EP2031050A1 - Processus de nettoyage de tissus - Google Patents

Processus de nettoyage de tissus Download PDF

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Publication number
EP2031050A1
EP2031050A1 EP07120469A EP07120469A EP2031050A1 EP 2031050 A1 EP2031050 A1 EP 2031050A1 EP 07120469 A EP07120469 A EP 07120469A EP 07120469 A EP07120469 A EP 07120469A EP 2031050 A1 EP2031050 A1 EP 2031050A1
Authority
EP
European Patent Office
Prior art keywords
component
acid
fabric
cleaning
water
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.)
Withdrawn
Application number
EP07120469A
Other languages
German (de)
English (en)
Inventor
Shubhadeep Banerjee
Kaushik Bose
Deeleep Kumar Rout
Ritesh Kumar Sinha
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever NV
Original Assignee
Unilever NV
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unilever NV filed Critical Unilever NV
Publication of EP2031050A1 publication Critical patent/EP2031050A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/06Hydroxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/10Salts
    • C11D7/12Carbonates bicarbonates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/10Salts
    • C11D7/16Phosphates including polyphosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/26Organic compounds containing oxygen
    • C11D7/265Carboxylic acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10Objects to be cleaned
    • C11D2111/12Soft surfaces, e.g. textile
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/40Specific cleaning or washing processes
    • C11D2111/44Multi-step processes

Definitions

  • the invention relates to a process for cleaning fabrics. It particularly relates to a multi-step process for cleaning fabrics.
  • Conventional process of cleaning fabrics is typically a single step process of contacting a fabric with a detergent formulation in presence of water.
  • this process involves soaking fabrics in a soak solution of commercially available detergent formulations in water, followed by washing, and then followed by rinsing to get rid of excess water, dirt and leftover surfactant.
  • the steps of washing and rinsing are usually aided by means of agitation, provided either manually as in hand-wash or mechanically as in machine wash.
  • cleaning performance deteriorates with increase in water hardness, or with decrease in wash temperature.
  • Conventional processes also require longer time and consumption of high quantity of water.
  • GB338121 (1930 ) describes a process of washing by adding together or one after another two components to the wash where the first component comprises saponifiable fatty acids such as oleic acid, palmitic acid, or stearic acid and the second component comprises alkaline saponifying agents such as sodium carbonate, sodium bicarbonate or sodium hydroxide.
  • saponifiable fatty acids such as oleic acid, palmitic acid, or stearic acid
  • alkaline saponifying agents such as sodium carbonate, sodium bicarbonate or sodium hydroxide.
  • the above process involves fatty acids which are not readily soluble in water and solvents are used to solubilize fatty acids to facilitate their uniform application to fabrics.
  • Other approach is use of an emulsifying agent for forming an aqueous emulsion to facilitate uniform application of fatty acids to fabrics.
  • FR1460904 (1966 ) describes a process of washing fabrics in which aqueous emulsion of saponifiable fatty acids is combined with the alkaline wash solution.
  • Fatty acids are preferably selected from oleic acid or low-melting fatty acid mixture and emulsifying agent is a low HLB nonionic surfactant.
  • GB333177 (1930 ) describes a process of washing consisting of successively treating the material to be washed with a dilute emulsion of saponifiable fatty acids and with a dilute alkali to generate soap in-situ.
  • GB501422 (1939 ) describes a process for washing articles with a fatty acid component and an alkali component where the aqueous fatty acid emulsion comprises methyl cyclohexanol.
  • GB2315762 (Procter and Gamble, 1998) describes a detergent composition comprising a detergent surfactant, a dicarboxylic acid source and an alkaline source.
  • Dicarboxylic acid source is selected from fumaric acid, malic acid, maleic acid, tartaric acid, malonic acid, or a salt or ester thereof.
  • EP11767501 (Procter and Gamble, 2002) describes a process of washing a fabric by successively treating the fabric, in any order, with a first component and a second component which are capable of generating heat upon contact.
  • the components are selected such that contact of the components is a part of an exothermic process of either a physical or a chemical nature and results in generation of heat.
  • a list of exothermic processes is given and includes dissolution of organic/inorganic salts, oxidation/reduction, hydration of substantially anhydrous compounds and acid/base reactions.
  • the acids, whether organic or inorganic are preferably strong acids with pKa less than 4, or more preferably less than 2.
