AU2010291393B2 - Composition and process for treatment of a fabric - Google Patents
Composition and process for treatment of a fabric Download PDFInfo
- Publication number
- AU2010291393B2 AU2010291393B2 AU2010291393A AU2010291393A AU2010291393B2 AU 2010291393 B2 AU2010291393 B2 AU 2010291393B2 AU 2010291393 A AU2010291393 A AU 2010291393A AU 2010291393 A AU2010291393 A AU 2010291393A AU 2010291393 B2 AU2010291393 B2 AU 2010291393B2
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- Australia
- Prior art keywords
- fabric
- polymer
- composition
- group
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000004744 fabric Substances 0.000 title claims abstract description 90
- 239000000203 mixture Substances 0.000 title claims abstract description 86
- 238000000034 method Methods 0.000 title claims abstract description 34
- 230000008569 process Effects 0.000 title claims abstract description 28
- 238000011282 treatment Methods 0.000 title abstract description 15
- 229920000642 polymer Polymers 0.000 claims abstract description 88
- -1 spacer compound Chemical class 0.000 claims abstract description 12
- 239000006185 dispersion Substances 0.000 claims description 37
- 229920001577 copolymer Polymers 0.000 claims description 28
- 229920001519 homopolymer Polymers 0.000 claims description 27
- 238000005406 washing Methods 0.000 claims description 24
- 239000002689 soil Substances 0.000 claims description 20
- 239000003599 detergent Substances 0.000 claims description 15
- 230000002378 acidificating effect Effects 0.000 claims description 11
- 230000002209 hydrophobic effect Effects 0.000 claims description 11
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 8
- 150000001720 carbohydrates Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 6
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- 239000003921 oil Substances 0.000 claims description 6
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- 150000008064 anhydrides Chemical class 0.000 description 11
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- 239000002253 acid Substances 0.000 description 10
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- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 5
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
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- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
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- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
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- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- ODHCTXKNWHHXJC-GSVOUGTGSA-N Pyroglutamic acid Natural products OC(=O)[C@H]1CCC(=O)N1 ODHCTXKNWHHXJC-GSVOUGTGSA-N 0.000 description 2
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- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
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- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 229940117972 triolein Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3715—Polyesters or polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/046—Salts
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/1266—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/18—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3753—Polyvinylalcohol; Ethers or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3776—Heterocyclic compounds, e.g. lactam
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Molecular Biology (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Lubricants (AREA)
- Fats And Perfumes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
The present invention relates to a process for treatment of a fabric. It further relates to 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. It is an object of the present invention is to provide a process for treatment of a fabric that improves efficacy of subsequent cleaning. Surprisingly it is found that a mixture of two (or more) complex forming polymers, wherein one of the polymers is shielded from the other(s) by a spacer compound, solves the problem of stability, while providing the desired cleaning benefit.
Description
WO 2011/026719 PCT/EP2010/061745 1 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 Any discussion of the prior art throughout the specification should in no way be 10 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 detergent research for decades. However, since the present day consumer has ever 15 higher demands for the effectiveness of washing detergents, substantial improvements remain to be desired. US2006046950A (Penninger and Bastigkeit, 2006) teaches a detergent composition for cleaning textile materials comprising a combination of a soil release-capable alkyl 20 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. The use of the hygroscopic polymers in combination with the 25 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 detergent composition. 30 H:\lntrw \NRPortbl\DCC\LGL\5225275_ ldoc.606/2013 -2 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 activity of individual polymers alone when added alone to same detergent compositions. 5 US3771951 (Berni et al, 1973) and GB133803 (Gaf Corp, 1973) teach that detergent 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. 10 The above methods are reported to provide improved antiredeposition of soils and 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. 15 US4007305 (Kakar et al, 1977) addresses the problem of providing satisfactory 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 20 having carboxylic acid groups and a dispersed hydrophobic soil repellent fluorochemical. 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, 25 are relatively difficult to practice in household. In view of the shortcomings of the prior art, the present invention seeks to provide a process for reducing soiling of fabrics that can be easily used in the household.
