polyglycolic acid (PGA), poly-e- caprolactone (PCL), polyhydroxybutyrate (PHB), and poly(3-hydroxy valerate), poly(ethylene succinate) (PESu), polypropylene succinate) (PPSu) and poly(butylene succinate) (PBSu), polyhydroxyhexanoate, polyhydroxyoctanoate or any combination or thereof.

Homo polymers are preferred.

Preferably the polyester may comprise any of poly-e-caprolactone (PCL), polyhydroxybutyrate (PHB), and poly(3-hydroxy valerate), poly(ethylene succinate) (PESu), polypropylene succinate) (PPSu) and polyputylene succinate) (PBSu), polyhydroxyhexanoate, polyhydroxyoctanoate or any combination or thereof.

Polylactic acid PLA, or polylactide is a thermoplastic polyester with backbone formula _n or [-CHCO-] _n , formally obtained by condensation of lactic acid CHCOOH with loss of water. It can also be prepared by ring-opening polymerization of lactide [-CHCO-] ₂ , the cyclic dimer of the basic repeating unit.

PHB entirely is biosynthesized by an efficient fermentation process with different molecular weight (from 200 to 1500 kDa) using diazotrophic bacteria of acetobacter and Rhizobium genus.

Co-polymers comprising any of the above polyesters or blends of co-polymers are included in the invention. 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 core-shell particle.

The particles preferably have an average particle size between 100 nanometers and 50 microns. Particles larger than this are entering the visible range.

The particles may have an average particle size of from 0.6 to 50 microns.

One benefit of small particles is that they can deposit via diffusion onto fibres of fabric. Accordingly the core shell particles may have an average particle size of from 0.6 - 1 micron.

However, larger particles are preferred. Larger particles deposit by filtration: they impact the fibres and become lodged thereon. Thus, advantageously the particles have an average particle size of at least 9 microns, even more preferably at least 10 microns, and most preferably at least 15 microns. The larger particles preferably have an average particle size of not more than 50 microns, more preferably not more than 40 microns, even more preferably not more than 30 microns, most preferably not more than 20 microns.

In some embodiments, the average particle size is preferably 10- 30 microns, more preferably 15 - 20 microns.

The particle size distribution can be narrow, broad or multimodal. If necessary, the coreshell particles as initially produced may be filtered or screened to produce a product of greater size uniformity.

Charge

Core-shell particles suitable for use in the invention may be positively or negatively charged. However, it is preferred that the core-shell particles are negatively charged 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 Nano™ ZS90 (Malvern Instruments Ltd, UK) at 25° C. A dispersion of the core-shell particles in deionised water with a solids content of around 500 ppm and a pH adjusted to about 7 is used for the measurement.

Deposition Aids

The particles of the invention are preferably provided with a deposition aid at the outer surface of the particle. Deposition aids can modify the properties of the exterior of the particle to make the particle more substantive to a specific substrate. Advantageously, the deposition aid is substantive to fabric substrates as defined herein, but preferably including cellulosics (including cotton) and/or polyesters (including those employed in the manufacture of polyester fabrics).

The deposition aid may suitably be provided at the outer surface of the particle by means of covalent bonding, entanglement or strong adsorption. The deposition aid is preferably attached to the outside of the shell, and preferably by means of covalent bonding.

The deposition may be attached directly to shell.

The deposition aid may be present at 0.1-10wt %, preferably 1-5 wt%, more preferably 1.5 to 3wt%, most preferably 2wt% based on total weight of the encapsulate.

The deposition aid may be attached to the encapsulate as part of the encapsulation process, so peri-encapsulation (generally in the latter stages of a time period in which encapsulation takes place) or post encapsulation (after completion of the encapsulation process). In the latter case, this may involve use of a pre-polymer (e.g. trimethylolmelamine for aminoplast shells e.g. melamine formaldehyde shells) which can be added with the deposition aid.

While it is preferred that the deposition aid is attached directly to the outside of the shell, it may also be attached via a linking species. The deposition aid is preferably covalently bonded to the outer surface of the microcapsule shell.

