POLYMER SHELL MICROCAPSULES WITH DEPOSITION POLYMER

Abstract

A microcapsule containing a benefit agent inside a polyurea shell characterised in that polyurea has a nonionic polysaccharide deposition polymer covalently bonded to it. Also a process for making the microcapsule and compositions incorporating the microcapsule.

Claims

1. A microcapsule containing a benefit agent inside a polyurea shell characterised in that the polyurea has a nonionic polysaccharide deposition polymer covalently bonded to it.

2. A microcapsule according to claim 1 in which the deposition polymer is a nonionic polysaccharide selected from the group consisting of mannan, glucan, glucomannan, xyloglucan, hydroxyalkyl cellulose, dextran, galactomannan and mixtures thereof.

3. A microcapsule according to claim 2 in which the deposition polymer is selected from the group consisting of xyloglucan, galactomannan, dextran and hydroxypropyl cellulose.

4. A microcapsule according to claim 3 in which the deposition polymer is xyloglucan or hydroxypropyl cellulose.

5. A microcapsule according to any preceding claim in which the weight ratio of deposition polymer to polyurea shell lies in the range 1:500 to 1:2.

6. A microcapsule according to any preceding claim in which the nonionic polysaccharides have a molecular weight Mw in excess of 40 kDa.

7. A microcapsule according to any preceding claim comprising from 1 to 30 wt % polyurea shell.

8. A microcapsule according to any preceding claim in which the deposition polymer levels are from 0.1 to 10 wt %, based on microcapsule weight.

9. A microcapsule according to any preceding claim in which the polyurea is formed by the reaction of poly-isocyanate and diamine.

10. A composition including at least 0.01 wt % of the microcapsules as claimed in any one of claims 1 to 9 and a surfactant or cationic material.

11. A laundry detergent composition according to claim 10 comprising at least 5 wt % anionic surfactant.

12. A skin cleansing composition or hair shampoo composition according to claim 10 comprising at least 2 wt % surfactant.

13. A hair conditioner composition according to claim 10 comprising at least 1 wt % cationic material.

14. A composition according to any one of claims 10 to 13 further comprising at least 0.1 wt % perfume.

15. A method of making the microcapsule of any one of claims 1 to 9 wherein the nonionic polysaccharide is added at least 15 minutes after commencement of curing of the polyurea.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0024] The nonionic polysaccharide deposition polymer

[0025] Preferred nonionic polysaccharide deposition polymers may be selected from the group consisting of: tamarind gum (preferably consisting of xyloglucan polymers), guar gum, locust bean gum (preferably consisting of galactomannan polymers), and other industrial gums and polymers, which include, but are not limited to, Tara, Fenugreek, Aloe, Chia, Flaxseed, Psyllium seed, quince seed, xanthan, gellan, welan, rhamsan, dextran, curdlan, pullulan, scleroglucan, schizophyllan, chitin, hydroxyalkyl cellulose, arabinan (preferably from sugar beets), de-branched arabinan (preferably from sugar beets), arabinoxylan (preferably from rye and wheat flour), galactan (preferably from lupin and potatoes), pectic galactan (preferably from potatoes), galactomannan (preferably from carob, and including both low and high viscosities), glucomannan, lichenan (preferably from icelandic moss), mannan (preferably from ivory nuts), pachyman, rhamnogalacturonan, acacia gum, agar, alginates, carrageenan, chitosan, clavan, hyaluronic acid, heparin, inulin, cellodextrins, cellulose, cellulose derivatives and mixtures thereof.

[0026] Non-hydrolysable nonionic polysaccharides are most preferred. The polysaccharide preferably has a -1,4-linked backbone. However, dextran which does not have such a backbone, is also preferred.

[0027] Preferably the polysaccharide is a cellulose, a cellulose derivative, or another -1,4-linked polysaccharide having an affinity for cellulose, preferably mannan, glucan, glucomannan, xyloglucan, galactomannan and mixtures thereof. More preferably, the polysaccharide is selected from the group consisting of xyloglucan and hydroxypropyl cellulose. Galactomannan is typically from Locust bean gum and/or guar.

[0028] A highly preferred nonionic polysaccharide is Hydroxypropyl Cellulose with a molecular weight in excess of 40 kDa. Hydroxypropyl Cellulose (HPC) has the repeat structure shown in generalised terms below:

##STR00001##

[0029] Especially good results may be obtained when the HPC is one with a viscosity in 2 wt % aqueous solution of 1000 to 4000 mPa.Math.s. Viscosity measurements are done using a Brookfield viscometer, Spindle #3, @30 rpm. Lower viscosity materials are measured using Spindle #2, @60 rpm.

[0030] HPC is an ether of cellulose in which some of the hydroxyl groups in the repeating glucose units have been hydroxy-propylated forming OCH.sub.2CH(OH)CH.sub.3 groups using propylene oxide. The average number of substituted hydroxyl groups per glucose unit is referred to as the degree of substitution (DS). Complete substitution would provide a DS of 3. However, as the hydroxy-propyl group itself contains a hydroxyl group, this can also be etherified during preparation of HPC. When this occurs, the number of moles of hydroxy-propyl groups per glucose ring, moles of substitution (MS), can be higher than 3.

[0031] The majority (typically around 75% for a DS of 3) of the mass of HPC is found in the substituent groups rather than the backbone.