H: \g\lne v\NRPortbl\DCC\LGL\5225275_I d&c62013 -3 The present invention also seeks to provide a process of treatment of a fabric for reducing soiling of fabrics. The present invention also seeks to provide a process for treatment of a fabric that 5 improves efficacy of subsequent cleaning. The present invention also seeks to provide a process for reducing soiling of fabrics that allows enhanced deposition of benefit agents, such as perfume and fluorescer. 10 The present invention also seeks to provide a process for treatment of a fabric which is effective on various types of fabrics such as cotton, polyester and polycotton. The present invention also seeks to provide a process for treatment of a fabric which is relatively easy to practice in household. 15 The present invention also seeks to provide such a composition and process for easier cleaning in the form of a single product having good storage stability. Surprisingly it is found that a mixture of two (or more) complex forming polymers, wherein 20 one of the polymers is shielded from the other(s) by a spacer compound, solves the problem of stability, while providing the desired cleaning benefit. 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 25 deposition of benefit agents. Summary of the invention G2010 (V) replacement sheets 4 According to a first aspect the present invention provides a process for washing fabric comprising the steps in sequence of: depositing the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/l of the composition comprising a complex of a 5 polymer A selected from the group of homopolymers and copolymers of carboxylic acid; a spacer compound; and a polymer B selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone ; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose; and wherein the composition is in the form of a uniform dispersion and wherein polymer A and polymer B 10 are not of the same class; 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 way. According to a second aspect the present invention provides a wash or rinse liquor 5 comprising between 0.02 and 40 g/l of the composition according to any one of claims 1 to 5, having a pH of < 6. According to a third aspect the present invention provides a process for preparing the !0 composition according to the invention comprising the steps of mixing Polymer A with the spacer compound; and mixing the mixture from step a with the Polymer B.
H:\Une-oenm\NRPortbl\DCC"tCL\s225275_ Lc -66W2013 - 4A By stability of the formulation, it is meant that the complex formation of the interacting polymers is avoided when it is solid form and give an instant complex when dispersed in water. 5 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. 10 According to a further aspect, the present invention provides a process for washing fabric comprising the steps in sequence of: 1. contacting the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/I of a composition comprising: a. a complex of: 15 i. a polymer A selected form the group of homopolymers and copolymers of carboxylic acid; ii. a spacer compound selected from the group of hydrophobic acidic organic compounds, the group of hydrophobic oils, the group of inorganic salts and/or the group of clays; and 20 b. a polymer B selected from: i. the group of homopolymers and copolymers of alkylene oxides having a molecular mass greater than 2x1 0 4 D, vinyl pyrrolidone; and/or ii. the group of homopolymers and copolymers of vinyl alcohol, 25 saccharides, hydroxyalkyl cellulose; and wherein the composition is in the form of a uniform dispersion and wherein polymer A and polymer B are not of the same class; II. leaving the fabric to dry; Ill. leaving the fabric for soil and/or dirt to deposit onto the fabric; 30 IV. washing the fabric with a conventional washing detergent in a conventional way. 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 WO 2011/026719 PCT/EP2010/061745 5 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. 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 5 percentages are weight/weight percentages unless otherwise indicated. Numerical ranges expressed in the format "from x to y" are understood to include x and y. When for a specific feature multiple preferred ranges are described in the format "from x to y", it is understood that all ranges combining the different endpoints are also contemplated. 10 Detailed description of the invention The present invention thus aims for a composition 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 (conventional) washing of the fabric 15 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 20 compositions of the invention form a complex when in contact with water under acid conditions by the formation of hydrogen bonds. The complex disperses into water 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 25 laundry main wash, thereby removing the layer and soil or stains deposited onto the layer from the fabric. Fabric The fabric that can be treated includes synthetic as well as natural textiles. Fabrics 30 may be made of cotton and other cellulosic materials, polycotton, polyester, silk or 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 G201 0 (V) replacement sheets 6 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 5 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. 10 Polymers 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 at least one further monomer. Polymer A 0 According to the present invention, polymer A is a polymer selected from the group of homopolymers and copolymers of carboxylic acid . 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 polymers in this class. 5 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. (b) Polysaccharides comprising carboxyl groups. Such poly saccharides may include 0 (but are not limited to) starch, cellulose, sodium alginate, natural gums, and their modified materials such as sodium carboxymethyl cellulose, hydroxyethyl cellulose.