The deposition aid may comprise a nonionic polysaccharide polymer. The nonionic polysaccharide polymer may comprise branched and unbranched materials having a - 1 ,4- backbone and of branched and unbranched materials having a p-1 ,3-linked backbone. Preferably the nonionic polysaccharide polymer comprises branched and unbranched materials having a p-1 ,4- backbone.

Deposition aids for use in the invention may suitably be selected from polysaccharides having an affinity for cellulose. Such 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 glycan (generalised sugar) backbone structure with at least 4, and preferably at least 10 backbone residues which are pi -4 linked, such as a glucan backbone (consisting of 1 -4 linked glucose residues), a mannan backbone (consisting of pi -4 linked mannose residues) or a xylan backbone (consisting of pi -4 linked xylose residues). Preferred pi -4 linked polysaccharides include xyloglucans, glucomannans, mannans, galactomannans, P(1 -3), (1 -4) glucan and the xylan family incorporating glucurono-, arabino- and glucuronoarabinoxylans.

More preferably the deposition aids comprises xyloglucans or galactomannans.

Preferred depositions aids may be selected from xyloglucans of plant origin, such as pea xyloglucan and tamarind seed xyloglucan (TXG) (which has a pi -4 linked glucan backbone with side chains of a-D xylopyranose and p-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 pi -4 linked mannose residues, with single unit galactose side chains linked a1 -6 to the backbone).

Most preferred are xyloglucans.

Also suitable are 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 (HPC) , 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. Such 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. Typically, 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.

Mixtures of any of the above described materials may also be suitable.

In one embodiment, the microcapsules shell maybe coated with polymer to enhance the ability of the microcapsule to adhere to fabric, as describe in U.S. Patent Nos. 7,125,835; 7,196,049; and 7,119,057.

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 about 10 kDa to about 500 kDa and more preferably from about 20 kDa to about 300 kDa.

Method of Manufacture

The method of making a benefit agent delivery particle according to the invention may include the pre-step of emulsifying the benefit agent with an emulsifier. This step is preferably carried out prior to adding the benefit agent to shell material.

Emulsifiers include any colloidal stabilisers or surfactants. Preferably the emulsifier a low-foaming emulsifier. Preferably the emulsifier is a polymeric colloidal stabliser. A preferred polymer is PVOH. Other examples include sorbitan esters, polysorbates and blends of these. Synthetic water soluble polymers which are suitable include:

(1) polyvinyl pyrrolidone;

(2) water soluble celluloses;

(3) polyvinyl alcohol;

(4) ethylene maleic anhydride copolymer;

(5) methyl vinyl ether maleic anhydride copolymer; (6) polyethylene oxides;

(7) water soluble polyamide or polyester;

(8) copolymers or homopolymers of acrylic acid such as polyacrylic acid, polystyrene acrylic acid copolymers or mixtures of two or more.

The method preferably includes the step of attaching to said shell a deposition aid such as any of the deposition aids described herein. The step of attaching the deposition aid to said shell using a linking agent. The linking agent may be homobifunctional (same reactive groups) or heterobifunctional (different reactive groups). The linking agent may be a water soluble carbodiimide. A preferred water soluble carbodiimide is ethyl-3-(3- dimethylaminopropyl) carbodiimide (EDC, EDAC).

Benefit Agents

Preferred benefit agents in the context of fabric treatment exclude fragrance formulations and are restricted to non-volatile benefit agents. Non-volatile agents provide technical benefits which differ those coming from volatile actives such as fragrances. Non-volatile agents do not rely on olfactory perception but instead provide tactile or visual effects e.g. softness or colour benefits such as a reduction in colour fade.

Examples include any of clays, enzymes, antifoams, fluorescers, bleaching agents and precursors thereof (including photo-bleach), dyes and/or pigments, 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, ceramides, reducing agents, sequestrants, 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) and antimicrobial or microbe control agents. Mixtures of any of the above-described materials may also be suitable.