[0032] Also, nonionic polysaccharides selected from the group consisting of: hydroxy-propyl methyl cellulose, hydroxy-ethyl methyl cellulose, hydroxy-propyl guar, hydroxy-ethyl ethyl cellulose and methyl cellulose may be used.

[0033] The ring spacing of these -1,4-linked polymers is such that each alternate ring of the polymer is well placed to allow a pseudo hydrogen-bond interaction with the pi-electron clouds of the phthalate rings in polyester. Moreover, these polymers have a balance of hydrophobicity and hydrophillicity which means that they are able to interact with a fabric without being so hydrophobic as to be insoluble. Other nonionic, modified polysaccharides, for example hydroxyl-ethyl cellulose, do not have the correct properties and show poor performance as deposition polymers, especially on polyester.

[0034] In those ethers of cellulosics in which some of the hydroxyl groups in the repeating glucose units have been hydroxy-alkylated the average number of substituted hydroxyl groups per glucose unit is referred to as the degree of substitution (DS). Complete substitution would provide a DS of 3. However, if the substituent group itself contains a hydroxyl group, this can also be etherified. When this occurs, the number of moles of substituent groups per glucose ring, moles of substitution (MS), can be higher than 3.

[0035] Some of the OH groups (where present) in the hydroxyl-alkyl pendant group may be replaced with alkyl ethers. Typically these are C.sub.1-C.sub.20 alkyl ethers, and may, in specific cases be C.sub.16-C.sub.22 ethers. The most preferred alkyl chain is stearyl.

[0036] Hydroxy-propyl methyl cellulose (HPMC), has the repeat structure shown in generalised terms below:

##STR00002##

[0037] Since the hydroxypropoxy substituents can be attached to each other on side chains, the degree of substitution for HPMC can be higher than 3.

[0038] In useful derivatives of HPMC Sangelose some of the OH groups in the hydroxyl-propyl pendant group are replaced with alkyl ethers. Typically these are C.sub.1-C.sub.20 alkyl ethers, and may, in specific cases be C.sub.16-C.sub.22 ethers. The most preferred alkyl chain is stearyl.

[0039] Hydroxy-ethyl methyl cellulose (HEMC), has the repeat structure shown in generalised terms below:

##STR00003##

[0040] Since the ethoxy substituents can be attached to each other on side chains, the degree of substitution can be higher than 3.

[0041] Hydroxy-propyl guar (HPG), has the repeat structure shown in generalised terms below:

##STR00004##

[0042] Since the hydroxypropoxy substituents can be attached to each other on side chains, the degree of substitution in HPG can be higher than 3.

[0043] Hydroxy-ethyl ethyl cellulose (HEEC), has the repeat structure shown in generalised terms below:

##STR00005##

[0044] HEEC is less preferred than other nonionic polysaccharide delivery aids disclosed herein.

[0045] Methyl cellulose (ME), has the repeat structure shown in generalised terms below:

##STR00006##

[0046] The theoretical maximum degree of substitution (DS) is 3.0. However, more typical values are 1.3 to 2.6.

[0047] Especially good results may be obtained when the deposition polymer is one which has a viscosity in 2 wt % aqueous solution of over 1000 mPa.Math.s. Viscosity measurements are made using a Brookfield viscometer, Spindle #3, @30 rpm. Lower viscosity materials are measured using Spindle #2, @60 rpm.

[0048] Preferably the nonionic polysaccharide deposition polymer has a molecular weight above 50 kDa and more preferably above 140 kDa, most preferably above 500 kDa. As the molecular weight is increased the performance of the deposition polymer generally increases.

[0049] DS is typically in the range from 1.0 to 3, more preferably above 1.5 to 3, most preferably, where possible from 2.0 to 3.0.

[0050] A typical MS for the deposition polymer is 1.5 to 6.5. Preferably the MS is in the range from 2.8 to 4.0, more preferably above 3.0, most preferably from 3.2 to 3.8.

[0051] Preferably, the deposition-aid polymer is present at levels such that the ratio, polymer: particle solids, is in the range 1:500 to 3:1, more preferably 1:500 to 1:2 and most, preferably 1:200 to 1:2.

The Polyurea

[0052] Polyureas are formed from diisocyanates or polyisocyanates with diamines or polyamines. Normally to make a microcapsule the cyanate part is present in a dispersed (oily) phase and the amine part is present in the continuous (aqueous) phase. The shell forms via interfacial polymerisation at the phase interface. This reaction and the manufacture of polyurea shell microcapsules is widely known and understood to the skilled person and the invention can be applied to any type of polyurea microcapsule.

[0053] When a diisocyanate is used it may be linear aliphatic, cycloaliphatic or aromatic.

[0054] Suitable, aromatic polyisocyanates comprise, but are not limited to, 2,4- and 2,6-toluene diisocyanate, naphthalene diisocyanate, diphenyl methane diisocyanate and triphenyl methane-p,pp-trityl triisocyanate, polymethylene polyphenylene isocyanate, 2,4,4-diphenylether triisocyanate, 3,3-dimethyl-4,4-diphenyl diisocyanate, 3,3-dimethoxy-4,4diphenyl diisocyanate, and 4,44-triphenylmethane triisocyanate.

