AU2010291392A1

AU2010291392A1 - Composition and process for treatment of a fabric

Info

Publication number: AU2010291392A1
Application number: AU2010291392A
Authority: AU
Inventors: Sameer Keshav Barne; Aravindakshan Perincheery; Abhishek Rastogi; Archana Sinha
Original assignee: Unilever PLC
Current assignee: Unilever PLC
Priority date: 2009-09-02
Filing date: 2010-08-12
Publication date: 2012-02-23
Anticipated expiration: 2030-08-12
Also published as: CN102575197A; CA2770869A1; ZA201200792B; ES2531418T3; CN102575197B; AU2010291392B2; EA201200401A1; BR112012003018A2; EP2473590B2; EP2473590B1; EA022063B1; WO2011026718A1; AR078146A1; ES2531418T5; MX2012002748A; EP2473590A1; CL2012000538A1

Abstract

It is an object to provide a composition and process for treatment of a fabric that improves efficacy of subsequent cleaning. The present inventors have found that a composition comprising a carboxylic acid polymer that has been neutralised at least partially to the salt form and a second polymer, capable of forming hydrogen bonds with the first polymer in the present of an acid, provides both a secondary cleaning benefit and good storage stability, without forming polymer-polymer complex when it is in the solid formulation and give a complex when dispersed in water.

Description

WO 2011/026718 PCT/EP2010/061744 COMPOSITION AND PROCESS FOR TREATMENT OF A FABRIC Technical Field The present invention relates to a process for treatment of a fabric. It further relates to 5 a composition and a kit for treatment of a fabric. The invention will be described hereinafter with reference to this application. However, it will be appreciated that the invention is not limited to this particular field of use. Background and Prior Art 10 Any discussion of the prior art throughout the specification should in no way be considered as an admission that such prior art is widely known or forms part of the common general knowledge in the field. Better cleaning of fabric articles during washing has been the primary focus of laundry 15 detergent research for decades. However, since the present day consumer has ever higher demands for the effectiveness of washing detergents, substantial improvements remain to be desired. US2006046950A (Penninger and Bastigkeit, 2006) teaches a detergent composition 20 for cleaning textile materials comprising a combination of a soil release-capable alkyl or hydroxyalkyl cellulose derivative and a hygroscopic polymer selected from the class consisting of polypeptides, hydrogels, polyvinyl alcohol, the polyalkylene glycols, the homopolymers of acrylic acid, methacrylic acid, and maleic acid, copolymers of acrylic acid, methacrylic acid, and maleic acid and mixtures of the homo and copolymers. 25 The use of the hygroscopic polymers in combination with the cellulose derivatives is said to result in improved cleaning performance. EP0256696 (Unilever, 1988) teaches that improvement in soil suspension is achieved by adding mixture of vinyl pyrrolidone polymer and a nonionic cellulose ether to a 30 detergent composition. GB994353 (Domestos, 1965) teaches that mixtures of certain polymeric materials, when incorporated into unbuilt detergent compositions based on synthetic surface active agents, provide enhanced anti-redeposition as compared to WO 2011/026718 PCT/EP2010/061744 2 activity of individual polymers alone when added alone to same detergent compositions. US3771951 (Berni et al, 1973) and GB133803 (Gaf Corp, 1973) teach that detergent 5 composition comprising a water soluble detergent and a mixture of water soluble polyvinyl alcohol and a water soluble poly vinyl pyrollidone exhibits enhanced degree of soil suspension The above methods are reported to provide improved antiredeposition of soils and 10 better cleaning of fabrics. However, reduction in subsequent post-wash soiling of fabrics is not reported. Further, the cleaning compositions essentially comprise of a surfactant and the pH of wash liquor is alkaline or neutral. US4007305 (Kakar et al, 1977) addresses the problem of providing satisfactory 15 nondurable finishes to textiles which impart optimum soil release and soil repellent properties. According to D5, the textiles must be treated with an alkaline aqueous medium having pH value of 7.5-11 and containing water soluble hydrophilic soil release polymer having carboxylic acid groups and a dispersed hydrophobic soil repellent fluorochemical. 20 On the other hand, various industrial treatments for fabric modification are known to render the fabric less prone to soiling. The fabric modification of this type is normally carried out during textile manufacture. The treatments, besides being substrate specific, are relatively difficult to practice in household. 25 In view of the shortcomings of the prior art, one of the objects of the present invention is to provide a process for reducing soiling of fabrics that can be easily used in the household. Another object of the present invention is to provide a process of treatment of a fabric 30 for reducing soiling of fabrics. Yet another object of the present invention is to provide a process for treatment of a fabric that improves efficacy of subsequent cleaning.

