Title of Invention	AN IMPROVED DOMESTIC METHOD OF TREATING A TEXTILE GARMENT
Abstract	The present invention provides a treatment composition comprising a hydrophobic dye.

Full Text

C4441/C FORM - 2 THE PATENTS ACT, 1970 (39 of 1970) & The Patents Rules, 2003 COMPLETE SPECIFICATION (See Section 10 and Rule 13) LAUNDRY TREATMENT COMPOSITIONS HINDUSTAN LEVER LIMITED, a company incorporated under the Indian Companies Act, 1913 and having its registered office at Hindustan Lever House, 165/166, Backbay Reclamation, Mumbai-400 020, Maharashtra, India The following specification particularly describes the invention and the manner in which it is to be performed PCT/EP2005/009846 1 – LAUNDRY TREATMENT COMPOSITIONS TECHNICAL FIELD The present invention relates to laundry treatment 5 compositions that comprise a dye. BACKGROUND OF THE INVENTION Garments comprising polyester fibres are ubiquitous. Many garments are white but over the lifetime of these garments 10 the whiteness is dulled reducing the aesthetic value of the garment. There is a need to maintain the white appearance of such garments such that the aesthetic value is retained as long as possible. 15 Bleach, fluorescers and shading agents are used in modern wash processes to maintain whiteness. The fluorescers and shading; agents that are currently available, do not deposit on polyester fibres of garments to a significant degree. All fibres may be subjected to a bleaching process but over time 20 such treatment can lead to the garment taking a yellow hue. There is a need to provide technology that maintains and enhances the white appearance of polyester comprising garments. 25 SUMMARY OF THE INVENTION Dyes disclosed herein are known to be used to dye textiles in industrial processes conducted at high temperatures together with high concentrations of dyes and dispersion 30 agents. Surprisingly the dyes can be used to shade at low levels of dye and surfactant and at routine laundry WO 2006/045375 PCT7EP2005/009846 - 2 - temperatures. We have found that hydrophobic dyes are substantive to polyester fibres under normal domestic wash conditions. At low levels of dye a shading whiteness benefit is provided. 5 In one aspect the present invention provides a laundry treatment composition comprising between 0.0001 to 0.1 wt % of a hydrophobic dye selected from benzodifuranes, methine, triphenylmethanes, napthalimides, pyrazole, napthoquinone 10 and mono-azo or di-azo dyes, and between 2 to 60 wt % of a surfactant. It is preferred that the dye is a mono-azo dye. In another aspect the present invention provides a method of treating a textile, the method comprising the steps of: 15 (i) treating a textile with an aqueous solution of the hydrophobic dye, the aqueous solution comprising from 1 ppb to 6 ppm of the hydrophobic dye and from 0.2 g/L to 3 g/L of a surfactant; and, {ii) rinsing and drying the textile. It is preferred that the aqueous solution has an ionic strength 20 from 0.001 to 0.5. It is preferred that the hydrophobic dye is present in the range 10 ppb to 200 ppb. In another aspect it is preferred that the aqueous solution also comprises from'1-ppb to 5 ppm one or more other dyes selected from cotton substantive shading dyes of group consisting of: 25 hydrolysed reactive dye; acid dye; and direct dye. A "unit dose" as used herein is a particular amount of the laundry treatment composition used for a type of wash, conditioning or requisite treatment step. The unit dose may 30 be in the form of a defined volume of powder, granules or tablet or unit dose detergent liquid. WO 2006/045375 PCT/EP2005/009846 - 3 - DETAILED DESCRIPTION OF THE INVENTION .Typical dye suppliers may be found,in the colour index, and include Clarianf, Dystar, Ciba & BASF. 5 Hydrophobic dyes are defined as organic compounds with a maximum extinction coefficient greater than 1000 L/mol/cm in the wavelength range of 400- to 750 nm and that are uncharged in aqueous solution at a pH in the range from 7 to 11. The hydrophobic dyes are devoid of polar solubilizing groups. In 10 particular the hydrophobic dye does not contain any sulphonic acid, carboxylic acid, or quaternary ammonium groups. The dye chromophore is preferably selected from the group comprising: azo; methine,' pyrazole napthoquinone, phthalocyanine; and, triphenylmethane chrpmophores. Most 15 preferred are azo dye chromophores. Many examples of hydrophobic dyes are found in the classes of solvent and disperse dyes. 20 Shading of white garments may be done with any colour "depending on consumer preference. Blue and Violet are particularly preferred shades and consequently preferred dyes or mixtures of dyes are ones that give a blue or violet shade on white polyester. 