[0055] Suitable aliphatic polyisocyanates comprise, but are not limited to dicyclohexylmethane 4,4-diisocyanate, hexamethylene-1,6-diisocyanate, isophorone diisocyanate, trimethyl-hexamethylene diisocyanate, trimer of hexamethylenel,6-diisocyanate, trimer of isophorone diisocyanate, 1,4-cyclohexane diisocyanate, urea of hexamethylene diisocyanate, trimethylene diisocyanate, propylene-1,2-diisocyanate and butylenes-1,2-diisocyanate and mixtures thereof.

[0056] Suitable diamines can comprise amines such as ethylene diamine (EDA), phenylene diamine, toluene diamine, hexamethylene diamine, diethylenetriamine, tetraethylene pentaamine, pentamethylene hexamine, 1,6-hexane diamine, Methylene tetramine, 2,4-diamino-6-methyl-1,3,5 triazine 1,2-diaminocyclohexane, 4,4-diamino-diphenylmethane, 1,5-diaminonaphthalene, 2,4,4-triaminodiphenylether, bis(hexa-methylenetriamine), 1,4,5,8-tetraaminoanthraquinone, isophorone diamine, diamino propane and diaminobutane, and mixtures thereof. Polymeric amines may also be used, for example Jeffamines (polyether amine) and poly(ethyleneimine).

[0057] Water soluble diamine or amine salt or polyamines or polyamines salts are preferred as the amine is usually present in the aqueous phase. Combinations of Polyisocyanates and diamines are preferred because the plural functionality enables networked structures and having the plural functional material in the disperse phase reduces the chance of bonds forming between adjacent particles and clumping resulting

[0058] Other suitable materials are disclosed, for example, in US2014/0017287. Isocyanate-based capsule wall technologies are also disclosed in WO 2004/054362; EP 0 148149; EP 0 017 409; U.S. Pat. No. 4,417,916, U.S. Pat. No. 4,124,526, U.S. Pat. No. 6,566,306, U.S. Pat. No. 6,730,635, WO 90/08468, WO 92/13450, U.S. Pat. No. 4,681,806, U.S. Pat. No. 4,285,720, U.S. Pat. No. 6,340,653 and EP 2673078.

The Benefit Agent

[0059] A benefit agent is a material that when deposited onto a substrate imparts some desirable effect to that substrate. As such it comprises a wide selection of materials. Because polyurea capsules are made by interfacial polymerisation from an oil in water emulsion the benefit agent is generally a hydrophobic material that is miscible with an oil phase or forms the oil phase.

[0060] Suitable benefit agents include perfume raw materials (also referred to herein as fragrance), silicone oils, waxes, hydrocarbons, higher fatty acids, essential oils, lipids, skin coolants, vitamins, sunscreens, antioxidants, malodour reducing agents, odour controlling materials, skin softening agents, insect and moth repelling agents, colorants, chelants, sanitization agents, germ control agents, skin care agents, natural actives, antibacterial actives, preservatives, chemosensates, (for example menthol), sunless-tanning agents (for example dihydroxyacetone), emollients (for example sunflower oil and petrolatum), antiaging agents, anti-inflammatory agents, skin conditioning agents, skin lightening agents and mixtures thereof.

[0061] Preferred benefit agents are fragrance, anti-aging agents, antimicrobial agents, anti-bacterial agents, anti-fungal agents, lubricants and shading dyes. Other possible benefit agents include: anti-oxidants, vitamins, anti-inflammatory actives, skin lightening agents, skin conditioning agents, for example 12-hydroxy stearic acid, oils, insect repellents and sunscreens. These are described in detail in the literature. For example: WO13/026657 and WO12/022736.

Optional Materials in the Microcapsule (Including Wall)

[0062] Isocyanate must be soluble in whatever will form the microcapsule core so additional material may be needed if the benefit agent does not dissolve the isocyanate.

[0063] The microcapsule may therefore optionally comprise a carrier oil (also referred to herein as a diluent). It will be clear to a skilled person which oils are suitable for use with a certain benefit composition. The carrier oils are hydrophobic materials that are miscible in the benefit agent materials used in the present invention. Suitable oils are those having reasonable affinity for the benefit agent. Suitable materials include, but are not limited to triglyceride oil, mono and diglycerides, mineral oil, silicone oil, diethyl phthalate, polyalpha olefins, castor oil and isopropyl myristate. Preferably, the oil is a triglyceride oil, most preferably a capric/caprylic triglyceride oil.

[0064] Many emulsifying agents are known for use in emulsion polymerisation. Suitable emulsifying agents for use in the polymerisation process may comprise, but are not limited to, nonionic surfactants such as polyvinylpyrrolidone (PVP), polyethylene glycol sorbitan monolaurate (Tween 20), polyethylene glycol sorbitan monopalmitate (Tween 40), polyethylene glycol sorbitan monooleate (Tween 80), polyvinyl alcohol (PVA), and poly(ethoxy)nonyl phenol, ethylene maleic anhydride (EMA) copolymer, Easy-Sperse (from ISP Technologies Inc.), ionic surfactants such as partially neutralized salts of polyacrylic acids such as sodium or potassium polyacrylate or sodium or potassium polymethacrylate. Brij-35, Hypermer A 60, or sodium lignosulphate, and mixtures thereof.