In this specification a “non-volatile benefit agent” means a benefit agent that does not volatilise too much. A perfume is not non-volatile. When applied to a surface and left at 25 °C a non-volatile material will lose less than 50% of its mass over a time of 7 days. A non-volatile functional material typically has a boiling point greater than 250 °C. Examples of non-volatile benefit agents include silicone oils or natural e.g. ester oils. Such oils can provide care benefits arising from non-volatile actives (so not olfactory but tactile or visual effects) e.g. softness or colour benefits such as a reduction in colour fade.

Oil

The oil may be a natural oil or a synthetic oil such as a silicone or a modified natural oil or any combination thereof, provided it is non-volatile.

Natural oils

Natural oils preferably comprise plant oils, and exclude mineral oils derived from petroleum.

Plant oils

Suitable plant oils include vegetable, nut and seed oils. Plant oils include microbial oils, which are oils that produced by microbes or other organisms, including algal oils and including genetically modified or engineered microbes that produce oils.

Seed oils

Suitable seed oils include almond, argan, babassu, borage, camelina , canola ®, castor, chia, cherry, coconut, corn, cotton, coffee, Cuphea Viscosissima , flax (linseed), grape, hemp, hepar, jatropha, jojoba, Lesquerella Fendleri oil, Moringa Oleifera oil, macadamia, mango, mustard, neem, oil palm, perilla, rapeseed, safflower, sesame, shea, stillingia, soybean, sunflower, tonka bean, tung.

Vegetable Oils

Suitable vegetable oils include olive oil, palm, rice bran oils.

Ester Oil

If utilised, preferably, the ester oil is hydrophobic. The ester oil may be a sugar ester oil or an oil with substantially no surface activity. Preferably the oil is a liquid or soft solid. Preferably, the oil is polyol ester (i.e. more than one alcohol group is reacted to form the polyol ester). Preferably the polyol ester is formed by esterification of a polyol (i.e. reacting a molecule comprising more than one alcohol group with acids). Preferably the polyol ester comprises at least two ester linkages. Preferably the polyol ester comprises no hydroxyl groups.

Preferably the ester oil is a pentaerythritol e.g. a pentaerythritol tetraisostearate.

Exemplary structures of the compound are (I) and (II) below:

Preferably the oil is saturated.

Preferably, the ester oils are esters containing straight or branched, saturated or unsaturated carboxylic acids.

Suitable ester oils are the fatty ester of a mono or polyhydric alcohol having from 1 to about 24 carbon atoms in the hydrocarbon chain and mono or polycarboxylic acids having from 1 to about 24 carbon atoms in the hydrocarbon chain with the proviso that the total number of carbon atoms in the ester oil is equal to or greater than 16 and that at least one of the hydrocarbon radicals in the ester oil has 12 or more carbon atoms.

Preferably the viscosity of the ester oil or mineral oil is from 2 mPa. s to 400 mPa. s at a temperature of 25 C, more preferably a viscosity from 2 to 150 mPa. s, most preferably a viscosity from 10 to 100 mPa. s.

Preferably the refractive index of the oil is from 1.445 to 1.490, more preferred from 1.460 to 1.485. Silicone

The oil may comprise silicone. The silicone is preferably present in the formed of dispersed droplets. Thus, the term ‘particle’ as used in relation to silicone, as used herein, mean ‘droplet’.

Silicone (oil) may be present at a level selected from: less than 10 %, less than 5 %, and less than 2.5 %, by weight of the laundry detergent composition. Silicone may be present at a level selected from: more than 0.01 %, more than 0.05 %, and more than 0.1 %, by weight of the composition. Suitably silicone is present in the composition in an amount selected from the range of from about 0.01 % to about 10 %, preferably from about 0.05 % to about 5 %, more preferably from about 0.1 % to about 2.5 %, by weight based on the total weight of the composition.)