  • Preferred organic acids include choloro acetic acid, dichloro acetic acid, acetic acid, oxalic acid, formic acid, lactic acid or mixtures thereof.
  • strong acids which are water soluble helps in eliminating problems related to use of insoluble fatty acids as there is no need to use solvents or emulsifying agents.
  • strong acids are difficult to handle, store and keep out of reach of minors. For consumers who prefer hand-wash, it is particularly problematic to handle strong acids and keep them out of reach of children.
  • packaging of strong acids is another issue which may lead to leaking or may require expensive packaging materials.
  • strong acids such as mineral acids may not be compatible with the material of construction of washing machines. Strong acids may also cause damage to expensive and delicate fabrics or textile accessories like buttons and elastic.
  • one of the objectives of the present invention is to overcome or ameliorate at least one of the disadvantages of the prior art, or to provide a useful alternative.
  • Another object of the present invention is to provide a process for cleaning fabrics which causes relatively less damage to fabrics.
  • Yet another object of the present invention is to provide a process for cleaning fabrics which can be used to effectively remove particulate soils.
  • Yet another object of the present invention is to provide a process for cleaning fabrics which may be carried out in absence of conventional surfactants.
  • a process for cleaning a fabric including the step of contacting the fabric with two components sequentially, in any order, wherein;
  • the pKa of the acid is greater than 4.
  • a process for cleaning a fabric including the step of contacting the fabric with two components sequentially, in any order, wherein;
  • the first component is the first component
  • the first component includes an organic acid that has a molecular weight greater than 200, and has at least two carboxylic acid groups.
  • the organic acid is 0.01-100%, preferably 0.01-10%, more preferably 0.1-5% by weight of the first component.
  • the pKa of the acid is preferably greater than 4, more preferably greater than 4.1 and most preferably greater than 4.5.
  • the molecular weight of the organic acid is preferably greater than 200, more preferably greater than 300, and most preferably greater than 1000. According to a preferred aspect, molecular weight of organic acid is preferably from 200 to 5000000, more preferably from 300 to 4000000, most preferably from 1000 to 1000000.
  • the acid is selected from a polycarboxylic acid or an oligomer of C12-C30 unsaturated fatty acid.
  • Polycarboxylic acid is particularly preferred.
  • polycarboxylic acid has preferably greater than three, more preferably greater than 10, most preferably greater than 25 carboxylic acid groups.
  • Preferred polycarboxylic acids include polyacrylic acid, polymethacrylic acid, polymaleic acid, polyacrylic/polymaleic acid co-polymers, and poly amino acid.
  • Non-limiting examples of poly amino acids include poly gamma glutamic acid and polyaspartic acid. Polyacrylic acid is particularly preferred.
  • organic acid is an oligomer of C12-C30 unsaturated fatty acid.
  • unsaturated fatty acid as used herein means a fatty acid with at least on carbon-carbon double bond.
  • oligomer as used herein refers to a polymer comprising two to five monomer units. A dimer of an unsaturated fatty acid is particularly preferred in the process of the present invention.
  • the organic acid can be water-insoluble or water-soluble.
  • preferred water-insoluble acids include dimer of C12-C30 unsaturated fatty acid.
  • the first component comprises 0-99.99%, preferably 90-99.99%, more preferably 95-99.99% non-aqueous carrier.
  • the non-aqueous carrier preferably comprises solvents capable of dissolving the water-insoluble organic acid. Commonly used organic non-chlorinated and chlorinated solvents can be used. Some non-limiting examples of solvents that can be used according to the present invention include methanol, acetone, chloroform, and dichloromethane. Alternatively, water-insoluble acid may be emulsified in an aqueous medium using an emulsifying agent.
  • organic acid is water-soluble.
  • the first component comprises 0-99.99%, preferably 90-99.99%, more preferably 95-99.99% aqueous carrier.
  • the aqueous carrier preferably comprises water.
  • the aqueous carrier may further comprise conventional detergent ingredients. It is preferred that the conventional detergent ingredients included in the aqueous carrier of the first component are not alkaline.
  • ingredients that can be added with the first component include optical brighteners (e.g., Tinopal® CBSX/Photine®)), electrolytes (e.g., sodium chloride, sodium sulphate, sodium citrate), perfume, and soil release polymers (e.g. sodium carboxymethyl cellulose and Gerol), acid-compatible phosphonic acid builders (methylenephosphonic acid, phosphonobutane tricarboxylic acid).