WO 2011/026718 PCT/EP2010/061744 3 Yet another object of the present invention is to provide a process for reducing soiling of fabrics that allows enhanced deposition of benefit agents, such as perfume and fluorescer. 5 Yet another object of the present invention is to provide a process for treatment of a fabric which is effective on various types of fabrics such as cotton, polyester and polycotton. Yet another object of the present invention is to provide a process for treatment of a 10 fabric which is relatively easy to practice in household. It is yet another object of the present invention to provide such a composition either solid or liquid and process for easier cleaning in the form of a single product having good storage stability. 15 Surprisingly it is found that a mixture of two or more complex forming polymers, wherein one of the polymers is shielded from the other by using a stabilizer solves the problem of stability due to complex formation during storage, while providing the desired cleaning benefit. 20 The present inventors have found that a composition comprising a carboxylic acid polymer that has been neutralised at least partially to the salt form and a second polymer, capable of forming hydrogen bonds with the first polymer in the present of an acid, provides both a secondary cleaning benefit and good storage stability, without 25 forming polymer-polymer complex when it is in the solid formulation and give a complex when dispersed in water. The present inventors also have been found that a liquid composition of two polymers dispersed in a solvent in presence of a stabilizer provides a stable preformed complex 30 at high concentration with very good storage stability and it provides a secondary cleaning benefit.

WO 2011/026718 PCT/EP2010/061744 4 Summary of the invention According to a first aspect , the present invention provides a base composition comprising a mixture of polymer A and a stabilizer wherein the polymer A is selected 5 from the group of homopolymers and copolymers of carboxylic acid and derivatives;, a polymer B selected from the group of homopolymers and copolymers of alkylene oxides having a molecular mass greater than 2x104 D, vinyl pyrrolidone and/or their derivatives; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose and/or their derivates; and a pH adjustment agent 10 selected from organic acids, selected from citric acid, formic acid, oxalic acid, phtalic acid ascorbic acid, glutamic acid, salicylic acid, tartaric acid, pyroglutamic acid, malic acid, maleic acid, malonic acid, succinic acid, glutaric acid, adipic acid, propane 1,2,3 tricarboxylic acid, butane 1,2,3,4 tetra carboxylic acid and their anhydides, inorganic acids and/or buffers. 15 According to a second aspect, the present invention provides a wash or rinse liquor comprising between 0.02 and 40 g/l of the composition according to the invention, having a pH of< 6 20 According to a third aspect, the present invention provides a process for washing fabric comprising the steps in sequence of contacting the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/l of the composition according to the invention; leaving the fabric to dry; leaving the fabric for soil and/or dirt to deposit onto the fabric; washing the fabric with a conventional washing detergent in a conventional 25 way. According to a fourth aspect, the present invention provides a process for preparing the solid composition according to the invention comprising the steps of: mixing Polymer A with the inorganic alkalinity source; and mixing the mixture from the 30 previous step with the Polymer B and the pH adjustment agent.

WO 2011/026718 PCT/EP2010/061744 5 According to a fifth aspect, the present invention provides a process for preparing the liquid composition according to the invention comprising the steps of: (a) preparing solution of polymer A and polymer B separately with or without the stabilizer (b) adding the stabilizer if it is not added while preparing the solution of polymer A and 5 polymer B and then (c) Mixing the both solution and stirring it with the pH adjustment agent. By mentioning the term storage stability here we mean, that such a formulation in powder form exhibit no complex formation between the interacting polymers and it 10 readily forms the complex when dispersed in water and in liquid form the complex will be well dispersed and not precipitated in the composition. By secondary cleaning benefit is meant that a fabric treated with the composition exhibits benefits such as reduction in soiling, ease of subsequent cleaning and/or enhanced deposition of benefit agents. 15 These and other aspects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. For the avoidance of doubt, any feature of one aspect of the present invention may be utilised in any other aspect of the invention. The word 20 "comprising" is intended to mean "including" but not necessarily "consisting of" or "composed of." In other words, the listed steps or options need not be exhaustive. It is noted that the examples given in the description below are intended to clarify the invention and are not intended to limit the invention to those examples per se. Similarly, all percentages are weight/weight percentages unless otherwise indicated. 25 Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description indicating amounts of material or conditions of reaction, physical properties of materials and/or use are to be understood as modified by the word "about". Numerical ranges expressed in the format "from x to y" are understood to include x and y. When for a specific feature multiple preferred 30 ranges are described in the format "from x to y", it is understood that all ranges combining the different endpoints are also contemplated.