Silicones suitable for the present invention are fabric softening silicones. Non-limiting examples of such silicones include:

• Non-functionalised silicones such as polydimethylsiloxane (PDMS),

• Functionalised silicones such as alkyl (or alkoxy) functionalised, alkylene oxide functionalised, amino functionalised, phenyl functionalised, hydroxy functionalised, polyether functionalised, acrylate functionalised, siliconhydride functionalised, carboxy functionalised, phosphate functionalised, sulphate functionalised, phosphonate functionalised, sulphonic functionalised, betaine functionalised, quarternized nitrogen functionalised and mixtures thereof.

• Copolymers, graft co-polymers and block co-polymers with one or more different types of functional groups such as alkyl, alkylene oxide, amino, phenyl, hydroxy, polyether, acrylate, siliconhydride, carboxy, phosphate, sulphonic, phosphonate, betaine, quarternized nitrogen and mixtures thereof.

Suitable non-functionalised silicones have the general formula:

R1 - Si(R3)2 - O - [- Si(R3)2 - O -]x - Si(R3)2 - R2

R1 = hydrogen, methyl, methoxy, ethoxy, hydroxy, propoxy, and aryloxy group. R2 = hydrogen, methyl, methoxy, ethoxy, hydroxy, propoxy, and aryloxy group. R3 = alkyl, aryl, hydroxy, or hydroxyalkyl group, and mixtures thereof Suitable functionalised silicones may be anionic, cationic, or non-ionic functionalised silicones.

The functional group(s) on the functionalised silicones are preferably located in pendent positions on the silicone i.e. the composition comprises functionalised silicones wherein the functional group(s) are located in a position other than at the end of the silicone chain. The terms ‘terminal position’ and ‘at the end of the silicone chain’ are used to indicate the terminus of the silicone chain.

When the silicones are linear in nature, there are two ends to the silicone chain. In this case the anionic silicone preferably contains no functional groups located on a terminal position of the silicone.

When the silicones are branched in nature, the terminal position is deemed to be the two ends of the longest linear silicone chain. Preferably no functional group(s) are located on the terminus of the longest linear silicone chain.

Preferred functionalised silicones are those that comprise the anionic group at a midchain position on the silicone. Preferably the functional group(s) of the functionalised silicone are located at least five Si atoms from a terminal position on the silicone. Preferably the functional groups are distributed randomly along the silicone chain.

For best performance, it is preferred that the silicone is selected from: anionic functionalised silicone, non-functionalised silicone; and mixtures thereof. More preferably, the silicone is selected from: carboxy functionalised silicone; amino functionalised silicone; polydimethylsiloxane (PDMS) and mixtures thereof. Preferred features of each of these materials are outlined herein.

A carboxy functionalised silicone may be present as a carboxylic acid or an carbonate anion and preferably has a carboxy group content of at least 1 mol% by weight of the silicone polymer, preferably at least 2 mol%. Preferably the carboxy group(s) are located in a pendent position, more preferably located at least five Si atoms from a terminal position on the silicone. Preferably the caboxy groups are distributed randomly along the silicone chain. Examples of suitable carboxy functional silicones include FC 220 ex. Wacker Chemie and X22-3701E ex. Shin Etsu.

An amino functionalised silicone means a silicone containing at least one primary, secondary or tertiary amine group, or a quaternary ammonium group. The primary, secondary, tertiary and/or quaternary amine groups are preferably located in a pendent position, more preferably located at least five Si atoms from a terminal position on the silicone. Preferably the amino groups are distributed randomly along the silicone chain. Examples of suitable amino functional silicones include FC222 ex. Wacker Chemie and EC218 ex. Wacker Chemie.

A polydimethylsiloxane (PDMS) polymer has the general formula:

R1 - Si(CH3)2 - O - [- Si(CH3)2 - O -]x - Si(CH3)2 - R2

R1 = hydrogen, methyl, methoxy, ethoxy, hydroxy, propoxy, and aryloxy group. R2 = hydrogen, methyl, methoxy, ethoxy, hydroxy, propoxy, and aryloxy group. A suitable example of a PDMS polymer is E22 ex. Wacker Chemie.