  • the first component may be a solid, liquid, paste, gel or any other suitable format.
  • the first component is liquid.
  • the second component is the first component
  • the second component includes an alkaline material.
  • the alkaline material according to the present invention includes any material that has an alkaline pH when mixed with water. When mixed with water, the alkaline material has a pH of greater than 7.5, preferably greater than 8.5, more preferably greater than 9 and most preferably greater than 10.
  • Alkaline material can be inorganic or organic.
  • the alkaline material is inorganic.
  • inorganic alkaline material is selected from carbonate, bicarbonate, phosphate or hydroxide of an alkali metal, alkaline earth metal or ammonium.
  • Particularly preferred inorganic alkaline material is selected from carbonate, bicarbonate, phosphate or hydroxide of an alkali metal.
  • sodium is particularly preferred.
  • the most preferred alkaline material is selected from sodium carbonate, sodium tripolyphosphate or mixture thereof.
  • alkaline material is selected from organic bases.
  • organic bases include C1-C10 amines, C1-C10 alkanolamines and urea.
  • the alkaline material is 0.1-100%, preferably 0.1-20%, more preferably 0.1-5% by weight of the second component.
  • the second component includes 0-99.9%, preferably 80-99.9%, more preferably 95-99.9% by weight an aqueous carrier.
  • the aqueous carrier preferably comprises water.
  • the aqueous carrier may further comprise of conventional detergent ingredients. It is preferred that the conventional detergent ingredients included in the aqueous carrier of the second component are not acidic.
  • Conventional detergent ingredients that can be included in the aqueous carrier of the second component include zeolite, co-builders such as CP5, phosphonates such as salts of phosphonobutane tricarboxylic acids, and reductive bleaches such as sodium sulphite.
  • the second component may be used in a solid, liquid, paste, gel or any other suitable format. According to one of the preferred aspect the second component is used in the solid form.
  • Either of the components may include a surfactant conventionally used in the detergent formulations.
  • the surfactant can be anionic, non-ionic, cationic or mixture thereof.
  • Anionic surfactants can include soaps as well as non-soap detergents.
  • each of the components i.e. the first and the second component, are substantially free of surfactant.
  • Conventional detergent formulations comprise several ingredients for specific functions. Such ingredients include fluorescer, soil-release polymer, builder, bleach, and optical bleach, brightener, and particulate fillers. It is envisaged by the present inventors that one or both the components comprise ingredients used in conventional detergent formulations. It is preferred however that the first component does not comprise alkaline ingredients and the second component does not comprise acidic ingredients.
  • both the components are packaged in a variety of ways so as to make it convenient for the consumer. Accordingly, both the components may be individually packaged. Alternatively, both the components can be packaged in a two-compartment packaging such that the two components are separated from each other by a barrier material.
  • both the components When both the components are in liquid form, they can be preferably packaged in a two-compartment bottle or pouch such that the two components are separated from each other by a barrier material.
  • the packaging has individual dispensing means to allow dispensing of each of the component separately.
  • the dispensing means include spraying means for convenient local application on specific area of fabric.
  • any of the components when any of the components is in particulate solid form, it can be packaged in a sachet.
  • the sachet is for single dosage.
  • any of the components, when in solid form can be in form of a shaped solid such as a bar or stick.
  • the bar or stick form may be conveniently used for local application to fabrics.
  • the process of the present invention can be conveniently used as a hand-wash process, as it causes relatively less damage to hands as compared to the prior art methods.
  • the process can be used in the washing machines.
  • the fabric is first soaked in a container containing first component, removed from the container, and dipped into the second component.
  • the fabric is first soaked in a container containing the second component, removed from the container, and dipped into the first component.
  • the fabric is soaked in the first component comprising an organic acid and aqueous carrier, and then washed with detergent powder comprising an alkaline material.
  • the first component is sprayed on or contacted with a localized stain and then washed with a detergent powder or bar comprising an alkaline material.
  • the method can be used for pre-treatment of localized stains.
  • the fabric is sprayed with one of the components and then dipped or soaked in the other component.
  • the ratio of weight of the component that is contacted with the fabric later, to the weight of the component that is contacted with the fabric earlier is greater than 1, preferably greater than 5, more preferably greater than 10 and most preferably greater than 20.