WO 2011/026719 PCT/EP2010/061745 7 Homopolymer or copolymer of carboxylic acid has a molecular mass of preferably from 2x1 03 to 107 D more preferably from 5x1 04 to 106 D and most preferably from 9x10 4 to 5x10 5 D. 5 The homopolymer or copolymer of saccharide has a molecular mass of preferably from 103 to 109 D, more preferably from 104 to 109 D and most preferably from 105 to 109 D. 10 The particle size is preferably less than 200 tm, more preferably less than 100 tm, still more preferably less than 50 tm, even more preferably less than 10 m, or even less than 5 tm. Polymer A may be synthetic, semi-synthetic or natural. However, synthetic or semi 15 synthetic polymers are preferred. Polymer A is preferably water soluble or water dispersable, most preferably polymer A 20 is water soluble. It is preferred that the polymer A is selected from a class consisting of homopolymers or copolymers of carboxylic acid. 25 The homopolymer or copolymer of carboxylic acid is preferably a polyacrylic acid or a copolymer thereof. Examples include SOKALAN@ PA (BASF) and CARBOPOL@ (Lubrizol). The concentration of polymer A in a fabric cleaning or fabric rinse composition is 30 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%.
G201 0 (V) replacement sheets 8 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/cm 2 , and most preferably from 2 to 50 pg/cm 2 of fabric surface area. The term "fabric surface area" as 5 used herein refers to surface area of one side of the fabric. 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. I0 Accordingly, polymer B is selected from the group of homopolymers and copolymers of alkylene oxides, vinyl pyrrolidone; and/or the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose. 5 The group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose, is generally not water soluble. In order to obtain the benefit of this group of polymers the particle size is set such that the particles are easily dispersible in water or and aqueous solution (i.e. a wash or rinse liquor). The particle size is preferably less than 200pm, preferably less than 10sm, more preferably less than 50pm still more 0 preferably less than I 0pm, or even less than 5pm. 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 5 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 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.
WO 2011/026719 PCT/EP2010/061745 9 Polymer B has a molecular mass preferably from 103 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 5 most preferably from 30,000 to 500,000 D. Commercially available polyvinyl pyrrolidone can be used, one example of which is LUVISKOL@ (BASF). 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 D, 10 more preferably from 3x1 04 to 5x105 D and most preferably from 5x1 04 to 2x105 D. Homopolymers or copolymers of saccharide preferably have a molecular mass of preferably from 103 to 109 D, more preferably from 104 to 109 D and most preferably from 105 to 109 D. Any commercially available poly alkylene oxide, for example 15 POLYOX@ (Dow Chemical Co) can be used according to the present invention. Polymer B may be synthetic, semi-synthetic or natural. However, synthetic or semi synthetic polymers are preferred. 20 According to a preferred aspect, the polymer B is water soluble. It is particularly preferred that the polymer B is selected from a class consisting of homopolymers or copolymers of vinyl pyrrolidone or alkylene oxide. 25 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 least 1%, but preferably not more than 15%, more preferably less than 10%. 30 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/cm 2 , and most G2010 (V) replacement sheets 10 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. 5 Some examples of combinations of polymer A and polymer B, which are particularly preferred, are given below. Table 1: Preferred combination of the Polymers Polymer A Polymer B Polyacrylic acid (PAA) Poly vinyl pyrrolidone (PVP) Polyacrylic acid (PAA) Polyethylene Oxide(PEO) Polyacrylic acid (PAA) Polyethylene Glycol (PEG) Polyacrylic acid (PAA) Poly vinyl alcohol (PVA) Sodium carboxymethyl cellulose (SCMC) Polyethylene Oxide (PEO) Polyacrylic acid(PAA) Hydroxyethyl cellulose 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 0 The most preferred combinations of the polymers are PAA-PVP, PAA-PEO, PEG-PAA, Starch-graft-polymethacrylic acid-Polyethylene Oxide. Spacer compound The composition further comprises a spacer compound. Without wishing to be bound to 5 any particular theory, it is thought that the use of a spacer compound of the invention improves the storage stability of the composition as it reduces complex forming on storage, while at the same time it improves the dispersibility of the composition when brought in contact with water (or an aqueous solution).