Most preferably the silicone is a carboxy functionalised silicone as described above.

The molecular weight of the silicone polymer is preferably from 1 ,000 to 500,000, more preferably from 2,000 to 250,000 even more preferably from 5,000 to 200,000.

The silicone of the present invention is preferably present in the form of an emulsion. Silicones are preferably emulsified prior to addition to the present compositions. Silicone compositions are generally supplied from manufacturers in the form of emulsions.

The dispersed droplets of silicone may generally have a volume average primary particle size in the range from about 1 nm to 100 microns, including microemulsions (< 150 nm), standard emulsions (about 200 nm to about 500 nm) and macroemulsions (> 1 micron). Preferably the volume average primary particle size is in the range from about 10 nm to about 1 microns. The volume average primary particle size can be measured using a Coulter particle size analyser™.

Product Form The benefit agent delivery particles of the invention are suitable for incorporation into laundry treatment compositions of all physical forms. Laundry treatment compositions according to the invention may be in any suitable form.

Preferably the benefit agent delivery particles are present in the 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 term 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.

Product Types

Preferably the laundry treatment composition according to the invention is a laundry detergent composition.

Examples of laundry detergents include detergents for use in the wash cycle of automatic washing machines or by hand.

A laundry detergent composition according to the invention generally comprises at least 3%, such as from 5 to 90% (by weight based on the total weight of the composition) of one or more detersive surfactants. The choice of 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.

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. Non-soap anionic surfactants for use in the invention are typically 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. Examples of such materials include alkyl sulfates, alkyl ether sulfates, alkaryl sulfonates, alphaolefin 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) diethanolamine (DEA) or triethanolamine (TEA). Mixtures of such counterions may also be employed.

A highly preferred class of non-soap anionic surfactant for use in the invention includes alkylbenzene sulfonates, particularly linear alkylbenzene sulfonates (LAS) with an alkyl chain length of from 10 to 18 carbon atoms. LAS is particularly effective as a surfactant. LAS and certain benefit agents, in particular certain oils such as ester oils are incompatible in liquid/gel formulations however, with the encapsulation arrangement of the invention, a LAS-rich laundry liquids ( where LAS is incorporated above 5wt%, preferably above 7wt% of the total composition) with fabric care benefits can be formulated.

Commercial 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 11 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. LAS is normally formulated into compositions in acid (i.e. HLAS) form and then at least partially neutralized in-situ.

Also suitable are 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.

Some alkyl sulfate surfactant (PAS) may be used, such as non-ethoxylated primary and secondary alkyl sulphates with an alkyl chain length of from 10 to 18.

Mixtures of any of the above described materials may also be used. A preferred mixture of non-soap anionic surfactants for use in the invention comprises linear alkylbenzene sulfonate (preferably Cn to C15 linear alkyl benzene sulfonate) and sodium lauryl ether sulfate (preferably C10 to C alkyl sulfate ethoxylated with an average of 1 to 3 EO).

In a laundry detergent according to the invention, 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. Within the block structures, 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 Cs 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 Cis 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 G , 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.

Mixtures of any of the above described materials may also be used.

In a laundry detergent according to the invention, the total level of nonionic surfactant may suitably range from 0 to 25% (by weight based on the total weight of the composition).

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 nonaqueous 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).

Mixtures of any of the above described materials may also be used.

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).

Builders

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.

Preferably 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 (phyllosilicates) of the general formula (I)

NaMSi _x O2x+i.yH ₂ O (I) in which M is sodium or hydrogen, x is a number from 1.9 to 4, preferably 2 or 3 and 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, p, y and 5 phases, with b-sodium disilicate being most preferred. Zeolites are naturally occurring or synthetic crystalline aluminosilicates composed of (SiC ) ⁴ ' and (AIC ) ⁵ ' tetrahedra, which share oxygen-bridging vertices and form cage-like structures in crystalline form. The ratio between oxygen, aluminium and silicon is O:(AI + Si) = 2:1. 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): Na _x [(AIO2)x(SiO ₂ )y] zH ₂ O (II) in which 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, b-sodium disilicate and mixtures thereof.