WO 2011/026718 PCT/EP2010/061744 6 Detailed description of the invention The present invention thus aims for a composition in form of a solid or liquid and process for the application of a sacrificial layer of polymeric material onto a fabric surface, before dirt and/or soil is deposited onto the fabric. Upon the subsequent 5 (conventional) washing of the fabric the dirt and/or soil are removed by dissolution of the sacrificial layer of the polymeric material from the fabric surface. This is also referred to in the art as a secondary cleaning benefit or next-time-cleaning-benefit. Without wishing to be bound by a theory, it is thought that the polymers in the compositions of the invention form a complex when in contact with aqueous solvent 10 under acid conditions by the formation of hydrogen bonds. The complex disperses into an aqueous solvent and does not dissolve, like the individual polymers. The dispersed complex in turn is thought to bind or precipitate onto a fabric surface, thus forming a layer. The complex is thought to disintegrate when in alkaline conditions, such as the conditions in a laundry main wash, thereby removing the layer and soil or 15 stains deposited onto the layer from the fabric. Fabric The fabric that can be treated includes synthetic as well as natural textiles. Fabrics may be made of cotton and other cellulosic materials, polycotton, polyester, silk or 20 nylon. It is envisaged that the method of the present invention can be used to treat garments and other clothing and apparel materials that form typical washload in household laundry. The household materials that can be treated according to the process of the present invention include, but are not limited to, bedspreads, blankets, carpets, curtains and upholstery. Although the process of the present invention is 25 described primarily for treatment of a fabric, it is envisaged that the process of the present invention can be advantageously used to treat other materials such as jute, leather, denim and canvass. It is envisaged that the process of the present invention can be used to treat articles such as shoes, rain-wear and jackets. 30 Polymers WO 2011/026718 PCT/EP2010/061744 7 The composition according to the invention comprises a polymer A and a polymer B. Polymers A and B are selected such that they form a complex due to the formation of hydrogen bonds. 5 The polymers may be homo polymers or co polymers. Wherein by copolymer of monomer X is meant any polymer that contains the monomer X and at least one further monomer. Polymer A 10 According to the present invention, polymer A is a polymer selected from the group of homopolymers and copolymers of carboxylic acid and derivatives. Polymer A has a plurality of carboxyl groups. The polymer A has a molecular mass preferably from 300 to 109 D. The polymer A is selected from the class consisting of homopolymers or copolymers of carboxylic polymers, including natural synthetic and semi-synthetic 15 polymers in this class. Some non-limiting examples of polymer A according to the present invention include: (a) Homopolymer of a carboxylic acid, including but not limited to polycarboxylic acid such as polyacrylic acid, polymaleic acid or copolymer of acrylic and maleic acid. 20 (b) Polysaccharides comprising carboxyl groups. Such poly saccharides may include (but are not limited to) starch, cellulose, sodium alginate, natural gums, and their modified materials such as sodium carboxymethyl cellulose, hydroxyethyl cellulose. Homopolymer or copolymer of carboxylic acid has a molecular mass of preferably 25 from 2x1 03 to 107 D more preferably from 5x1 04 to 106 D and most preferably from 9x10 4 to 5x10 5 D. The particle size is preferably less than 200 im, preferably less than 100 im, more preferably less than 50 im still more preferably less than 10 m, or even less than 30 5pm.

WO 2011/026718 PCT/EP2010/061744 8 The homopolymer or copolymer of saccharide has a molecular mass of preferably from 10 3 to 109 D, more preferably from 10 4 to 109 D and most preferably from 105 to 109 . 5 Polymer A is at least partially neutralised in the Sodium (Nat) form, preferably at least 10%w of polymer A is neutralised, more preferably at least 20%, still more preferably at least 50%. Polymer A may be synthetic, semi-synthetic or natural. However, synthetic or semi 10 synthetic polymers are preferred. Polymer A is preferably water soluble or water dispersible, most preferably polymer A is water soluble. 15 It is preferred that the polymer A is selected from a class consisting of homopolymers or copolymers of carboxylic acid. The homopolymer or copolymer of carboxylic acid is preferably a polyacrylic acid or a copolymer thereof. Examples include SOKALAN@ PA (BASF) and CARBOPOL@ 20 (Lubrizol). The concentration of polymer A in a fabric cleaning or fabric rinse composition is preferably between 0.01 and 25% by weight, more preferably at least 0.1%, or even at least 1%, but preferably not more than 20%, more preferably less than 15%. 25 The amount of polymer A relative to the fabric surface area is preferably from 0.5 to 200 pg/cm 2 of fabric surface area, more preferably from 1 to 100 pg/cm2 , and most preferably from 2 to 50 pg/cm 2 of fabric surface area. The term "fabric surface area" as used herein refers to surface area of one side of the fabric. 30 Polymer B According to the present invention, polymer B has a monomeric unit comprising a group that can form hydrogen bonds with the carboxyl groups of polymer A..