[0065] Emulsifiers may also include, but are not limited to, acrylic acid-alkyl acrylate copolymer, poly(acrylic acid), polyoxyalkylene sorbitan fatty esters, polyalkylene co-carboxy anhydrides, polyalkylene co-maleic anhydrides, poly(methyl vinyl ether-co-maleic anhydride), poly(propylene-co-maleic anhydride), poly(butadiene co-maleic anhydride), and poly(vinyl acetate-co-maleic anhydride), polyvinyl alcohols, polyalkylene glycols, polyoxyalkylene glycols, and mixtures thereof.

[0066] Preferred emulsifying agents are fatty alcohol ethoxylates (particularly of the Brij class), salts of ether sulphates (including SLES), alkyl and alkaryl sulphonates and sulphates (including LAS and SDS) and cationic quaternary salts (including CTAC and CTAB).

[0067] Typically a co-surfactant will be present in the dispersed phase and in the resulting particle. Suitable co-surfactants for use in the present invention include hexadecane, cetyl alcohol, lauroyl peroxide, n-dodecyl mercaptan, dodecyl methacrylate, stearyl methacrylate, polystyrene, polydecene, mineral oils, isopropyl myristate, C.sub.12-C.sub.15 alkyl benzoate and polymethyl methacrylate.

[0068] The preferred cosurfactants comprise hexadecane, polydecene and isopropyl myristate.

[0069] As a wt % of oil phase as a total, the co-surfactant is typically 0 to 20 wt %, preferably 1 to 15 wt %, more preferably 2 to 12.5 wt %.

[0070] In the prior art it has been suggested that pure polyurea shell walls are not useful due to their inherent leakiness. Inclusion of materials such as Carboxymethyl cellulose into the wall is taught as are more complex shell walls made of mixtures of polyurea and other polymers. In the present invention it is advantageous for the capsule wall to be at least 95% and preferably substantially 100% polyurea. Capsule leakiness can be adjusted by wall thickness and choice of the amine(s) and isocyanate(s). For some applications, e.g. laundry, it is desirable that some benefit agent leaks from the capsule before it ruptures. When the benefit agent is a perfume this can increase freshness perception when the washing is still wet.

Size of Microcapsule

[0071] Generally, the microcapsules will have an average diameter of from about 0.001 to about 1,000 microns, preferably from about 1 to about 500 microns, more preferably from about 5 to about 100 microns, and even more preferably from about 10 to about 50 microns. These dimensions can play an important role in the ability to control the application of the microcapsule composition in the practice of the present invention. The broadest range of microcapsule size under any conditions would be about 0.001 to about 1,000 microns and a more easily sprayed size limit would be between about 10 and about 50 microns.

[0072] It is desirable for a suspension of microcapsules to contain a dispersant also in order to prevent microbial contamination it is desirable that the microcapsule composition contains a preservative. The preservative may be contained in the core material and/or in the aqueous carrier.

Uses of the Microcapsules and Suitable Compositions

[0073] The compositions for use in the invention may contain one or more other ingredients in addition to the polyurea microcapsules with nonionic polysaccharide deposition polymer. They may contain other types of microcapsules or similar microcapsules with a different benefit agent inside.

[0074] In addition to any fragrance formulation that may be contained within the microcapsules, a composition comprising microcapsules of the present invention may also contain free perfume.

[0075] Formulated compositions comprising the particles of the invention may contain a surface-active compound (surfactant) which may be chosen from soap and non-soap anionic, cationic, nonionic, amphoteric and zwitterionic surface active compounds and mixtures thereof. Many suitable surface active compounds are available and are fully described in the literature, for example, in Surface-Active Agents and Detergents, Volumes I and II, by Schwartz, Perry and Berch. The preferred surface-active compounds that can be used are soaps and synthetic non soap anionic, and nonionic compounds. Depending on the end use of the composition comprising the microcapsules other materials commonly found in such compositions may be used as usual. The one main exception is that free cellulase is preferably absent from the composition unless it is somehow deactivated. Mannanase is also desirably avoided.

[0076] Such ingredients include preservatives (e.g. bactericides), pH buffering agents, perfume carriers, anti-redeposition agents, soil-release agents, polyelectrolytes, anti-shrinking agents, anti-wrinkle agents, anti-oxidants, sunscreens, anti-corrosion agents, drape imparting agents, anti-static agents, pearlisers and/or opacifiers, natural oils/extracts, processing aids, e.g. electrolytes, hygiene agents, e.g. anti-bacterials and antifungals, thickeners, skin benefit agents, colorants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly peroxide compounds and active chlorine releasing compounds), gel-control agents, freeze-thaw stabilisers, bactericides, preservatives (for example 1,2-benzisothiazolin-3-one), hydrotropes, perfumes and mixtures thereof.

[0077] The compositions for use in the invention may also contain pH modifiers such as hydrochloric acid or lactic acid.

[0078] The end-product compositions of the invention may be in any suitable physical form e.g. a solid such as a solid bar, a paste; or a liquid or gel, preferably, an aqueous-based liquid.

[0079] Laundry detergents, skin cleansing compositions and hair conditioners are preferred compositions for use with the microcapsules.

[0080] The microcapsules are typically included in compositions at levels of from 0.01% to 10%, preferably from 0.5% to 7%, most preferably from 0.5% to 5% by weight of the total composition.

[0081] The invention will now be further described with reference to the following non-limiting examples.