Suitable organic, non-phosphate builders for use in the invention include polycarboxylates, 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 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 ethylenediaminetetraacetates, sodium and potassium N(2-hydroxyethyl)-ethylenediamine triacetates, sodium and potassium nitrilotriacetates and sodium and potassium N-(2- hydroxyethyl)-nitrilodiacetates. 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). Specific examples of 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.

Mixtures of any of the above described materials may also be used.

Preferably 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). The term “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).

Polymeric cleaning boosters

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 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 carboxymethyl cellulose.

Mixtures of any of the above described materials may also be used.

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. Examples of such materials include 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

Other types of SRP for use in the invention include cellulosic derivatives such as hydroxyether cellulosic polymers, C1-C4 alkylcelluloses and C4 hydroxyalkyl celluloses; polymers with poly(vinyl ester) hydrophobic segments such as graft copolymers of poly(vinyl ester), for example Ci-Ce vinyl esters (such as poly(vinyl acetate)) grafted onto polyalkylene oxide backbones; poly(vinyl caprolactam) and related co-polymers with monomers such as vinyl pyrrolidone and/or dimethylaminoethyl methacrylate; and polyester-polyamide polymers prepared by condensing adipic acid, caprolactam, and polyethylene glycol.

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): in which R ¹ and R ² independently of one another are X-(OC2H4)n-(OC3H6)m _; in which X is C1.4 alkyl and preferably methyl; n is a number from 12 to 120, preferably from 40 to 50; m is a number from 1 to 10, preferably from 1 to 7; and 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.

Mixtures of any of the above described materials may also be used. 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).

Fatty Acid

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.

Mixtures of any of the above described materials may also be used.

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).

For formula accounting purposes, in the formulation, fatty acids and/or their salts (as defined above) are not included in the level of surfactant or in the level of builder.

Rheology modifiers

A liquid laundry detergent according to the invention may comprise one or more rheology modifiers. Examples of such materials 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 polyoxyalkylene section between the ethylenically unsaturated section and the hydrophobic section. 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.

Mixtures of any of the above described materials may also be used.

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. Examples of such materials 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.

Enzymes

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.

Fragrances

Examples of 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.

Further Optional Ingredients

A laundry treatment composition of the invention may contain further optional ingredients to enhance performance and/or consumer acceptability. Examples of such ingredients including fragrances either as free oil or encapsulated (in addition to the encapsulates of the invention), foam boosting agents, preservatives (e.g. bactericides), antioxidants, sunscreens, anticorrosion agents, colorants, pearlisers and/or opacifiers, and shading dye. Each of these ingredients will be present in an amount effective to accomplish its purpose. Generally, these optional ingredients are included individually at an amount of up to 5% (by weight based on the total weight of the composition).

Packaging and dosing

A laundry treatment composition of the invention may be packaged as unit doses in polymeric film soluble in the wash water. Alternatively, 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 treatment liquor e.g. a wash liquor, and treating fabrics with the liquor so formed. The method may be carried out in an automatic washing machine, or can be carried out by hand. The method may include the step of immersing the fabrics in the liquor, or applying the liquor or the (undiluted) composition to the fabrics.

In automatic washing machines, 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. Alternatively, 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. 50 ml or less) may be used for hand washing methods (using about 1 to 10 litres of water to form the wash liquor). A subsequent aqueous rinse step and drying the laundry is preferred. 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.

The invention will now be further described with reference to the following non-limiting Examples.

EXAMPLES

All weight percentages are by weight based on total weight unless otherwise specified.

Example 1 - Synthesis of PCL Shell and Silicone Encapsulates

Polycaprolactone shell silicone encapsulates were synthesised using the following method. The materials used in the encapsulation are given in the following table:

A 1 wt% xyloglucan aqueous stock solution was prepared by dissolving 1g of xyloglucan (Glyloid 3S) into 99g of boiled water by homogenising for 5 minutes at 8,000rpm.