WO 2011/026718 PCT/EP2010/061744 9 Accordingly, polymer B is selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone and/or their derivatives; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose 5 and/or their derivates. The group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose and/or their derivates, is generally not water soluble. In order to obtain the benefit of this group of polymers the particle size is set such that the 10 particles are easily dispersible in water or and aqueous solution (i.e. a wash or rinse liquor). The particle size is preferably less than 200 m, more preferably less than 100 m, even more preferably less than 50 m still more preferably less than 1 O~m, or even less than 5 im. 15 Polymers and homopolymers of carboxylic acid and/or sacchharides and/or polyalkylene glycol/ether qualify to be selected both as polymer A or polymer B, as they comprise hydroxyl or carboxyl group and either a carbonyl or an ether group. However, according to an essential aspect, polymer A and polymer B are not of the same class. It is particularly preferred that the polymers A and B are selected from 20 different classes of polymers. Without wishing to be limited by theory, it is believed that the two polymers A and B, when dissolved in water, form a complex with a solubility lower than each of the polymers A and B, which helps in enhanced deposition and other benefits. 25 Polymer B has a molecular mass preferably from 10 3 to 109 D. Homopolymers or copolymers of vinyl pyrrolidone or vinyl alcohol preferably have a molecular mass of between 103 and 107 D, more preferably from 104 to 106 D and most preferably from 30,000 to 500,000 D. Commercially available polyvinyl 30 pyrrolidone can be used, one example of which is LUVISKOL@ (BASF).

WO 2011/026718 PCT/EP2010/061744 10 Homopolymers or copolymers of poly alkylene oxide preferably have a molecular mass greater than 2x1 04 D. The molecular mass is preferably from 2x1 04 to 106 , more preferably from 3x1 04 to 5x105 D and most preferably from 5x1 04 to 2x105 D. 5 Homopolymers or copolymers of saccharide preferably have a molecular mass of preferably from 103 to 109 D, more preferably from 10 4 to 109 D and most preferably from 10 5 to 10 9 D. Any commercially available poly alkylene oxide, for example POLYOX@ (Dow Chemical Co) can be used according to the present invention. 10 Polymer B may be synthetic, semi-synthetic or natural. However, synthetic or semi synthetic polymers are preferred. According to a preferred aspect, the polymer B is water soluble. 15 It is particularly preferred that the polymer B is selected from a class consisting of homopolymers or copolymers of vinyl pyrrolidone or alkylene oxide. The concentration of polymer B in a fabric cleaning or fabric rinse composition is preferably between 0.01 and 20% by weight, more preferably at least 0.1%, or even at 20 least 1%, but preferably not more than 15%, more preferably less than 10%. The amount of polymer B relative to the fabric surface area is preferably from 0.5 to 200 pg/cm 2 of fabric surface area, more preferably from 1 to 100 pg/cm2 , and most preferably from 2 to 50 pg/cm 2 of fabric surface area. The term "fabric surface area" 25 as used herein refers to surface area of one side of the fabric. Some examples of combinations of polymer A and polymer B, which are particularly preferred, are given below. 30 Table 1: Preferred combination of the polymers Polymer A Polymer B Polyacrylic acid (PAA) Poly vinyl pyrrolidone (PVP) WO 2011/026718 PCT/EP2010/061744 11 Polyacrylic acid (PAA) Polyethylene Oxide(PEO) Polyethylene Glycol (PEG) Polyacrylic acid (PAA) Poly vinyl alcohol (PVA) Polyacrylic acid (PAA) Poly vinyl alcohol (PVA) Polyethylene Oxide (PEO) Sodium carboxymethyl cellulose (SCMC) Polyethylene Oxide (PEO) Hydroxyethyl cellulose Polyacrylic acid(PAA) Starch-graft-polymethacrylic acid Polyethylene Oxide Starch-graft-polymethacrylic acid Polyvinyl pyrrolidone Pluronic-g-Polyacrylic acid Polyethylene Oxide Pluronic-g-Polyacrylic acid Polyvinyl pyrrolidone Sodium carboxymethyl cellulose Hydroxyethyl cellulose Sodium carboxymethyl cellulose Polyvinyl alcohol The most preferred combinations of the polymers are PAA-PVP, PAA-PEO, PEG PAA, Starch-graft-polymethacrylic acid-Polyethylene Oxide. 5 Stabilizers According to one of the preferred embodiment the invention provides a solid fabric treatment composition. In the solid composition the stabilizer is an inorganic alkalinity source. The preferred inorganic alkalinity sources are alkali metal and alkaline earth 10 alkalinity sources. More preferred are alkaline earth oxides and carbonates and alkali metal hydroxides and carbonates. In view of the additional benefit of gas generation, alkali metal and alkaline earth carbonates, e.g. sodium carbonate and potassium carbonate are the most preferred. Polymer A is at least partially neutralised to the salt form by these inorganic alkalinity 15 source. Without wishing to be bound by any particular theory, it is thought that at least partial neutralisation of polymer A to the Sodium form, reduces complex formation during storage and thereby improves the on-shelf stability of the product.