25 It is preferred that the dye(s) have a peak absorption wavelength of from 550nm to 650nm, preferably from 570nm to 630nm. A combination of dyes may be used which together have the visual effect on the human eye as a single dye having a 30 peak absorption wavelength on polyester of from 550nm to 650nm, preferably from 570nm to 630nm. This may be provide WO 2006/045375 PCT/EP2005/009846 - 4 - for example by mixing a red and green-blue dye to yield a blue or violet shade. A wide.range of suitable solvent and disperse dyes are 5 available. However detailed toxicological studies have shown that a number of such dyes are possible carcinogens, such dyes are not prererred. Preferred mono-azo dyes are of the torm: 10 wherein R3 and R4 are optionally substituted C2 to C12 alkyl chains having optionally therein ether (-0-) or ester links, 15 the chain being optionally substituted with -CI, -Br, -CN, -N02, and -SO2CH3; and, D denotes an aromatic or hetroaromatic group. Preferably D is selected from the group consisting of: azothiophenes, azobenzothiazoles and azopyridones. 20 It is preferred that R3 is -CH2CH2R5 and R4 and is -CH2CHZRb and R5 and R6 are independently selected from the group consisting of: H, -CN, -OH, -C6H5, -OCOR7 and -COOR7, and that R7 is independently selected from: aryl and alkyl. Preferred aryl are -C6H5 and C10H7. 25 The following is an example of a preferred class of mono-azo dyes: WO 2006/045375 PCT/EP2005/009846 - 5 - 10 15 20 25 where X and Y are independently selected from the group consisting of:- -H, -CI,. -Br, -CN, -N02, and -S02CH3; A is selected -H, -CH3, -CI, and -NHCOR; B is selected -H, -OCH3, -OC2H5, and -CI; R1 and R2 are independently, selected from the group consisting of: -H, -CN, -OH, -OCOR, -COOR, -aryl; and R is Cl-C8-alkyl. The following are preferred azo dyes: Disperse blue 10, 11, 12, 21, 30, 33, 36, 38, 42, 43, 44, 47,79, 79:1, 79:2, 79:3, 82, 85, 88, 90, 94, 96, 100, 101, 102, 106, 106:1, 121, 122, 124, .125, 128, 130, 133, 137, 138, 139, 142, 146, 148, 149, 165, 165:1, 165:2, 165:3, 171, 173, 174, 175, 177, 183, 187, 189, 193, 194, 200, 201, 202, 205-, 206, 207, 209, 210, 211,. 212, 219, 220, 222, 224, 225, 248, 252, 253,, 254, 255, 256, 257, 258, 259, 260, 264, 265, 266, 267, 268, 269,.270, 278, 279, 281, 283, 284, 285, 286, 287, 290, 291, 294, 295, 301, 303,-304, 305, 313, 315, 316, 317, 319, 321, 322, 324, 328, 330, 333, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 351, 352, 353, 355, 356, 358, 360, 366, 367, 368, 369, 371, 373, 374, 375, 376 and 378, Disperse Violet 2, 3, . 5, 6, 7, 9, 10, 12, 13, 16, 24, 25, 33, 39, 42, 43, 45, 48, 49, 50, 53, 54, 55, 58, 60, 63, 66, 69, 75, 76, 77, 82, 86, 88, 91, 92, 93, 93:1, 94, 95, 96, 97, 98, 99, 100, 102, 103, 104, 106 or 107, Dianix violet cc, and dyes with CAS-No!s WO 2006/045375 PCT/EP2005/009846 - 6 - 42783-06-2,'210758-04-6, 104366-25-8, 122063-39-2, 167940-11-6, 52239-04-0, 105076-77-5, 84425-43-4, and 87606-56-2. The following are preferred non-azo dyes: Disperse Blue 250, 5 354, 364, 366, Solvent Violet 8, solvent blue 43,solvent blue 57, Lumogen F Blau 650, and Lumogen F Violet 570. It is preferred that the dye is fluorescent. 10 The composition may also comprise between 0.0001 to 0.1 wt.'% of one or more other dyes selected from cotton substantive shading dyes of group consisting of: hydrolysed reactive dye; acid dye; and direct dye. 15 BALANCE CARRIERS AND ADJUNCT INGREDIENTS The laundry treatment composition in addition to the dye comprises the balance carriers and adjunct ingredients to 100 wt % of the composition. 