A 4wt% polyvinyl alcohol stock solution was made by adding 20g Mowiol 4-88 slowly into boiled water with vigorous overhead stirring.

An oil phase was prepared by dissolving 5.1g of polycaprolactone and11.9g of silicone oil in 50ml dichloromethane. This mixture was agitated overnight to achieve dissolution.

An aqueous phase was prepared by mixing 61 ,0g of the 4 wt% polyvinyl alcohol stock with 34.0g of the 1 wt% xyloglucan stock solution. The oil and aqueous phases were mixed and homogenised for 2 minutes at 12,000 rpm to generate an O/W emulsion. This was transferred to a rotary evaporator flask and the organic solvent (dichloromethane) removed by rotary evaporation, at room temperature, by gradual reduction of the pressure to 200 mbar over approximately 2 hours.

A final encapsulate dispersion (112g) consisting of 20.4 wt% encapsulate solids (determined at 50°C), composed of a polycaprolactone shell and silicone oil core (30/70 respectively), containing 2 wt% (on final encapsulate weight) of non-chemically grafted xyloglucan was obtained. The particle size was approximately 5 microns.

Example 2 - Chemical Grafting of Xyloglucan to Polycaprolactone Silicone Encapsulates

A fresh aqueous solution of coupling agent was prepared by dissolving 0.1g of 1 -ethyl-3- (3'-dimethylaminopropyl)carbodiimide, HCI salt (Aldrich) in 0.9g deionised water. This solution was used within 15 minutes. 0.27ml of this solution was added to 20ml of the encapsulate dispersion described above (PCL-Silicone encapsulates). This mixture was agitated overnight to facilitate chemical grafting of the xyloglucan to the encapsulate.

The final dispersion had a measured solids (determined at 50°C) of 19.2% and size of approximately 5 microns.

Example 3 - Synthesis of Polycaprolactone Shell and Ester Oil Core Encapsulates

Materials

Polycaprolactone shell and ester oil encapsulates were synthesised using the following method. The materials used in the encapsulation are given in the following table:

A 1 wt% xyloglucan aqueous stock solution was prepared by dissolving 1g of xyloglucan (Glyloid 3S) into 99g of boiled water by homogenising for 5 minutes at 8,000rpm.

A 4 wt% polyvinyl alcohol stock solution was made by adding 20g Mowiol 4-88 slowly into boiled water with vigorous overhead stirring.

An oil phase was prepared by dissolving 5.1g of polycaprolactone, 11.9g of Priolube 3987 and 0.0024g of Hostasol Yellow 3G in 50ml of dichloromethane. This mixture was agitated overnight to achieve dissolution.

An aqueous phase was prepared by mixing 61 ,0g of the 4 wt% polyvinyl alcohol stock with 34.0g of the 1 wt% xyloglucan stock solution.

The oil and aqueous phases were mixed and homogenised for 2 minutes at 12,000 rpm to generate an oil/water. This was transferred to a rotary evaporator flask and the organic solvent (dichloromethane) removed by rotary evaporation, at room temperature, by gradual reduction of the pressure to 200 mbar over approximately 2 hours.

A final encapsulate dispersion (112g) consisting of 18.0 wt% encapsulate solids (determined at 50°C), composed of a polycaprolactone shell and ester oil core (30/70 respectively), containing 2 wt% (on final encapsulate weight) of non-chemically grafted xyloglucan was obtained. The particle size was approximately 3 microns. Example 4 Chemical Grafting of Xyloglucan to Polycaprolactone Shell and Ester Oil Core Benign Encapsulates

Various levels of coupling agent (0.65-10.0% on encapsulate weight) were assessed to maximise and optimise level of coupling agent. A fresh aqueous solution of coupling agent was prepared by dissolving 0.2g of 1 -ethyl-3- (3'-dimethylaminopropyl)carbodiimide, HCI salt (Aldrich) in 1.8g deionised water. This solution was used within 15 minutes. A set of 5 materials were prepared by adding 0.06, 0.09, 0.27, 0.45 and 0.90ml of this solution to 5ml of the encapsulate dispersion described above (polycaprolactone shell and ester oil core benign encapsulates). These mixtures were agitated overnight to facilitate chemical grafting (covalent bonding) of the xyloglucan to the encapsulate shells.