EXAMPLES

Example 1Synthesis of Polyurea Microcapsule with Xyloglucan Added at Various Addition Times

[0082] A number of polyurea microcapsules were synthesised, whereby the xyloglucan deposition polymer was added over various addition times, once the encapsulating process had begun. The materials sued are given in Table 1 and composition details are given in Table 2.

TABLE-US-00001 TABLE 1 Material Supplier % Active Benzyl Acetate Aldrich >99% Hostasol Yellow 3G Clariant 100% Poly(methylene(polyphenyl)isocyanate) Polysciences 100% Active (30% Isocyanate) LAS (Linear Alkyl Benzene Petrelabs 90% Sulphonate, Sodium Salt) Hexamethylene Diamine Aldrich 98% Xyloglucan DSP Gokyo 100% Food and Chem. Co.

TABLE-US-00002 TABLE 2 Particle Solids (%) = 15 % BA (on solids) = 89.6 % Hostasol (on oil phase) = 0.02 % PMPHI (on solids) = 7.2 % HMDA (on solids) = 3.2 Total Wt (g) = 200 % XG (on solids) = 2.0

[0083] The microcapsules were made using the following synthesis: [0084] 1) 0.0054 g of Hostasol yellow 3G and 2.2 g of poly(methylene(polyphenyl)isocyanate) were dissolved in 26.9 g of benzyl acetate (oil phase). [0085] 2) 0.77 g of LAS (linear alkyl benzene sulfonate) was dissolved in 100 ml of deionised water by stirring for 30 minutes (aqueous phase). [0086] 3) A 1 wt % xyloglucan (XG) solution was prepared separately by homogenising (8,000 rpm) 5 g XG in 495 g of boiled distilled water for 5 minutes and allowing to cool before use. [0087] 4) The oil and aqueous phases were mixed and emulsified using a homogeniser (5,000 rpm) for 2 minutes (care was taken to avoid excessive foaming). [0088] 5) This mixture was constantly stirred using an overhead stirrer (200 rpm). [0089] 6) The water for solids adjustment was added (64.2 g for XG free sample and 4.2 g for all XG containing samples). [0090] 7) Then 0.96 g hexamethylene diamine dissolved in 5 g of deionised water was added dropwise. [0091] 8) Numerous samples were prepared, one where no XG solution was added (control) and the others whereby 60 g of the 1 wt % XG solution was added after 7, 15, 30, 45 or 60 minutes. [0092] 9) Polyurea curing was allowed to proceed at room temperature for at least 3 hours.

Example 2Deposition Assessment Via Fluorescence Depletion

1) Preparation of Wash Liquor Stock Solutions

[0093] A concentrated wash liquor stock solution (10) was prepared using the materials in Table 3.

TABLE-US-00003 TABLE 3 Component Active (%) Amount (g) LAS (Linear Alkyl Benzene Sulphonate, 90.0% 5.5 Sodium Salt) Neodol 25-7 100.0% 5.0 Na2CO.sub.3 100.0% 7.55 NaHCO.sub.3 100.0% 2.42 Deionised water N/A 979.5

2) Preparation of the Wash Liquor:

[0094] The wash liquor stock (10 ml) and deinonised water (90 ml) were added to a 125 ml plastic bottle. This gave 100 ml of wash liquor buffered to pH 10.5 and containing 1 g/L surfactant (50:50 LAS:Neodol 25-7).

3) Simulated Wash:

[0095] 0.005 g (50 ppm on wash liquor) of microcapsule particles were added to the plastic bottle containing wash liquor and agitated slightly to ensure mixing. (Washes were done in duplicate for each sample and results averaged). A 5 ml aliquot was taken from each and the fluorescence (excitation=450 nm, emission=515, slit width=15) measured in a 1 cm cuvette using a fluorimeter (Perkin Elmer LS50). This fluorescence value represents 100% particles in the wash solution prior to the simulated wash process.

[0096] A section of unfluoresced cotton measuring 20 cm by 20 cm was placed into each plastic bottle containing the wash liquor and microcapsules and the bottle sealed.

[0097] The bottles were agitated at 40 C. and 150 rpm using a water shaker bath (Haake SWB25) for 45 minutes to simulate the main wash.

[0098] The cloths were then removed and wrung by hand and a 5 ml aliquot of the remaining wash liquor was taken and the fluorescence measured (as before). From interpolation of a concentration versus florescence calibration curve, the concentration of the microcapsules remaining in the liquor after the wash could be determined and hence the percentage deposited (wash deposition) on cloth determined by difference.

[0099] The plastic bottles were then thoroughly rinsed and the wrung cloths returned to the bottles and 100 ml of de-ionised water was added and the bottles sealed. The bottles were then agitated (150 rpm) on the water shaker bath for 10 minutes at ambient temperature (20 C.) to simulate a rinse procedure. The clothes were then removed and wrung by hand. A 5 ml aliquot of the rinse solution was taken and the fluorescence determined as before. Again, interpolation of the calibration plot allowed the microcapsule concentration removed from the cloth during the rinse to be determined and, by subtraction from the level deposited after the main wash, the overall percentage deposition was determined.

[0100] The percentage depositions (after main wash and rinse) for the samples prepared in Example 1) are shown in Table 4.