20 These may be, for example, surfactants, builders, foam agents, anti-foam agents, solvents, fluorescers, bleaching agents, and enzymes. The use and amounts of these components are such that the composition performs depending upon economics, environmental factors and use of the composition. 25 The composition may comprise a surfactant and optionally other conventional detergent ingredients The composition may also comprise an enzymatic detergent composition which comprises from 0.1 to 50 wt %, based on the total detergent 30 composition, of one or more surfactants. This surfactant system may in turn comprise 0 to 95 wt % of one or more WO 2006/045375 PCTVEP2005/009846 - 7 - anionic surfactants and 5 to 100 wt % of one or more nonionic surfactants. The surfactant system may-additionally contain amphoteric or zwitterionic detergent compounds, but this in not normally desired owing to their relatively high 5 cost. The enzymatic detergent composition according to the invention will generally be used as a dilution in water of about 0.05 to 2 wt%. It is preferred that the composition comprises between 2 to 10 60 wt % of a surfactant, most preferably 10 to 30 wt %. Ir general, the nonionic and anionic surfactants of the surfactant system may be chosen from the surfactants described "Surface Active Agents" Vol. 1, by Schwartz & Perry,- Interscience 1949, Vol. 2 by Schwartz, Perry & Berch, 15 Interscience 1958," in the current edition of "McCutcheon' s " Emulsifiers and Detergents" published by Manufacturing Confectioners Company or in "Tenside-Taschenbuch", H. Stache, 2nd Edn., Carl Kauser Verlag, 1981. 20 Suitable nonionic detergent compounds which may be used include, in particular, the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone 25 or with propylene oxide. Specific nonionic detergent compounds are Cg to C22 alkyl phenol-ethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic Cs to Ci8 primary or secondary linear or 30 branched alcohols with .ethylene oxide, generally 5 to 40 EO. WO 2006/045375 PCT/EP2005/009846 - 8 - Suitable anionic detergent compounds which may be used are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about '8-to about 22 carbon atoms, the term alkyl being 5 used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic detergent compounds are sodium, and potassium alkyl sulphates, especially those obtained by sulphating higher C8 to Ci8 alcohols, produced for example from tallow or coconut oil, sodium and potassium 10 alkyl Cg to C20 benzene sulphonates, particularly sodium linear secondary alkyl C10 to C15 benzene sulphonates; and sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil .and synthetic alcohols derived from petroleum. The 15 preferred anionic detergent compounds are sodium C11 to C15 alkyl benzene sulphonates and sodium C12 to C18 alkyl sulphates. Also applicable are surfactants such as those described in EP-A-328 177 (Unilever), which show resistance to salting-out, the alkyl polyglycoside surfactants 20 described in EP-A-070 074, and alkyl monoglycosides. Preferred surfactant systems are mixtures of anionic with nonionic detergent active materials, in particular the groups and examples of anionic and nonionic surfactants 25 pointed out in EP-A-346' 995 (Unilever). Especially preferred is surfactant system that is a mixture of an alkali metal salt of a C16 to C18 primary alcohol sulphate together with a C12 to C15 primary alcohol 3 to 7 EO ethoxylate. 30 The nonionic detergent is preferably present in amounts greater than 10%, e.g. 25 to 90 wt % of the surfactant WO 2006/045375 PCT/EP2005/009846 - 9 - system. Anionic surfactants can be present for example in amounts in the-range from about 5% to about 40 wt % of the surfactant system. 5 CATIONIC COMPOUND When the present invention is used as a fabric conditioner it needs to contain a cationic compound. Most preferred are quaternary ammonium compounds. 10 It is advantageous if the quaternary ammonium compound is a quaternary ammonium compound having at least one C12 to c\«2 alkyl chain. 