The final dispersions obtained were as follows: *The grafting efficiency was determined by creaming the encapsulates by centrifugation (1 hr at 11 ,000rpm) and the supernatant liquor underneath was sampled (using a glass pipette). This fraction contained any ungrafted xyloglucan and this level was determined by GPC (Malvern Omnisec equipped with an A600M and A7000 columns) via extrapolation of a calibration plot. From this, by mass balance with the initial level added, the grafted level can be determined.

The onset of inter-particle aggregation is around 5 wt% (on encapsulate weight) of coupling agent, reflected in d(0.9) increase, an optimum level of 3% results in achieving maximum grafting efficiency whilst mitigating aggregates.

Zeta potential fall can also be used as efficiency indicator of high grafting, with the optimum target value being zero.

Example 5 - Deposition Testing

To six Linitest pots, were added 100mls of demin water and 0.26g of a liquid detergent product as follows:

PCL- ester oil encapsulates were introduced to the pots as follows: To each of three of the pots, 250ppm (based on slurry solids) polycaprolactone (PCL) encapsulates (from Example 3) was added. To each of the remaining three pots, 250ppm of Xyloglucan-modified (grafted) polycaprolactone encapsulates (Example 4) were added. All pots were then agitated to ensure mixing.

Out of each of these pots a 5ul aliquot was taken and saved for measurement later. A 20x20cm piece of unfluoresced cotton was added to each pot and the pots all sealed. These were then clamped into the Linitest/Rotawasher. The Linitest is a laboratory scale washing machine (Ex. Heraeus). The equipment is designed and built to comply with the requirements for international standard test specifications. It is used for small scale detergency and stain removal testing particularly when low liquor to cloth ratios are required.

There are various models of the Linitest commercially available. The model used in this case has a single rotation speed of 40 rpm. The carrier can accommodate twelve 500ml steel containers and can be operated at temperatures up to 100°C.

The Linitest comprises a 20-litre tank, control system and drive mechanism. Permanent thermostatically controlled tubular heating elements in the base of the tank heat the bath liquor to the required temperature. The stainless-steel construction throughout ensures efficient heat transfer to the specimen containers that are mounted on a rotating horizontal carrier driven by a geared motor. The rotating movement of the carrier 'throws' the liquid from one end of the container to the other in a continuous action. This movement simulates the mechanical washing process and additional mechanical action can be obtained by using steel ball bearings or discs.

The Linitest pots were attached to the Linitest cradle and rotated 45 minutes at 30°C to simulate the main wash. The cloths were then removed and wrung by hand and a 5ml aliquot of the remaining wash liquor was taken. The Linitest pots were then thoroughly rinsed and the 'wrung' cloths returned to the pots and 100ml of de-ionised water was added. The pots were re-attached to the cradle and rotated for 10 minutes again at the same temperature 30°C to simulate a rinse procedure. The clothes were then removed and wrung by hand. A 5ml aliquot of the rinse solution was also taken from each pot. With these 3 samples deposition could be measured for sample 1 and sample 2 via fluorescence spectroscopy measurement of the Hostasol in the particles. Hostasol has an excitation around 450nm and an emission around 510nm. Measurement of the aliquots at these wavelengths provides three values that can be used to calculate deposition of the encapsulates.

The results show that ester oils can be effectively encapsulated in polyester shells and that the oil deposits effectively to fabric when in a laundry liquid detergent composition comprising anionic surfactants, even in high LAS (above 5%wt - based on total wt of formulation) formulations, and this is further improved by the presence of xyloglucan.