WO 2011/026718 PCT/EP2010/061744 12 According to another preferred embodiment the present invention provides a liquid fabric treatment composition. In the liquid treatment composition the stabilizers are preferably selected from polyvinyl alcohol, silicone, Carboxymethyl cellulose, ethyl cellulose, methyl cellulose, methyl hydroxypropyl cellulose. Alternatively the stabiliser 5 may be selected from surfactants such as anionic, cationic, non-ionic especially ethoxylated fatty alcohols. However these surfactant stabilizers are typically less preferred. If one of the polymers A is polyvinyl alcohol (PVA) then there is no need to add the 10 stabilizer separately. PVA will act both as the polymer A and also as a stabilizer. pH adjustment agent The polymers of the invention are best applied to the fabric at acidic pH and removed at alkaline pH. A normal washing process is done at alkaline pH, generally pH 15 between 8 and 11. When an article is washed under such conditions there will be carry over of some of the high pH (alkaline) washing liquor from the main wash to the rinse step. This carry over is typically in the order of 1:10 and cause the rinse liquor to be alkaline. 20 Therefore the composition of the invention further comprises a pH adjustment agent or a buffer. Suitable pH adjustment agents are, organic and inorganic acids. Such acids are preferably in solid form and have a high water solubility, most preferably they are fully 25 soluble in water. Suitable inorganic acids are boric acid, sodium dihydrogen phosphate, aluminium chloride, aluminium sulphate, cupric sulphate etc. 30 Suitable organic acids in the context of the present invention are citric acid, formic acid, oxalic acid, phtalic acid ascorbic acid, glutamic acid, salicylic acid, tartaric acid, pyroglutamic acid, malic acid, maleic acid, malonic acid, succinic acid, glutaric acid, WO 2011/026718 PCT/EP2010/061744 13 adipic acid, propane 1,2,3 tricarboxylic acid, butane 1,2,3,4 tetra carboxylic acid. The anhydrides of all the abovementioned acids may also be used for this purpose. The wash liquor or rinse liquor wherein the composition of the invention is dissolved, 5 preferably has a pH of less than 6, preferably less than 5 and more preferably less than 4. Aqueous medium has pH preferably greater than 2 and more preferably greater than 3. The polymers may be also chosen in such a way that when the polymers are added to 10 the aqueous medium, pH of the aqueous medium is less than 6. Preferably, an acidic ingredient is added to aqueous medium to ensure that the pH of the aqueous medium is less than 6. Acidic ingredients that reduce pH of resulting aqueous medium to less than 6 are well known to a person skilled in the art and any suitable acidic ingredient may be chosen. 15 Optional ingredients The aqueous medium may comprise an electrolyte. The electrolyte is preferably present in a concentration from 0.001 to 5%, more preferably from 0.01 to 1%, and most preferably from 0.04 to 0.2% by weight of the aqueous medium. 20 Without wishing to be limited by theory, it is believed that the addition of electrolyte allows the process of the invention to be carried out with relatively low amounts of polymers A and B. 25 Electrolytes that can be used according to the present invention include water soluble ionic salts. The cation of the salt includes an alkali metal, alkaline earth metal or trivalent metal cation. The anion of the salt includes chloride, sulphate, nitrate and phosphate. Some examples of electrolytes include chlorides, sulphates or nitrates of sodium, potassium, magnesium or calcium. Calcium salts are particularly preferred. 30 The invention may further comprise natural or synthetic clays, preferably kaolin (kaolinite), bentonite or attapulgate.