15 It is preferred if the quaternary ammonium compound has the following formula: in which Rl is a C12 to C22 alkyl or alkenyl chain; R2, R3 and R4 are independently selected from C1 to C4 alkyl chains and 20 X" is a compatible anion. A preferred compound of this type is the quaternary ammonium compound cetyl trimethyl quaternary ammonium bromide. A second class of materials for use with the present 25 invention are the quaternary ammonium of the above structure in which R1 and R2 are independently selected from C12 to C22 alkyl or alkenyl chain; R3 and R4 are independently selected from C1 to C4 alkyl chains and X~ is a compatible anion. WO 2006/045375 PCT/EP2005/009846 - 10 - A detergent composition according to claim 1 in which the ratio of.(ii) cationic material to (iv) anionic surfactant is at least 2:1. 5 Other suitable .quaternary ammonium compounds are disclosed in EP 0 239 '910 (Procter, and Gamble). It is preferred if the ratio of cationic to nonionic surfactant is from 1:100 to 50:50, more preferably 1:50 to 10 20:50. The cationic compound may be present from 0.02 wt % to 20 wt % of the total weight of the composition. 15 Preferably the cationic compound may be present....from 0.05 wt % to 15 wt %, a more preferred composition range is from 0.2 wt % to 5 wt %, and most preferably the composition range is from 0.4 wt % to 2.5 wt % of the total weight of the composition. 20 If the product is a liquid it is preferred if the level of cationic surfactant is from 0.05 wt % to 10 wt % of the total weight ,of the composition. Preferably the cationic compound may be present from 0.2 wt % to 5 wt %, and most 25 preferably from 0.4 wt % to 2.5 wt % of the total weight of the composition. If the product is a solid it is preferred if the level of cationic surfactant is 0.05 wt % to 15 wt % of the total 30 weight of the composition. A more preferred composition range is from 0.2 wt % to 10 wt %, and the most preferred WO 2006/045375 PCT/EP2005/009846 - 11 - composition range is from 0.9 wt % to 3.0 wt % of the total weight of the composition. BLEACHING SPECIES 5 The laundry treatment composition may comprise bleaching species. The bleaching species, for example, may selected from perborate and percarbonate; These peroxyl species may be further enhanced by the use of an activator, for example, TAED or SNOBS. " Alternatively or in addition to, a 10 transition metal catalyst may used with the peroxyl species. A transition metal catalyst may also be used in the absence of peroxyl species where the bleaching is termed to be via atmospheric oxygen, see, for example WO02/4 8 301. Photobleaches, including singlet oxygen photobleaches, may 15 be used with the laundry treatment composition. A preferred photobleach is vitamin K3. FLUORESCENT AGENT The laundry treatment composition most preferably comprise? 20 .a fluorescent agent(optical brightener). Fluorescent agent: are well known and many such fluorescent agents am available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts. The total amount of 25 the fluorescent agent or agents used in laundry treatment composition is generally from 0.005 to 2 wt %, more preferably 0.01 to 0.1 wt %. Preferred classes of fluorescer are: Di-styryl biphenyl compounds, e.g. Tinopal (Trade Mark) CBS-X, Di~amine stilbene di-sulphonic acid compounds, e.g. 30 Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH, and Pyrazoline compounds, e.g. Blankophor SN. Preferred WO 2006/045375 PCTYEP2005/009846 - 12 - fluorescers are: sodium 2 (4~styryl-3-sulfophenyl)-2H-napthol[l,2-d]trazple, disodium 4, 4 -bis{ [ (4-anilino~6- {N methyl-N-2 hydroxyethyl) amino 1,3,5-triazin-2-yl)]amino}stilbene-2-2' disulfonate, disodium 4,4'-bis{[(4- 5 anilino-6-morpholino-l, 3,5-triazin-2-yl)3 amino} stilbene-2-2' disulfonate, and disodium 4,4'-bis{2-sulfoslyryl)biphenyl. EXAMPLES 10 Example 1 Approximately 1000 ppm solutions of the dyes listed in the table below, were made in ethanol. 