  • the process of cleaning is carried out in a washing machine capable of sequentially releasing the two components.
  • the fabric is contacted with the first component and the second component, in any order.
  • Fabric may be contacted with the first component and followed by contacting with the second component.
  • the fabric may be contacted with the second component, and followed by contacting with the first component.
  • the alkalinity of the second component causes slimy or slippery feel resulting into usage of larger amounts of water during rinsing. It is preferred that the fabric is contacted with the second component before contacting with the first component.
  • the preferred order of contact provides an advantage of usage of relatively less water for rinsing, and also results into perception of better sensory and less damage to hands; particularly in a hand-washing process.
  • liquid to cloth ratio means the ratio of mass of liquid to the mass of fabric in contact with the liquid.
  • the liquor to cloth ratio can be anywhere from 1 to 150, during the step of contacting with any one of the components that includes aqueous carrier.
  • the liquor to cloth ratio during contact with any one of the components is preferably less than 20, more preferably less than 10 and most preferably less than 5.
  • the process according to the present invention has some advantages over the processes of the prior art.
  • the process of the present invention can be carried out at a temperature between 0-90 °C, preferably between 5-60 °C, more preferably between 10-50 °C. It is one of the advantages of the present invention that superior cleaning is obtained even at relatively low wash temperature.
  • the process of the present invention can be carried out in soft water as well as hard water. It is one of the advantages of the present invention that superior cleaning is obtained with water that has relatively high water hardness.
  • the process of the present invention can be used for removing spots or stains from a localized area of a fabric.
  • the process for cleaning fabrics according to the present invention is particularly suitable for cleaning delicate garments or accessories such as buttons, lace and elastic as it causes relatively less damage.
  • Table 1 Materials used Material Source Form used Test fabric WFK10A WFK, Germany 10 cm by 10 cm swatch Test fabric WFK10D WFK, Germany 10 cm by 10 cm swatch Particulate soil test monitor Prepared from desized cotton/ WFK10A by method described below.
  • Particulate soil composition China clay 90%, silica 5%, carbon soot (collected from diesel engine fumes) 2.5% and iron oxide 2.5%
  • the soiled fabric swatches (10 cm x 10 cm) were first treated with the first component comprising organic acid, followed by contacting with the second component comprising alkaline material. Experiments were also carried out where order of contacting was reversed, i.e. the second component was contacted with fabric and the wetted fabric was then contacted with the first component. All experiments were carried out with 5 fabric swatches and the results reported are for 5 replicates, unless specified otherwise.
  • the first component When the acid used was water soluble, the first component was in form of aqueous solution. Water insoluble acids were dissolved in chloroform. The first component was contacted with the fabric swatch by pipetting the solution on to fabric (2 mL per swatch). The wetted fabrics were then soaked in the second component (in form of aqueous solution of alkali). Sodium carbonate, sodium tripolyphosphate and mixtures thereof were used as alkali (0.1-3 g/L sodium carbonate and 0.1 - 3 g/L sodium tripolyphosphate).
  • the soaking in the second component was for a time period of 30 minutes directly in the washing pot of tergetometer (Instrument marketing services Inc., Fairfield, NJ 07004) or launderometer (Linitest) without agitation. Soaking time of 30 minutes was used in the experiments, unless specified otherwise. Wash liquor to cloth ratio (by weight) was maintained at 50 in the tergetometer. In launderometer, the wash liquor to cloth ratio (by weight) was varied from 10 to 50. The wash time duration was 15 minutes.
  • the agitation in the tergetometer was provided by a vertical spindle rotating at an angular speed of 75 RPM and in the launderometer by a tumbling mechanism at a speed of 45 RPM.
  • Reflectance of fabrics was measured as an indicator of cleaning efficacy. Reflectance measurements, at 460 nm wavelength, before and after wash were carried out with the help of Gretag Macbeth reflectometer (Color Eye 7000A). The UV component of the incident light was blocked by appropriate filter devices, built in the system, in order to avoid any possible artifacts on account of fluorescence emitted by fluorescer molecules if present on fabric. Measurements of reflectance are based on 5 swatches, and expressed as: mean ⁇ standard deviation.
  • Breaking strength of fibers was used as a measure of damage to fabrics.