WO 2011/026719 PCT/EP2010/061745 11 The spacer compound of the present invention is preferably selected from the group of hydrophobic acidic organic compounds, the group of hydrophobic oils, the group of inorganic salts and/or the group of clays. The compositions according to the invention comprise at least one spacer compound, but preferably two or more, more preferably 5 even 3 or more. When two or more spacer compounds are present, it is most preferred that they are chosen from different groups. Hydrophobic acidic organic compounds are preferably selected from phtalic acid, phthalic anhydride, ascorbic acid, glutamic acid, salicylic acid, tartaric acid, 10 pyroglutamic acid, malic acid, maleic acid, malonic acid, succinic acid, glutarric acid, 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. Hydrophobic oils are preferably selected from perfume ingredients, e.g. perfume oils 15 and limonene. Other suitable hydrophobic materials include fatty acids, such as stearic acid; and talc. Even better dispersions may be obtained when the spacer compounds include both a organic carboxylic acids such as citric acid and also a compound selected from 20 hydrophobic oils or perfumes, due to increased hydrophobicity. Inorganic salts are preferably selected from sodium chloride, sodium sulphate, potassium chloride, potassium sulphate, etc 25 The invention may further comprise natural or synthetic clays, preferably kaolin (kaolinite), bentonite or attapulgate. pH adjustment agent The polymers of the invention are best applied to the fabric at acidic pH and removed 30 at alkaline pH. A normal washing process is done at alkaline pH, generally pH 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 WO 2011/026719 PCT/EP2010/061745 12 rinse step. This carry over is typically in the order of 1:10 and cause the rinse liquor to be alkaline. The polymers may be chosen in such a way that when the polymers are added to the 5 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. 10 However, the composition of the invention may further comprise a pH adjustment agent or a buffer. Suitable pH adjustment agents are, organic and inorganic acids. Such acids are 15 preferably in solid form and have a high water solubility, most preferably they are fully soluble in water. Suitable inorganic acids are boric acid, sodium dihydrogen phosphate, aluminium chloride, aluminium sulphate, cupric sulphate etc. 20 Suitable organic acids 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, adipic acid, propane 1,2,3 tricarboxylic acid, butane 1,2,3,4 tetra carboxylic acid. The anhydrides of all the abovementioned 25 acids may also be used for this purpose. The wash liquor or rinse liquor wherein the composition of the invention is dissolved, 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 30 greater than 3.
WO 2011/026719 PCT/EP2010/061745 13 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. 5 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. 10 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. 15 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. 20 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 25 deposition of benefit agent is enhanced. Process The composition according to the invention may be applied to a fabric in different ways. 30 WO 2011/026719 PCT/EP2010/061745 14 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. 5 Alternatively, the composition may be applied by use of a trigger spray dispenser. 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 composition according to the invention; leaving the 10 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 way. The wash liquor preferably comprises at least 0.1g/I of the total composition, more preferably at least 0.25g/l, still more preferably more than 1g/l, but typically less than 15 20g/l, more preferably less than 10 g/l, and even less than 5g/l. 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. 20 The detergent may be any conventional washing detergent composition, typically comprising surfactant and builder and optionally perfume, optical brighteners, building aids, etc. 25 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. 30 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% WO 2011/026719 PCT/EP2010/061745 15 aqueous solution of the composition 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. 5 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 10 In this example the compositions according to the invention (1 - 3) 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. 15 For each of the compositions (1-3 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). 20 Table 2: dissolution results Comp Amount Time Remarks (mg / 100ml (for full dispersion) dissolution/ dispersion) A PAA 180 > 40 min Lumps remaining B PAA 180 > 40 min Few lumps remaining Perfume 30 C PAA 180 > 20 min Lumps remaining Phthalic 70 anhydride D PAA 180 > 10 min Good solution Phthalic 70 anhydride Perfume 30 1 PAA 180 8 min Good Dispersion Phthalic 70 WO 2011/026719 PCT/EP2010/061745 16 anhydride Perfume 30 PEO 113 2 PAA 180 7 min Uniform dispersion Phthalic 70 anhydride Perfume 30 PEO 113 NaCl 500 3 PAA 180 7 min Uniform dispersion Phthalic 70 anhydride Perfume 30 PEO 113 Kaolin 500 NB PAA is polyacrylic acid (Mw = 450000 D; ex Sigma-Aldrich) Soda is Na 2
CO
3 PEO is poly ethylene oxide (Mw = 100000 D; ex Sigma-Aldrich). 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 formulations Composition 4 (gI) % PAA 0.15 9 PEO 0.10 6 Phtahlic anhydride 0.40 24 Perfume 0.044 3 NaCI 0.75 44 Kaolin 0.25 15 Total 1.69 100 WO 2011/026719 PCT/EP2010/061745 17 This formulation (example composition 4) 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 mg carbon soot and 4 mg iron oxide for 1 hour. A homogeneous soil dispersion was 10 obtained. The fabric swatches were soiled with composite soil and aged for a day at room temperature (ca 240C). The swatches were then washed in surf XL (ex Unilever) by hand wash procedure. 15 The swatches treated with the composition of Table 2 were completely cleaned by this procedure. Example 3: Effect of each of the ingredients on cleaning performance 20 In this example a number of compositions according to the invention are compared to comparative compositions. 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. 25 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 30 18.75 pg of total polymer per cm2 of fabric (one side), in the examples where polymer was present.