15 A stock solution of 1.8g/L of a base washing powder in water was. created. The washing powder contained 18% NaLAS, 73% salts (silicate, sodium tri-poly-phosphate, sulphate, carbonate), 3% minors including perborate, fluorescer and enzymes, remainder impurities and water. The solution was 20 divided into 100ml aliquots and the solvent dyes added from the ethanol solutions to give 5.8 ppm solutions. 1 g of pure woven polyester fabric was added to each of the wash solutions and the solution then shaken for 30 minutes, rinsed and dried. From the colour of the fabric it was clear 25 that dye had deposited to the fabric. To quantify this the colour was measured using a reflectance spectrometer and expresses as the deltaE value compared to a polyester washed analogously but without dye present. WO 2006/045375 PCT7EP2005/009846 - 13 - The results are given below WO 2006/045375 PCT/EP2005/009846 - 14 - Example 2 50 ppm solutions of the dyes listed in the table below, were made in ethanol. Concentration refers to. dyes as received- 5 from the supplier. In general solvent dyes are pure (>90%) and,disperse dyes have purities in the range 20-50%. A stock solution of 1.8g/L of a base washing powder in water was created. The washing powder contained 18% NaLAS, 73% 10 salts (silicate, sodium tri-poly-phosphate, sulphate, .carbonate), 3% minors including perborate, fluorescer and enzymes, remainder impurities and water. The solution was divided into 100ml aliquots and the dyes added from the ethanol solutions with rapid stirring.to give 200ppb 15 solutions. 1 g of pure knitted polyester fabric was added to each of the wash solutions and the solution then shaken for 30 minutes, rinsed and dried. From the colour of, the fabric it was clear that dye had deposited to the fabric. To quantify this the colour was measured using a reflectance 20 spectrometer and expresses as the delta E value compared to a polyester washed analogously but without dye present. Following the washes the Ganz whiteness of the cloth was also measured (see "assessment of Whiteness and Tint of Fluorescent Substrates with Good Instrument Correlation" 25 Colour Research and Application 19, 1994).. The experiments were repeated using knitted nylon as a fabric type. WO 2006/045375 PCT/EP2005/009846 - 15 – The results are displayed in the table below. WO 2006/045375 PCT/EP2005/009846 - 16 - Table - notes The ganz whiteness values are accurate to +/-5 units. All deltaE measurements are UV excluded. 5 Only where known is the structure of the dye given. The optical density, OD, is that of a 200ppb solution in water at 10cm. The value was obtained by extrapolated from WO 2006/045375 PCT/EP2005/009846 - 17 - from measurement in ethanol solutions at higher levels for accuracy. CT is a measure of the Colour Transferred from the wash 5 solution to the polyester and is defined as: CT - deltaE/OD From the deltaE results in the table all the dyes coloured 0 the polyester. From the Ganz results, dyes which are blue or violet increase the whiteness. The Black and red dyes decrease the whiteness. The lumogen dyes add fluorescence to the polyester, as 5 observed by eye in a light box with UV-irradiation. Example 3 The experiment of example 2 was repeated, but using 40 ppb of the dyes listed below. The L:C was changed to 30:1 and 0 consisted by weight of 43% woven polyester and 57% non-mercerised cotton sheeting. The Ganz whiteness of the polyester was 89 for disperse blue 79:1. Whiteness benefits were also observed on the cotton. Repetition of the experiment using nylon, also gave benefits. (C) COM-NAT Phase Entry Amendment 18 We claim: 1. A domestic method of treating a textile garment, the method comprising the steps of: (i) treating a textile with an aqueous solution of a blue or violet hydrophobic dye, the aqueous solution comprising from 1 ppb to 5 ppm of the hydrophobic dye and from 0.2 g/L to 3 g/L of a surfactant; and, (ii) rinsing and drying the textile, wherein the hydrophobic dye is selected from: benzodifuranes; methine; triphenylmethanes; napthalimides; pyrazole ,-napthoquinone; mono-azo and di-azo dyes. 2. A domestic method of treating a textile according to claim 1, wherein the hydrophobic dye is a disperse or solvent dye. 3. A domestic method of treating a textile according to claim 1 or 2, wherein the dye is a mono-azo dye. 4. A domestic method of treating a textile according to claim 3, wherein the mono-azo dye is selected from a compound of the following formula: D-N=N wherein R3 and R4 are optionally substituted C2 to C12 alkyl chains having optionally therein ether (-0-) or ester links, the chain being optionally substituted with COM-NAT Phase Entry Amendment - 19 - -CI, -Br, -CN, -N02, and -S02CH3; and, D denotes an aromatic or hetroaromatic group. 