TABLE-US-00004 TABLE 4 Main Wash After Rinse Polyurea - XG Addition Time Depo (%) SD Depo (%) SD Control (No XG) 58.4 5.0 44.5 5.6 After 7 mins 69.9 5.3 46.4 13.2 After 15 mins 83.1 3.0 72.6 0.1 After 30 mins 79.9 1.9 69.5 3.1 After 45 mins 86.3 4.4 73.3 1.2 After 60 mins 85.3 1.1 69.0 2.8

[0101] The results show that deposition is enhanced by the attachment of xyloglucan and that for maximum deposition, the xyloglucan should not be added until 15 minutes into the reaction. After this time, addition up to one hour is possible without detriment to deposition performance.

Example 3Synthesis of Comparative Melamine Formaldehyde Microcapsule

[0102] A comparative example prepared at equivalent composition levels and a xyloglucan addition time point of 15 minutes into microcapsule formation was prepared, with the difference that melamine formaldehyde was used as shell material (rather than polyurea) and the reaction was carried out at 75 C. for 3 hours. The composition details are given in Table 5 and the materials used in Table 6.

TABLE-US-00005 TABLE 5 Particle Solids (%) 15.0 Benzyl Acetate (% on solids) 89.6 Hostasol (% on oil phase) 0.02 Melamine Formaldehyde (% on solids) 10.4 Xyloglucan (% on solids) 2.0 Total Weight (g) 200

TABLE-US-00006 TABLE 6 Material Supplier % Active Melamine Aldrich 100% Formaldehyde Solution (Formalin) Aldrich 37.0% Benzyl Acetate Aldrich >99% Sodium Chloride Aldrich >99% Xyloglucan DSP Gokyo Food 100% and Chem. Co. Formic Acid Aldrich >96% Sodium Carbonate Aldrich >99%

Synthesis:

Melamine Formaldehyde Pre-Polymer Synthesis

[0103] 1) To a 250 ml reaction flask was added 19.5 g formalin (37 wt % aqueous formaldehyde) and 44 g water. [0104] 2) The pH of the solution was adjusted to 8.9 using 5 wt % sodium carbonate aqueous solution. [0105] 3) 10 g melamine and 0.6 g sodium chloride were added and the mixture stirred at 200 rpm using an overhead stirrer. [0106] 4) The mixture was heated to 62 C. and stirring continued until the mixture became clear (typically 1 hour). This solution contains 23.2 wt % trimethylol melamine and is hereinafter referred to as pre-polymer (1).

Xyloglucan Grafted Melamine Formaldehyde Microcapsule Synthesis

[0107] A number of xyloglucan grafted microcapsules were prepared containing 2, 1 or 0.5% xyloglucan (on particle weight). The weights used are given Table 7.

TABLE-US-00007 TABLE 7 Material: 2% XG 1% XG 0.5% XG Pre-Polymer (1) 13.4 13.4 13.4 Benzyl Acetate 26.9 26.9 26.9 Hostasol Yellow 3G 0.0054 0.0054 0.0054 Water 99.7 129.7 144.7 1% Xyloglucan Solution 60.0 30.0 15.0

[0108] The xyloglucan solution was prepared by dissolving 2 g of xyloglucan in 198 g of boiled water, using a homogeniser at 8,000 rpm for 5 minutes and allowing to cool prior to using. [0109] 1) The water was added to a 250 ml reaction flask and heated to 75 C. [0110] 2) The pre-polymer (1) was then added, and the pH was adjusted to 4.1 using 10 wt % formic acid. [0111] 3) After approximately 1 minute the solution became turbid. [0112] 4) A homogeniser (at 8,000 rpm) was then used to agitate the mixture while slowly adding the benzyl acetate over 30 seconds. [0113] 5) The mixture was agitated at this shear regime for a further 2 minutes. [0114] 6) The reaction vessel was then sealed and heated with overhead stirring (300 rpm) at 75 C. [0115] 7) The xyloglucan solution was added after 15 minutes. [0116] 8) The reaction was allowed to continue for a total of 3 hours. [0117] 9) The mixture was cooled and adjusted to pH 7 using 5 wt % sodium carbonate

[0118] The final dispersions were 15% particle solids, consisting of approximately 10% MF shell and 90% Benzyl Acetate, with 2 to 0.5% XG (on particle solids) attached.

Example 4Comparison of Particle Size of Xyloglucan Grafted Polyurea and Melamine Formaldehyde Microcapsules

[0119] The particle size for both the polyurea (PU) and melamine formaldehyde (MF) synthesized microcapsules was measured (using a Malvern Mastersizer 2000). The results are given in Table 8.

TABLE-US-00008 TABLE 8 XG Level Particle Size d(0.5) microns (%) PU MF 2 15.6 139.1 1 14.9 20.7 0.5 14.9 17.3

[0120] The PU synthesis route generates smaller particles and allows the incorporation of higher XG levels without inducing aggregation and increasing particle size.

Example 5Comparison of Laundry Liquid Stability of Xyloglucan Grafted Polyurea and Melamine Formaldehyde Microcapsules

[0121] The stability of the PU and MF microcapsules as used in Example 4 were compared within an unstructured laundry liquid detergent with composition in Table 9 (1 wt % of microcapsules added).