WO 2011/026719 PCT/EP2010/061745 18 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 to about 20 cm 2 area and kept for ageing for 16 hours. 5 The fabric swatches were than washed by hand wash, in 1.5 g/I 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 times on both side of the fabrics. After brushing the fabrics were rinsed three times 10 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. 15 Control (compositions E and F) Two control examples were included wherein untreated fabric was soiled and washed with Composition E: 3 g/I Surf XL (ex Unilever); and Composition F: 1.5 g/I Surf XL (ex Unilever). 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. 25 Comparative compositions (compositions G - 0) In comparative examples G-O one or more of the features of the inventions are omitted. 3 0 Example compositions (5 - 17) Examples 5-17 show compositions according to the invention.
WO 2011/026719 PCT/EP2010/061745 19 Unless otherwise indicated the concentrations in which the ingredients were used were: PAA (poly acrylic acid; Mw 450,000 D, ex Sigma-Aldrich): 0.15 g/l, PEO (poly 5 ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich): 0.10 g/l, NaCI: 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/l in the pre-treating wash liquor. Table 4: Comparative test results Rinse Formulation Remarks Cotton Poly- Poly cotton ester Delta R Delta R Delta R E Control 3 g/Il 14 6 4 F Control 1.5 g/l 13 5 3 G PAA 0.25 g/l Lumps Non uniform 14 7 6 dispersion No turbidity H PEO 0.25 g/l Lumps Non uniform 15 4 5 dispersion No turbidity I PAA+PEO 0.25 g/l Lumps 16 5 6 Non uniform dispersion Slight turbidity J PAA+PEO+NaCI Lumps remaining 18 6 8 Non uniform dispersion Low turbidity K PAA+PEO+Citric Lumps remaining 15 5 6 acid Non uniform dispersion No turbidity L PAA+PEO+Citric Lumps remaining 18 5 7 acid/NaCl Non uniform dispersion M PAA+Phthalic Lumps remaining 14 7 5 anhydride Slight Turbidity N PEO+Phthalic Lumps remaining 15 5 4 anhydride Slight Turbidity o PEO+Phthalic Lumps remaining 15 6 5 anhydride+NaCI Slight Turbidity 5 PAA+PEO+Citric No lumps 18 10 9 Acid+Perfume Uniform dispersion Good turbidity 6 PAA+PEO+ Uniform dispersion 19 15 16 Citric Acid+NaCl+ Good turbidity WO 2011/026719 PCT/EP2010/061745 20 Perfume 7 PAA+PEO+ Uniform dispersion 19 10 6 Citric acid+NaCl+ Good turbidity Kaolin+Perfume 8 PAA+PEO+ Few very small 16 18 16 Phthalic anhydride lumps Turbidity develops slowly 9 PAA+PEO+ Few very small 17 19 17 Phthalic anhydride+ lumps NaCl Turbidity develops slowly 10 PAA+PEO+ Few very small 17 18 16 Phthalic anhydride+ lumps Turbidity Kaolin develops slowly 11 PAA+PEO+ Uniform dispersion 18 18 16 Phthalic anhydride+ Good turbidity NaCI+Kaolin 12 PAA+PEO+ Few very small 17 19.5 21 Phthalic anhydride+ lumps Perfume Good turbidity 13 PAA+PEO+ No lumps 17 19 18 Phthalic anhydride+ Uniform dispersion Perfume+NaCI Good turbidity 14 PAA+PEO+ Uniform dispersion 18 20 19 Phthalic anhydride+ Good turbidity Perfume+Kaolin 15 PAA+PEO+ Uniform dispersion 19 21 20 Phthalic anhydride+ Good turbidity Perfume+NaCl+ Kaolin 16 PAA+PEO+ Uniform dispersion 19 16 18 Adipic acid+ Good turbidity Perfume+NaCl 17 PAA+PEO+ Uniform dispersion 19 21 20 Adipic acid+ Good turbidity Perfume+NaCl+ Kaolin _ _ _ _ _ _ NB PAA is polyacrylic acid; Soda is Na 2
CO
3 ; PEO is poly ethylene oxide; NaCI is sodium chloride The results in the table above shows that the compositions according to the invention 5 provide substantially better cleaning than the comparative example compositions.