WO 2011/026718 PCT/EP2010/061744 14 According to a preferred aspect, the aqueous medium comprises no more than 200 ppm anionic surfactant. The aqueous medium comprises no more than 100 ppm, more preferably less than 50 ppm anionic surfactant. It is particularly preferred that the aqueous medium is substantially free of anionic surfactant. 5 The aqueous medium may further comprise at least one benefit agent. The benefit agent that can be included in the aqueous medium includes, but not limited to ingredients such as perfume, fluorescer, deodorant, antibacterial agent, shading dye and bluing agent. One of the advantages of the present invention is that the 10 deposition of benefit agent is enhanced. Process The composition according to the invention may be applied to a fabric in different ways. 15 One way of applying the composition is by adding the composition to the rinse water of a manual or automatic washing process. The fabric may be added to the rinse water either before or after addition of the composition. Alternatively, the composition may be applied by use of a trigger spray dispenser. 20 In another aspect the invention provides a process for washing fabric comprising the steps in sequence of: contacting the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/I of the solid or liquid composition according to the invention; leaving the fabric to dry; leaving the fabric for soil and/or dirt to deposit onto the fabric; 25 washing the fabric with a conventional washing detergent in a conventional way. The wash liquor preferably comprises at least 0.1g/I of the total solid or liquid composition, more preferably at least 0.25g/l, still more preferably more than 1g/, but typically less than 20g/l, more preferably less than 10 g/l, and even less than 5g/l. 30 The conventional washing process may be any washing process, such as machine wash in an automatic or semi-automatic vertical axis or horizontal axis washing machine or a hand wash process.

WO 2011/026718 PCT/EP2010/061744 15 The detergent may be any conventional washing detergent composition, typically comprising surfactant and builder and optionally perfume, optical brighteners, building aids, etc. 5 Composition The composition comprises preferably 5-95%, more preferably 10-90% and most preferably 20-80% by weight polymer A. The composition comprises preferably 5 95%, more preferably 10-90% and most preferably 20-80% by weight polymer B. 10 The solid composition of the present invention is preferably prepared by first mixing Polymer A with the inorganic alkalinity source to enable at least partial neutralisation even in the solid form; followed by mixing this mixture with the Polymer B and the pH adjustment agent. 15 The liquid composition of the present invention is preferably prepared by first preparing the solution of polymer A and polymer B separately with or without the stabilizer. After that the stabilizer has been added if it is not added while preparing the solution of polymer A and polymer B. Then followed by mixing both solution and 20 stirring it with the pH adjustment agent. For the liquid composition the solvent is selected from water or a mixture of water and lower alcohol. The preferable lower alcohol is selected from methanol, ethanol, iso-propanol etc. The preferred ratio of water to lower alcohol is 6:4 more preferably 9:1 and most preferably 10:0. 25 The polymers may be chosen in such a way that pH of 1% aqueous solution of the composition is less than 6. Preferably, an acidic ingredient is present in the composition at 0.1-10% by weight of the composition to ensure that the pH of 1% aqueous solution of the composition is 30 less than 6. Acidic ingredients that reduce pH of resulting aqueous medium to less than 6 are well known to a person skilled in the art and any suitable acidic ingredient may be chosen.

WO 2011/026718 PCT/EP2010/061744 16 Examples The invention will now be illustrated by means of the following, non-limiting examples. Example 1: Dispersibility of the formulations; Dispersion of polymers by in-situ Gas generation 5 In this example the compositions according to the invention (1 and 2) are compared with comparative compositions outside the scope of the invention, with respect to the required dissolution or dispersion time and the uniformity of the solution or dispersion. 10 For each of the compositions (1, 2 and A-D) 100 ml deionized water was taken in a 250 ml glass beaker and stirred over a magnetic stirrer at controlled speed. The formulation was added to water with continuous stirring and the required time to form a dissolution/dispersion was noted as well as the nature of the dispersion (especially uniformity and/or for lumps remaining). 15 Table 2: dissolution results Comp. Amount Time Remarks (for full (mg / 1OOmI dissolution/dis dispersion) persion) Few lumps A PAA 1 180 >40 min remaining B PAA 180 15 min lumps Sa 30 C PAA 180 >40 lumps Citric Acid 70 D P 180 9 min Clear solution Citric Acid 70 Sa 30 1 PAA 180 >9 min Uniform WO 2011/026718 PCT/EP2010/061744 17 dispersion Citric Acid 70 Sa 30 PEO 3 113 Uniform 2 PAA 1 180 10 min dispersion Citric Acid 70 Sa 30 PEO 113 NaCl 500 1) PAA is polyacrylic acid 2) Soda is Na 2