TABLE-US-00009 TABLE 9 Component % w/w Monopropylene Glycol 11 Glycerol 5 Monoethanolamine 7 Triethanolamine 2.5 Citric Acid 3.9 Neodol 25-7 4.6 LAS Acid 8.8 Prifac 5908 3 Dequest 2010 1.5 SLES 3EO 6.8 EPEI (Sokalan HP 20) 3 Acusol OP301 0.1 Sodium Sulphite 0.25 Water to 100%

[0122] Attachment of a nonionic polysaccharide to a microcapsule might be expected to slightly stabilize a dispersion of the particles. Surprisingly the same deposition polymer when added to polyurea microcapsules gave a visibly much more stable suspension of the particles after 3 days, whereas the corresponding melamine formaldehyde capsules with the same level of the same deposition polymer attached visibly settled out of the detergent liquid much more over the same time period.

Example 6Synthesis of Full Perfume Polyurea Microcapsule with Grafted Hydroxypropyl Cellulose

[0123] This example details the production of hydroxypropyl cellulose (HPC) grafted polyurea encapsulates containing a model perfume (rather than benzyl acetate only) and low levels of hydroxypropyl cellulose (0.3% on encapsulate weight). The materials used are similar to those in Example 1, with the exceptions that AKK perfume replaces benzyl acetate, 5% polyvinyl alcohol aqueous solution replaces 0.5% LAS solution and 1% hydroxypropyl cellulose aqueous solution replaces 1% XG solution. New material details are given in Table 1 and composition details are given in Table 2.

TABLE-US-00010 TABLE 10 Material Supplier % Active AKK Perfume Aldrich (for ingredients) - See 100% Table 11 for composition Polyvinyl Alcohol Aldrich 100% (Mowiol 18-88) Hydroxypropyl Cellulose Aldrich 100% (MW = 370K)

TABLE-US-00011 TABLE 11 (AKK Perfume Composition) Wt % Ingredient CAS 6.66 Manzanate 39255-32-8 6.66 Aldehyde C8 124-13-0 6.66 Tetra hydro linalol 78-69-3 6.66 Benzyl acetate 140-11-4 6.66 Linalyl acetate 115-95-7 11.7 OTBCA 88-41-5 1.66 Damascone, delta 57378-68-4 6.66 Aldehyde c12 112-54-9 6.66 Verdyl acetate 5413-60-5 6.66 Ionone beta 14901-07-6 6.66 Bangalol 28219-61-6 6.66 Iso E super (OTNE) 54464-57-2 6.66 Hexyl cinnamic aldehyde 101-86-0 6.66 Cyclopentadecanolide 106-02-5 6.66 Phenyl ethyl 2-phenylacetate 102-20-5

[0124] The weights and procedure were identical to that given in Example 1. The HPC solution was added 15 minutes after the reaction started.

[0125] The final dispersion was 10% particle solids, consisting of approximately 10% PU shell and 90% AKK Perfume, with 0.3% HPC (on particle solids) attached.

Example 7Synthesis of Comparative Full Perfume Melamine Formaldehyde Encapsulate with Grafted Hydroxypropyl Cellulose

[0126] A comparative example prepared at equivalent composition levels and an HPC addition time point of 15 minutes into microcapsule formation was prepared. This comparative example utilises MF shell rather than polyurea. The materials used were similar to those detailed in Example 3, with the exceptions that AKK perfume replaces benzyl acetate and 1% hydroxypropyl cellulose aqueous solution replaces 1% XG solution. New material details are given in Tables 10 and 11.

[0127] The weights and procedure were identical to that detailed in Example 3.

[0128] The final dispersion was 10% particle solids, consisting of approximately 10% MF shell and 90% AKK Perfume, with 0.3% HPC (on particle solids) attached.

Example 8Comparison of Laundry Liquid Stability of HPC Grafted Polyurea and Melamine Formaldehyde Microcapsules

[0129] The stability of the PU and MF microcapsules as described in Examples 6 and 7 were compared within an unstructured laundry liquid detergent. The inclusion levels and procedure were identical to that detailed in Example 5.

[0130] A clear difference in stability was observed after three days:

[0131] The MF encapsulate had completely phase separated and creamed to the top of the solution, whereas with the polyurea variant the stability is maintained.

Examples 9 to 15: Compositions

[0132] These examples show the use of the PU microcapsules in typical laundry, hair and skin body wash compositions. The materials used are given in Table 12.

TABLE-US-00012 TABLE 12 Component Specification LAS Linear Alkyl Benzene Sulphonic Acid Marlon AS3, ex. Huls Na-PAS Primary Alkyl Benzene Sulphonic Acid, neutralises with NaOH Dobanol 25-7 C12-15 Ethoxylated Alcohol, 7EO, ex Shell Zeolite Wassalith P, ex Degussa STPP Sodium Tri Polyphosphate, Thermphos NW, ex Hoechst Dequest 2066 Metal Chelating Agent, ex. Monsanto Lipolase Type 100L, ex. Novo Savinase 16L Protease, ex Novo Sokalan CP5 Acrylic/Maleic Builder Polymer, ex BASF Deflocculating Polymer Polymer A-11 disclosed in EP-A-346 995 SCMC Sodium Carboxymethyl Cellulose Texapon N 701 Sodium Laureth Sulphate, ex Cognis Aculyn 28 Polymer (20%) Carbomer, ex Rohm and Haas Tegobetaine CK Cocoamidopropyl Betaine, ex Goldschmidt BF Jaguar C14 Guar Hydroxypropyltrimonium Chloride, ex Aqualon DC 1788 Dimethiconol (and) TEA-Dodecylbenzene- sulfonate, ex Dow Corning Euperlan KE 4515 Glycol Distearate and Sodium Laureth Sulphate, Cocamidopropyl Betaine, ex Cognis BTAC Genamin BTLF, Behentrimonium Chloride, ex Aako Cetearyl Alcohol Lanette S3, ex. BASF DC5 7134 Silicone Emulsion, ex Dow Corning Carbopol Aqua SF-1 Acrylate Copolymer, Lubrizol SLES 1EO Sodium Lauryl Ether Sulphate (1EO), ex. BASF Cocamide MEA Cocamide monoethanolamine, ex Stepan Versene XL100 Ethylenediaminetetraacetic Acid Tetrasodium Salt, ex Dow Chemical PPG-9 Polypropylene Glycol, MW = 425 g, Dow Chemical Laundry Minors Anti-redeposition polymers, transition-metal scavengers, bleach stabilisers, fluorescers, antifoam, dye transfer inhibition polymers, enzymes, perfume