H:U\glntcr e\NRPorthI\DCC\LGL\5225275_I.doc-66/2013 - 20A Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. 5 The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as, an acknowledgement or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of 10 endeavour to which this specification relates.
Claims (5)
1. A process for washing fabric comprising the steps in sequence of: 1. contacting the fabric with a wash or rinse liquor comprising between 0.02 and 40 g/l of a composition comprising a. a complex of i. a polymer A selected from the group of homopolymers and copolymers of carboxylic acid; ii. a spacer compound selected from the group of hydrophobic acidic organic compounds, the group of hydrophobic oils, the group of inorganic salts and/or the group of clays; and b. a polymer B selected from i. the group of homopolymers and copolymers of alkylene oxides having a molecular mass greater than 2x10 4 D, vinyl pyrrolidone; and/or ii. the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyl cellulose; and wherein the composition is in the form of a uniform dispersion and wherein polymer A and polymer B are not of the same class; II. leaving the fabric to dry; Ill. leaving the fabric for soil and/or dirt to deposit onto the fabric; IV. washing the fabric with a conventional washing detergent in a conventional way.
2. A process according to claim 1, wherein Polymer A is present in a concentration of between 0.01 and 25% by weight on the total composition.
3. A process according to any one of claims 1 or 2, wherein Polymer B is present in a concentration of between 0.01 and 20% by weight on the total composition. 22
4. A process according to any one of the preceding claims, comprising two or more spacer compounds.
5. A process according to any one of the preceding claims, wherein the wash or rinse liquor has a pH of < 6.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2006MU2009 | 2009-09-02 | ||
| IN2006/MUM/2009 | 2009-09-02 | ||
| EP09173675 | 2009-10-21 | ||
| EP09173675.1 | 2009-10-21 | ||
| PCT/EP2010/061745 WO2011026719A1 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
Publications (2)
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| AU2010291393A1 AU2010291393A1 (en) | 2012-02-23 |
| AU2010291393B2 true AU2010291393B2 (en) | 2013-07-11 |
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| AU2010291393A Ceased AU2010291393B2 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP2473589A1 (en) |
| CN (1) | CN102482617A (en) |
| AR (1) | AR078242A1 (en) |
| AU (1) | AU2010291393B2 (en) |
| BR (1) | BR112012004224A2 (en) |
| CA (1) | CA2771140A1 (en) |
| CL (1) | CL2012000536A1 (en) |
| EA (1) | EA201200400A1 (en) |
| MX (1) | MX2012002747A (en) |
| PH (1) | PH12012500256A1 (en) |
| WO (1) | WO2011026719A1 (en) |
| ZA (1) | ZA201200793B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| BR112014015521A8 (en) * | 2011-12-20 | 2017-07-04 | Unilever Nv | fabric treatment composition, fabric treatment process and fabric softener |
| ES2645446T3 (en) | 2012-11-21 | 2017-12-05 | Unilever N.V. | Fabric treatment composition |
| CN108368351A (en) * | 2015-12-01 | 2018-08-03 | 株式会社理光 | Water-destructible property resin combination and use its three-dimensional modeling material group and three-D moulding object manufacturing method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030186832A1 (en) * | 2002-03-15 | 2003-10-02 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Isotropic liquid detergents with improved anti-redeposition |