  • Texture analyzer Instron Series IX (TA Instruments, TA-HDi) was used for measurement of strength of fibers. Individual fibers were drawn out from the washed fabrics. A single fiber was attached to the fixture meant for tensile strength measurement and axial tension was applied. A 5 kg load cell was used for the experiment. Care was taken so that the fiber was stretched between the load cell and the bottom fixture prior to the application of axial tension. The load cell was pulled upward at a rate of 1 mm/s till the fiber withstood the applied tension. When the applied tension exceeded that of the tensile strength of the fiber, the fiber snapped and the corresponding tension at the break was noted.
  • Example 1 is within the scope of the present invention whilst the comparative example 1-A is outside the scope of the present invention.
  • Table 2 Effect of type of acid used on cleaning efficacy
  • Example 2 is within the scope of the present invention and comparative example 2-A is outside the scope of the present invention.
  • Examples 3, 4, and 5 are within the scope of the invention and example 3-A is outside the scope of the invention.
  • Example 6 is within the scope of the invention whilst comparative examples 6-A and 6-B are examples of conventional method of cleaning using commercially available detergent powders.
  • the amount of first and second components used in example 6 and the amount of commercially available detergent powders used in examples 6-A and 6-B are chosen so that the cost of washing is identical.
  • Examples 7, 7-A and 7-B are similar to corresponding examples 6, 6-A and 6-B, respectively except that the fabric used is WFK10D.
  • Examples 12-15 demonstrate the range of molecular weights of polycarboxylic acid that can be used in the process of the present invention. It is also seen that the cleaning efficacy improves with the increase in molecular weight of acid used.
  • Examples 16-19 demonstrate the types of alkalis and concentrations thereof that can be used according to the present invention.
  • Example 19-A which is a conventional cleaning method, is outside the scope of the present invention and is a comparative example for examples 12-19.
  • Examples 20-25 are further examples according to the present invention which demonstrate superior cleaning over comparative example 25-A.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
EP07120469A 2007-08-29 2007-11-12 Processus de nettoyage de tissus Withdrawn EP2031050A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN1647MU2007 2007-08-29

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EP2031050A1 true EP2031050A1 (fr) 2009-03-04

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016066369A1 (fr) * 2014-10-29 2016-05-06 Unilever Plc Réduction de la détérioration des couleurs pendant le procédé de lavage du linge
WO2023175537A1 (fr) * 2022-03-17 2023-09-21 Diversey, Inc. Compositions synergétiques d'élimination de taches de rouille et procédés d'élimination de taches de rouille d'un tissu

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB333177A (en) * 1929-05-03 1930-08-05 Archibald Rayner Improved method of washing
DE2338411A1 (de) * 1973-07-28 1975-02-13 Henkel & Cie Gmbh Waschverfahren fuer textilien zur entfernung fettiger verschmutzungen
EP0419036A2 (fr) * 1989-08-21 1991-03-27 Unilever Plc Additif renforçateur pour détergents et système le contenant
EP1167501A1 (fr) * 2000-06-19 2002-01-02 The Procter & Gamble Company Procédé de traitement de tissus par production de chaleur
US20030060384A1 (en) * 2001-09-14 2003-03-27 Hammock Cory S. Surfactant-free cleaning compositions and processes for the use thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB333177A (en) * 1929-05-03 1930-08-05 Archibald Rayner Improved method of washing
DE2338411A1 (de) * 1973-07-28 1975-02-13 Henkel & Cie Gmbh Waschverfahren fuer textilien zur entfernung fettiger verschmutzungen
EP0419036A2 (fr) * 1989-08-21 1991-03-27 Unilever Plc Additif renforçateur pour détergents et système le contenant
EP1167501A1 (fr) * 2000-06-19 2002-01-02 The Procter & Gamble Company Procédé de traitement de tissus par production de chaleur
US20030060384A1 (en) * 2001-09-14 2003-03-27 Hammock Cory S. Surfactant-free cleaning compositions and processes for the use thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016066369A1 (fr) * 2014-10-29 2016-05-06 Unilever Plc Réduction de la détérioration des couleurs pendant le procédé de lavage du linge
WO2023175537A1 (fr) * 2022-03-17 2023-09-21 Diversey, Inc. Compositions synergétiques d'élimination de taches de rouille et procédés d'élimination de taches de rouille d'un tissu

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