5. A domestic method of treating a textile according to claim 4, wherein R3 is -CH2CH2R5 and R4 and is -CH2CH2R6 and R5 and R6 are independently selected from the group consisting of: H, -CN, -OH, -C6H5, -0C0R7 and -C00R7, wherein R7 is independently selected from: aryl and alkyl. 6. A domestic method of treating a textile according to claim 5, wherein the aryl is -C6H5 or C10H7. 7. A domestic method of treating a textile according to anyone of claims 4 to 6, wherein D is selected from the group consisting of: azothiophenes, azobenzothiazoles and azopyridones. 8. A domestic method of treating a textile to claim 3, wherein the mono-azo is of the form: where X and Y are independently selected from the group consisting of: -H, -Cl, -Br, -CN, -N02, and -S02CH3. A is selected -H, -CH3, -Cl, and -NHCOR; B is selected -H, -OCH3/ -OC2H5, and -Cl; (C) COM-NAT Phase Entry Amendment - 20 - R1 and R2 are independently selected from the group consisting of: -H, -CN, -OH, -0C0R, -COOR, -aryl; and, R is Cl-C8-alkyl. 9. A domestic method of treating a textile according to claim 1, wherein the dye is selected from the group consisting of: Disperse blue 10, 11, 12, 21, 30, 33, 36, 38, 42, 43, 44, 47,79, 79:1, 79:2, 79:3, 82, 85, 88, 90, 94, 96, 100, 101, 102, 106, 106:1, 121, 122, 124, 12 5, 12 8, 130, 133, 13 7, 13 8, 139, 142, 146, 148, 149, 165, 165:1, 165:2, 165:3, 171, 173, 174, 175, 177, 183, 187, 189, 193, 194, 200, 201, 202, 205, 206, 207, 209, 210, 211, 212, 219, 220, 222, 224, 225, 248, 252, 253, 254, 255, 256, 257, 258, 259, 260, 264, 265, 266, 267, 268, 269, 270, 278, 279, 281, 283, 284, 285, 286, 287, 290, 291, 294, 295, 301, 303, 304, 305, 313, 315, 316, 317, 319, 321, 322, 324, 328, 330, 333, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 351, 352, 353, 355, 356, 358, 360, 366, 367, 368, 369, 371, 373, 374, 375, 376 and 378, Disperse Violet 2, 3, 5, 6, 7, 9, 10, 12, 13, 16, 24, 25, 33, 39, 42, 43, 45, 48, 49, 50, 53, 54, 55, 58, 60, 63, 66, 69, 75, 76, 77, 82, 86, 88, 91, 92, 93, 93:1, 94, 95, 96, 97, 98, 99, 100, 102, 103, 104, 106 or 107, Dianix violet cc, and dyes with CAS-No's 42783-06-2, 210758-04-6, 104366-25-8, 122063-39-2, 167940-11-6, 52239-04-0, 105076-77-5, 84425-43-4, and 87606-56-2. 10. A domestic method of treating a textile according to claim 1, wherein the dye is selected from the group consisting of: Disperse Blue 250, 354, 364, 366, Solvent (C) COM-NAT Phase Entry Amendment - 21 - Violet 8, solvent blue 43,solvent blue 57, Lumogen F Blau 650, and Lumogen F Violet 570. 11. A domestic method of treating a textile according any one of claims 1 to 3, wherein the dye is selected is fluorescent. 12. A domestic method of treating a textile according to any preceding claim, wherein the laundry treatment composition comprises a fluorescer other than the dye per se. 13. A domestic method of treating a textile according to any preceding claim, wherein the dye gives a blue or violet shade when deposited on white polyester. 14. A domestic method of treating a textile according to any preceding claim, wherein the hydrophobic dye is present in the range 10 ppb to 200 ppb. 15. A domestic method of treating a textile according to claim 13 or 15, wherein the aqueous solution has an ionic strength from 0.001 to 0.5. 16. A domestic method of treating a textile according to any preceding claim, wherein the aqueous solution comprises from 1 ppb to 6 ppm one or more other dyes selected from cotton substantive shading dyes of group consisting of: hydrolysed reactive dye; acid dye; and direct dye. Dated this 20th day of March 2007

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