| WO2003099981A1 (en) * | 2002-05-23 | 2003-12-04 | The Procter & Gamble Company | Methods and articles for reducing airborne particulates |
| GB2398571A (en) * | 2003-02-22 | 2004-08-25 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
| DE10331053A1 (en) * | 2003-07-09 | 2005-01-27 | Basf Ag | Additives e.g. for use in surface modifiers, detergents or textile lubricants comprise a vinyl acetate/methacrylic or crotonic acid hydrophobic copolymer and a cation modifier |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB994353A (en) | 1960-06-13 | 1965-06-02 | Domestos Ltd | Improvements in detergent compositions |
| US3689435A (en) | 1970-07-27 | 1972-09-05 | Gaf Corp | Detergency compositions containing a synergistic mixture of pvp and pva |
| US4007305A (en) | 1974-12-23 | 1977-02-08 | Basf Wyandotte Corporation | Method of imparting nondurable soil release and soil repellency properties to textile materials |
| GB8618635D0 (en) | 1986-07-30 | 1986-09-10 | Unilever Plc | Detergent composition |
| ATE363525T1 (en) | 2003-02-10 | 2007-06-15 | Henkel Kgaa | INCREASING THE CLEANING PERFORMANCE OF DETERGENTS THROUGH CELLULOSE DERIVATIVE AND HYGROSCOPIC POLYMER |
| GB2398792A (en) * | 2003-02-22 | 2004-09-01 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
| JP5080652B2 (en) * | 2007-12-14 | 2012-11-21 | ユニリーバー・ナームローゼ・ベンノートシヤープ | How to treat the dough |
-
2010
- 2010-08-12 BR BR112012004224A patent/BR112012004224A2/en not_active IP Right Cessation
- 2010-08-12 AU AU2010291393A patent/AU2010291393B2/en not_active Ceased
- 2010-08-12 EP EP10741976A patent/EP2473589A1/en not_active Withdrawn
- 2010-08-12 CA CA2771140A patent/CA2771140A1/en not_active Abandoned
- 2010-08-12 WO PCT/EP2010/061745 patent/WO2011026719A1/en not_active Ceased
- 2010-08-12 EA EA201200400A patent/EA201200400A1/en unknown
- 2010-08-12 PH PH1/2012/500256A patent/PH12012500256A1/en unknown
- 2010-08-12 MX MX2012002747A patent/MX2012002747A/en not_active Application Discontinuation
- 2010-08-12 CN CN2010800391429A patent/CN102482617A/en active Pending
- 2010-09-01 AR ARP100103191A patent/AR078242A1/en not_active Application Discontinuation
-
2012
- 2012-02-01 ZA ZA2012/00793A patent/ZA201200793B/en unknown
- 2012-02-29 CL CL2012000536A patent/CL2012000536A1/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030186832A1 (en) * | 2002-03-15 | 2003-10-02 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Isotropic liquid detergents with improved anti-redeposition |
| WO2003099981A1 (en) * | 2002-05-23 | 2003-12-04 | The Procter & Gamble Company | Methods and articles for reducing airborne particulates |
| GB2398571A (en) * | 2003-02-22 | 2004-08-25 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
| DE10331053A1 (en) * | 2003-07-09 | 2005-01-27 | Basf Ag | Additives e.g. for use in surface modifiers, detergents or textile lubricants comprise a vinyl acetate/methacrylic or crotonic acid hydrophobic copolymer and a cation modifier |
Also Published As
| Publication number | Publication date |
|---|---|
| EA201200400A1 (en) | 2012-08-30 |
| EP2473589A1 (en) | 2012-07-11 |
| ZA201200793B (en) | 2013-05-29 |
| CL2012000536A1 (en) | 2012-10-19 |
| MX2012002747A (en) | 2012-04-19 |
| PH12012500256A1 (en) | 2012-10-22 |
| AU2010291393A1 (en) | 2012-02-23 |
| WO2011026719A1 (en) | 2011-03-10 |
| CN102482617A (en) | 2012-05-30 |
| AR078242A1 (en) | 2011-10-26 |
| CA2771140A1 (en) | 2011-03-10 |
| BR112012004224A2 (en) | 2016-03-29 |
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