WO2011026719A1 - Composition and process for treatment of a fabric - Google Patents
Composition and process for treatment of a fabric Download PDFInfo
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- WO2011026719A1 WO2011026719A1 PCT/EP2010/061745 EP2010061745W WO2011026719A1 WO 2011026719 A1 WO2011026719 A1 WO 2011026719A1 EP 2010061745 W EP2010061745 W EP 2010061745W WO 2011026719 A1 WO2011026719 A1 WO 2011026719A1
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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
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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
- C11D3/02—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
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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
- C11D3/18—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
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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
- C11D3/20—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
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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
- C11D3/3707—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
Definitions
- 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.
- US2006046950A (Penninger and Bastmaschine, 2006) teaches a detergent composition 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.
- 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 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 activity of individual polymers alone when added alone to same detergent compositions.
- 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 nondurable finishes to textiles which impart optimum soil release and soil repellent properties.
- the textiles must be treated with an alkaline aqueous medium having pH value of 7.5-1 1 and containing water soluble hydrophilic soil release polymer having carboxylic acid groups and a dispersed hydrophobic soil repellent fluorochemical.
- 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 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.
- 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.
- 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.
- the present invention provides a fabric treatment composition
- a fabric treatment composition comprising a complex or mixture of a polymer A selected from the group of homopolymers and copolymers of carboxylic acid and derivatives; a spacer compound; and a polymer B selected from the group of homopolymers and
- the present invention provides a wash or rinse liquor 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.
- 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 any one of claims 1 to 5; 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.
- the present invention provides a process for preparing the 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.
- 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.
- 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.
- 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 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.
- the polymers in the 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 laundry main wash, thereby removing the layer and soil or stains deposited onto the layer from the 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 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.
- the process of the present invention is 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.
- 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.
- 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 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 10 9 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.
- 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.
- 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 from 2x10 3 to 10 7 D more preferably from 5x10 4 to 10 6 D and most preferably from 9x10 4 to 5x10 5 D.
- the homopolymer or copolymer of saccharide has a molecular mass of preferably from 10 3 to 10 9 D, more preferably from 10 4 to 10 9 D and most preferably from 10 5 to 10 9 D.
- the particle size is preferably less than 20 ⁇ , more preferably less than ⁇ ⁇ , still more preferably less than 50 ⁇ , even more preferably less than 10 ⁇ , or even less than 5 ⁇ .
- Polymer A may be synthetic, semi-synthetic or natural. However, synthetic or semi- synthetic polymers are preferred.
- Polymer A is preferably water soluble or water dispersable, most preferably polymer A is water soluble.
- 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® (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%.
- the amount of polymer A relative to the fabric surface area is preferably from 0.5 to 200 g/cm 2 of fabric surface area, more preferably from 1 to 100 pg/cm 2 , and most preferably from 2 to 50 g/cm 2 of fabric surface area.
- fabric surface area refers to surface area of one side of the fabric.
- polymer B has a monomeric unit comprising a group that can form hydrogen bonds with the carboxyl groups of polymer A.
- 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, hydroxyalkyi cellulose and/or their derivates.
- the group of homopolymers and copolymers of vinyl alcohol, saccharides, hydroxyalkyi cellulose and/or their derivates, is generally not water soluble.
- 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 200 ⁇ , preferably less than ⁇ ⁇ , more preferably less than 50 ⁇ still more preferably less than 10 ⁇ , or even less than 5 ⁇ .
- 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.
- 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.
- Polymer B has a molecular mass preferably from 10 3 to 10 9 D.
- Homopolymers or copolymers of vinyl pyrrolidone or vinyl alcohol preferably have a molecular mass of between 10 3 and 10 7 D, more preferably from 10 4 to 10 6 D and 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 2x10 4 D.
- the molecular mass is preferably from 2x10 4 to 10 6 D, more preferably from 3x10 4 to 5x10 5 D and most preferably from 5x10 4 to 2x10 5 D.
- Homopolymers or copolymers of saccharide preferably have a molecular mass of preferably from 10 3 to 10 9 D, more preferably from 10 4 to 10 9 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.
- Polymer B may be synthetic, semi-synthetic or natural. However, synthetic or semisynthetic polymers are preferred. According to a preferred aspect, the polymer B is water soluble.
- 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 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
- fabric surface area refers to surface area of one side of the fabric.