CO

3 3) PEO is poly ethylene oxide. 5 The table above shows that the compositions according to the invention show fast dissolution and a uniform dispersion of the polymer complex, whilst the comparative compositions A-D show either long dissolution times, or do not show a uniform dispersion. 10 Example 2: Best mode formulations Table 3: best mode solid formulations Example composition 3 (g/I) % PAA 0.15 7.3 PEO 0.10 4.9 Soda 0.15 7.3 NaCl 0.75 37 Citric acid 0.65 32 Kaolin 0.25 12 Total 2.05 100 WO 2011/026718 PCT/EP2010/061744 18 This formulation (example composition 3) gives good dispersion and turbidity in 30 seconds. For polymer coating treatment the cotton, poly cotton and polyester fabric swatches 5 (commercially available from WFK, Germany) were soaked in this dispersion for 30 minutes, and dried in air overnight. The swatches were 10x10 cm. A composite soil was prepared by sonicating a mixture containing 100 ml triolein, 4 10 mg carbon soot and 4 mg iron oxide for 1 hour. A homogeneous soil dispersion was obtained. The fabric swatches were soiled with composite soil and aged for a day at room temperature (ca 24'C). The swatches were then washed in surf XL (ex Unilever) by 15 hand wash procedure. The swatches treated with the composition of Table 2 were completely cleaned by this procedure. 20 Table 4: best mode liquid formulations Composition 9 (Liquid) % wt PAA (100k) 5 PVA(1 25k) 5 PEG (20k) 2.5 Citric Acid 10 Perfume 1 Water to 100 Example 3: Effect of each of the ingredients on cleaning performance In this example a number of compositions according to the invention are compared to 25 comparative compositions.

WO 2011/026718 PCT/EP2010/061744 19 Polymer formulations (as specified in the table below) were prepared according to the method of example 1. The dispersion was checked for lump formation and uniformity. 5 Desized cotton, polycotton and polyester fabric swatches of 10 x 10 cm (cotton, poly cotton and polyester, ex WFK, Germany) were pretreated by soaking into the polymer composition (dispersion) at a liquid to cloth ratio of 5:1 and soaked for 20 minutes. The fabrics used, had a mass of 1.5 g each (i.e. for 100 cm 2 ), resulting in a total of 18.75 pg of total polymer per cm2 of fabric (one side), in the examples where polymer 10 was present. Fabrics were taken out, squeezed out the excess liquor and dried in air. Fabrics were soiled with 0.3 ml of composite soil dispersion (see example 2) applied 15 to about 20 cm2 area and kept for ageing for 16 hours. The fabric swatches were than washed by hand wash, in 1.5 g/l Surf XL wash liquor, at a wash liquor to cloth ratio of 5:1. The fabric swatches were soaked in the liquor for 30 minutes. The soaked fabrics were washed by a handwash protocol by brushing 5 20 times on both side of the fabrics. After brushing the fabrics were rinsed three times with clean water and dried in air. The reflectance of the soil region was measured before and after washing using a reflectometer; the cleaning performance is indicated as the difference ("Delta R") between the reflectance (at 460 nm) before and after washing, as is a commonly known procedure in the art. 25 Control (compositions E and F) Two control examples were included wherein untreated fabric was soiled and washed with Composition E: 3 g/l Surf XL (ex Unilever); and 30 Composition F: 1.5 g/l Surf XL (ex Unilever).

WO 2011/026718 PCT/EP2010/061744 20 3 g/I detergent product is representative for normal hand wash and horizontal axis machine wash. 1.5 g/I is included because the fabrics that are pre-treated with the compositions of the invention are washed with only half of the standard main wash dosage. 5 Comparative compositions (compositions G - M) In comparative examples G-M one or more of the features of the inventions are omitted. 10 Example compositions (4 - 8) Examples 4-8 show compositions according to the invention. Unless otherwise indicated the concentrations in which the ingredients were used were: 15 PAA (poly acrylic acid; Mw 450,000 D, ex Sigma-Aldrich): 0.15 g/l, PEO (poly ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich): 0.10 g/l, NaCl: 0.75 g/l, Perfume: 0.045, Kaolin: 0.25 g/l, Citric acid: 0.2 g/l, Adipic acid: 0.4 g/l, Phthalic anhydride: 0.4 g/l, Soda 0.15 g/I in the pre-treating wash liquor. 20 Table 5: Comparative test results for solid composition Rinse Remarks Cotton Polycotton Polyester Formulation Delta R Delta R Delta R E 3 g/I Surf Excel 14 6 4 F 1.5 g/I Surf Excel 13 5 3 G PAA 0.25 g/I Lumps 14 7 6 Non uniform dispersion No turbidity H PEO 0.25 g/I Lumps 15 4 5 Non uniform dispersion No turbidity I PAA+PEO Lumps 16 5 6 Non uniform dispersion Slight turbidity WO 2011/026718 PCT/EP2010/061744 21 J PAA+PEO+NaCI Lumps remaining 18 6 8 Non uniform dispersion Low turbidity K PAA+PEO+ Lumps remaining 15 5 6 Citric acid Non uniform dispersion No turbidity L PAA+PEO+ Lumps remaining 18 5 7 Citric acid + Non uniform dispersion NaCl M PAA+PEO+ Few very small lumps 15 12 7 Soda+Kaolin Good turbidity 4 PAA+PEO+ Few very small lumps 19 15 9 Citric acid+Soda Good turbidity 5 PAA+PEO+ No lumps 20 17 11 Citric acid+ Uniform dispersion NaCl+ Soda Good turbidity 7 PAA+PEO+ No lumps 22 19 14 Soda+Kaolin+ Uniform dispersion citric acid Good turbidity 8 PAA+PEO+ No lumps 24 21 15 Soda+Kaolin+ Uniform dispersion citric acid+NaCl Good turbidity NB PAA is polyacrylic acid; Soda is Na 2