Example 9Spray-Dried Powder

[0133] Table 13 gives the composition of a spray dried laundry detergent powder containing PU microcapsules from Example 1.

TABLE-US-00013 TABLE 13 Component % w/w PU Microcapsules (from Example 1) 1.0 Na PAS 11.5 Dobanol 25-7 6.3 Soap 2.0 Zeolite 24.1 SCMC 0.6 Na Citrate 10.6 Na Carbonate 23.0 Sodium Polyacrylate (MW 1,300,000) 0.7 Dequest 2066 0.4 Sokalan CP5 0.9 Savinase 16L 0.7 Lipolase 0.1 Perfume 0.4 Water/salts Up to 100%

Example 10Laundry Detergent Granulate Prepared by Non-Spray Drying Method

[0134] Table 14 gives a granular laundry detergent composition containing the PU microcapsules of Example 1, as can be manufactured by a non-tower route.

TABLE-US-00014 TABLE 14 Component % w/w PU Microcapsules (from Example 1) 1.0 Na PAS 13.5 Dobanol 25-7 2.5 STPP 45.3 Na Carbonate 4.0 Polyacrylamide (MW 5,500,000) 2.8 Na Silicate 10.1 Perfume 1.0 Minors 1.5 Water Up to 100%

Example 11Isotropic Laundry Liquid

[0135] Table 15 gives an isotropic laundry liquid composition incorporating the PU microcapsules of Example 1.

TABLE-US-00015 TABLE 15 Component % w/w PU Microcapsules (from Example 1) 1.0 Na Citrate 10.7 Propylene Glycol 7.5 Ethylene Glycol 4.5 Borax 3 Savinase 16L 0.3 Lipolase 0.1 Dextran (MW 800,000) 1.0 Monoethanolamine 0.5 Cocofatty Acid 1.7 NaOH (50%) 2.2 LAS 10.3 Dobanol 25-7 6.3 LES 7.6 Perfume 1.0 Minors (adjust pH to 7 with NaOH) 1.3 Water Up to 100%

Example 12Structured Laundry Liquid

[0136] Table 16 gives a structured liquid laundry detergent composition incorporating the PU microcapsules of Example 1.

TABLE-US-00016 TABLE 16 Component % w/w PU Microcapsules (from Example 1) 1.0 LAS 16.5 Dobanol 25-7 9.0 Oleic Acid (Priolene 6907) 4.5 Zeolite 15.0 KOH (neutralising acids to pH 7) 8.5 Citric Acid 8.2 Deflocculating Polymer 1.0 Protease 0.38 Lipolase 0.2 Imacol C (ex Clariant) 2.0 Perfume 1.0 Minors 0.4 Water Up to 100%

Example 13Hair Shampoo

[0137] Table 17 gives a hair shampoo composition incorporating the PU microcapsules of Example 1.

TABLE-US-00017 TABLE 17 Composition % w/w PU Microcapsules (from Example 1) 1.0 Texapon N701 12.8 Aculyn 28 Polymer (20%) 1.0 Tegobetaine CK 1.6 BF Jaguar C14 0.15 DC 1788 3.0 Emperlan KE 4515 2.5 Propylene Glycol 0.25 Sodium Hydroxide 0.2 Perfume 2.0 Water Up to 100%

Example 14Hair Conditioner

[0138] Table 16 gives a hair conditioner composition incorporating the PU microcapsules of Example 1.

TABLE-US-00018 TABLE 16 Composition % w/w PU Microcapsules (from Example 1) 1.0 BTAC 2.9 Cetearyl Alcohol 4.0 DC5 7134 2.5 Perfume 1.0 EDTA 0.1 Potassium Chloride 0.1 Water Up to 100%

Example 15Skin Body Wash

[0139] Table 17 gives a skin body wash composition incorporating the PU microcapsules of Example 1.

TABLE-US-00019 TABLE 17 Composition % w/w PU Microcapsules (from Example 1) 1.0 Carbopol Aqua SF-1 1.2 SLES 1EO 11.0 Cocamide MEA 1.0 EDTA 0.05 PPG-9 0.1 NaCl (25% solution) 1.0 Perfume 1.0 NaOH (50% solution) 0.01 Water Up to 100%

[0140] Examples 9 to 15 may alternatively be formulated using the HPC grafted microcapsule from Example 6.