- the most preferred combinations of the polymers are PAA-PVP, PAA-PEO, PEG- PAA, Starch-graft-polymethacrylic acid-Polyethylene Oxide.
- the composition further comprises a spacer compound.
- 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).
- 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 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, 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 and limonene.
- Other suitable hydrophobic materials include fatty acids, such as stearic acid; and talc.
- the spacer compounds include both a organic carboxylic acids such as citric acid and also a compound selected from hydrophobic oils or perfumes, due to increased hydrophobicity.
- Inorganic salts are preferably selected from sodium chloride, sodium sulphate, potassium chloride, potassium sulphate, etc
- the invention may further comprise natural or synthetic clays, preferably kaolin
- 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 between 8 and 1 1 .
- alkaline high pH 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.
- the polymers may be chosen in such a way that when the polymers are added to the aqueous medium, pH of the aqueous medium is less than 6.
- 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.
- 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 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.
- 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 acids may also be used for this purpose.
- 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 greater than 3.
- 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.
- 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.
- 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.
- ingredients such as perfume, fluorescer, deodorant, antibacterial agent, shading dye and bluing agent.
- composition according to the invention may be applied to a fabric in different ways.
- 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.
- the composition may be applied by use of a trigger spray dispenser.
- 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/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 way.
- the wash liquor preferably comprises at least 0.1 g/l of the total composition, more preferably at least 0.25g/l, still more preferably more than 1 g/l, but typically less than 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.
- the detergent may be any conventional washing detergent composition, typically comprising surfactant and builder and optionally perfume, optical brighteners, building aids, etc. 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.
- the polymers may be chosen in such a way that pH of 1 % aqueous solution of the composition is less than 6.
- 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 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. Examples
- Example 1 Dispersibility of the formulations
- 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.
- 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).
- Mw 100000 D; ex Sigma-Aldrich.
- 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.
- Example 2 Best mode formulations
- composition 4 (g/i) %
- the cotton, poly cotton and polyester fabric swatches (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 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 hand wash procedure.
- 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.
- Desized cotton, polycotton and polyester fabric swatches of 10 x 10 cm 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 g of total polymer per cm 2 of fabric (one side), in the examples where polymer 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 to about 20 cm 2 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 times on both side of the fabrics. After brushing the fabrics were rinsed three times l o 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.
- Composition E 3 g/l Surf XL (ex Unilever).
- Composition F 1 .5 g/l Surf XL (ex Unilever).
- 3 g/l detergent product is representative for normal hand wash and horizontal axis machine wash. 1 .5 g/l 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.
- compositions G - O Comparative compositions (compositions G - O)
- Examples 5-17 show compositions according to the invention. Unless otherwise indicated the concentrations in which the ingredients were used were:
- PAA poly acrylic acid; Mw 450,000 D, ex Sigma-Aldrich
- PEO poly ethylene oxide; Mw 100,000 D, ex Sigma-Aldrich
- 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.
- NB PAA is polyacrylic acid
- Soda is Na 2 C0 3
- PEO is poly ethylene oxide
- NaCI is sodium chloride
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10741976A EP2473589A1 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
AU2010291393A AU2010291393B2 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
BR112012004224A BR112012004224A2 (en) | 2009-09-02 | 2010-08-12 | wash or rinse water treatment fabric composition, fabric wash process and composition preparation process |
EA201200400A EA201200400A1 (en) | 2009-09-02 | 2010-08-12 | METHOD AND COMPOSITION FOR FABRIC TREATMENT |