CO

3 ; PEO is poly ethylene oxide; NaCI is sodium chloride 5 The results in the table above shows that the compositions according to the invention provide substantially better cleaning than the comparative example compositions. Table 6: Comparative test results for liquid composition Rinse Cotton Polycotton Polyester Formulation Delta R Delta R Delta R N Without the 20 10 8 polymer of the composition 9 Composition 9 22 20 17 10 WO 2011/026718 PCT/EP2010/061744 22 The dose of the composition in case to liquid formulation is 2g/lit of rinse liquor. After the fabric treated with the composition of the invention, it is then soiled by composite soil and then usual detergency test was done on the fabric. 5 10 15

Claims

Claims base composition comprising

a mixture of polymer A and a stabilizer wherein the polymer A is selected from the group of homopolymers and copolymers of carboxylic acid and derivatives,

a polymer B selected from

i the group of homopolymers and copolymers of alkylene oxides

having a molecular mass greater than 2x10⁴ D, vinyl pyrrolidone and/or their derivatives; and/or

ii the group of homopolymers and copolymers of vinyl alcohol,

saccharides, hydroxyalkyl cellulose and/or their derivates; and a pH adjustment agent selected from organic acids, selected from citric acid, formic acid, oxalic acid, phtalic acid ascorbic acid, glutamic acid, salicylic acid, tartaric acid, pyroglutamic acid, malic acid, maleic acid, malonic acid, succinic acid, glutaric acid, adipic acid, propane 1 ,2,3 tricarboxylic acid, butane 1 ,2,3,4 tetra carboxylic acid and their anhydides, inorganic acids and/or buffers.

2 A base composition according to claim 1 wherein the pH adjustment agent is an organic acid.

3 A base composition according to claim 1 or 2 wherein the composition further comprises an electrolyte salt or clay or both.

4 A solid fabric treatment composition comprising the base composition as

claimed in any one of the preceding claims wherein the stabilizer is an inorganic alkalinity source.

5 A solid fabric treatment composition as claimed in claim 4 wherein the polymer A is at least partially neutralised to the salt form by reaction with the inorganic alkalinity source. A liquid fabric treatment composition comprising the base composition as claimed in any one of the preceding claims wherein the stabilizer is selected from polyvinyl Alcohol, silicone, carboxymethyl cellulose, ethyl cellulose, methyl cellulose, methyl hydroxypropyl cellulose and surfactants. A liquid fabric treatment composition as claimed in claim 6 wherein the complex of A and B is preformed. A liquid fabric treatment composition as claimed in claim 6 further comprising a solvent. A liquid fabric treatment composition as claimed in claim 7 wherein the solvent is selected from water or a mixture of water and lower alcohol. A composition according to as claimed in any one of the preceding claims wherein Polymer A is present in a concentration of between 0.01 and 25% by weight on the total composition. A composition according to as claimed in any one of the preceding claims wherein Polymer B is present in a concentration of between 0.01 and 20% by weight on the total composition. A wash or rinse liquor comprising between 0.02 and 40 g/l of the composition according to any one of claims 4 to 10, having a pH of < 6 A process for washing fabric comprising the steps in sequence of:

a Contacting the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/l of the composition according to any one of claims 2 to 10; b Leaving the fabric to dry;

c Leaving the fabric for soil and/or dirt to deposit onto the fabric;

d Washing the fabric with a conventional washing detergent in a

conventional way. A process for preparing the solid fabric treatment composition according to the invention comprising the steps of:

a mixing Polymer A with the inorganic alkalinity source; and

b mixing the mixture from step a with the Polymer B and the pH adjustment agent. A process for preparing the liquid fabric treatment composition according to the invention comprising the steps of:

a. Preparing solution of polymer A and polymer B separately with or

without the stabilizer.

b. Adding the stabilizer if it is not added while preparing the solution of polymer A and polymer B.

mixing both solutions and stirring them together with the pH adjustment agent.