CA2771140A CA2771140A1 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
MX2012002747A MX2012002747A (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric. |
CN2010800391429A CN102482617A (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
ZA2012/00793A ZA201200793B (en) | 2009-09-02 | 2012-02-01 | Composition and process for treatment of a fabric |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2006/MUM/2009 | 2009-09-02 | ||
IN2006MU2009 | 2009-09-02 | ||
EP09173675.1 | 2009-10-21 | ||
EP09173675 | 2009-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011026719A1 true WO2011026719A1 (en) | 2011-03-10 |
Family
ID=42937134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2010/061745 WO2011026719A1 (en) | 2009-09-02 | 2010-08-12 | Composition and process for treatment of a fabric |
Country Status (11)
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) |
WO (1) | WO2011026719A1 (en) |
ZA (1) | ZA201200793B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013092184A1 (en) * | 2011-12-20 | 2013-06-27 | Unilever N.V. | Fabric treatment composition |
WO2014079662A1 (en) | 2012-11-21 | 2014-05-30 | Unilever N.V. | Fabric treatment composition |
EP3385333A4 (en) * | 2015-12-01 | 2018-11-21 | Ricoh Company, Ltd. | Water-disintegrable resin composition, and three-dimensional modeling material set and method for producing three-dimensional model using same |
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GB994353A (en) | 1960-06-13 | 1965-06-02 | Domestos Ltd | Improvements in detergent compositions |
GB1333803A (en) | 1970-07-27 | 1973-10-17 | Gaf Corp | Detergent composition and a process for treating textile material |
US4007305A (en) | 1974-12-23 | 1977-02-08 | Basf Wyandotte Corporation | Method of imparting nondurable soil release and soil repellency properties to textile materials |
EP0256696A1 (en) | 1986-07-30 | 1988-02-24 | Unilever Plc | Detergent composition |
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 |
US20060046950A1 (en) | 2003-02-10 | 2006-03-02 | Josef Penninger | Enhancement of the cleaning performance of laundry detergents by cellulose derivative and hygroscopic polymer |
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GB2398792A (en) * | 2003-02-22 | 2004-09-01 | Reckitt Benckiser Inc | Acidic hard surface cleaning and/or disinfecting composition |
RU2473724C2 (en) * | 2007-12-14 | 2013-01-27 | Юнилевер Н.В. | Method of textile processing |
-
2010
- 2010-08-12 EP EP10741976A patent/EP2473589A1/en not_active Withdrawn
- 2010-08-12 MX MX2012002747A patent/MX2012002747A/en not_active Application Discontinuation
- 2010-08-12 CA CA2771140A patent/CA2771140A1/en not_active Abandoned
- 2010-08-12 CN CN2010800391429A patent/CN102482617A/en active Pending
- 2010-08-12 AU AU2010291393A patent/AU2010291393B2/en not_active Ceased
- 2010-08-12 WO PCT/EP2010/061745 patent/WO2011026719A1/en active Application Filing
- 2010-08-12 BR BR112012004224A patent/BR112012004224A2/en not_active IP Right Cessation
- 2010-08-12 EA EA201200400A patent/EA201200400A1/en unknown
- 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 (10)
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GB994353A (en) | 1960-06-13 | 1965-06-02 | Domestos Ltd | Improvements in detergent compositions |
GB1333803A (en) | 1970-07-27 | 1973-10-17 | Gaf Corp | Detergent composition and a process for treating textile material |
US3771951A (en) | 1970-07-27 | 1973-11-13 | Gaf Corp | Improved process for washing polyester materials |
US4007305A (en) | 1974-12-23 | 1977-02-08 | Basf Wyandotte Corporation | Method of imparting nondurable soil release and soil repellency properties to textile materials |
EP0256696A1 (en) | 1986-07-30 | 1988-02-24 | Unilever Plc | Detergent composition |
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 |
US20060046950A1 (en) | 2003-02-10 | 2006-03-02 | Josef Penninger | Enhancement of the cleaning performance of laundry detergents by cellulose derivative and hygroscopic polymer |
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 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013092184A1 (en) * | 2011-12-20 | 2013-06-27 | Unilever N.V. | Fabric treatment composition |
CN103998595A (en) * | 2011-12-20 | 2014-08-20 | 荷兰联合利华有限公司 | Fabric treatment composition |
WO2014079662A1 (en) | 2012-11-21 | 2014-05-30 | Unilever N.V. | Fabric treatment composition |
EP3385333A4 (en) * | 2015-12-01 | 2018-11-21 | Ricoh Company, Ltd. | Water-disintegrable resin composition, and three-dimensional modeling material set and method for producing three-dimensional model using same |
Also Published As
Publication number | Publication date |
---|---|
CA2771140A1 (en) | 2011-03-10 |
BR112012004224A2 (en) | 2016-03-29 |
CL2012000536A1 (en) | 2012-10-19 |
CN102482617A (en) | 2012-05-30 |
EP2473589A1 (en) | 2012-07-11 |
MX2012002747A (en) | 2012-04-19 |
AR078242A1 (en) | 2011-10-26 |
ZA201200793B (en) | 2013-05-29 |
EA201200400A1 (en) | 2012-08-30 |
AU2010291393A1 (en) | 2012-02-23 |
AU2010291393B2 (en) | 2013-07-11 |
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